2e3c89f43f3bb9d386178270200d0acce9fc8050
lrnassar
  Fri Nov 22 17:47:13 2024 -0800
Giving the UI link cronjob some love by fixing all the 301 redirects. These are the bulk of the items listed on the cron. No RM.

diff --git src/hg/makeDb/trackDb/human/dbSnp153Composite.html src/hg/makeDb/trackDb/human/dbSnp153Composite.html
index f2b863c..bacb7f4 100644
--- src/hg/makeDb/trackDb/human/dbSnp153Composite.html
+++ src/hg/makeDb/trackDb/human/dbSnp153Composite.html
@@ -128,34 +128,34 @@
     </li>
     <li><a href="https://gnomad.broadinstitute.org/" target=_blank>GnomAD genomes</a>:
       The gnomAD
       <a href="https://macarthurlab.org/2018/10/17/gnomad-v2-1/" target=_blank>v2.1</a>
       genome dataset includes 229 million SNVs and 33 million indels from 15,708 genomes
       in 9 populations.
     </li>
     <li><a href="https://esp.gs.washington.edu/" target=_blank>GoESP</a>:
       The NHLBI Grand Opportunity Exome Sequencing Project (GO-ESP) dataset contains 6503 samples
       drawn from multiple ESP cohorts and represents all of the ESP exome variant data.
     </li>
     <li><a href="https://www.geenivaramu.ee/en" target=_blank>Estonian</a>:
       Genetic variation in the Estonian population: pharmacogenomics study of
       adverse drug effects using electronic health records.
     </li>
-    <li><a href="http://www.bris.ac.uk/alspac/participants/genome/" target=_blank>ALSPAC</a>:
+    <li><a href="https://www.bristol.ac.uk/alspac/participants/genome/" target=_blank>ALSPAC</a>:
       The UK10K - Avon Longitudinal Study of Parents and Children project contains 1927 sample
       including individuals obtained from the
-      <a href="http://www.bristol.ac.uk/alspac/" target=_blank>ALSPAC population</a>.
+      <a href="https://www.bristol.ac.uk/alspac/" target=_blank>ALSPAC population</a>.
       This population contains more than 14,000 mothers enrolled during pregnancy in 1991 and 1992.
     </li>
     <li><a href="https://twinsuk.ac.uk/" target=_blank>TWINSUK</a>:
       The UK10K - TwinsUK project contains 1854 samples from the
       <a href="https://twinsuk.ac.uk/" target=_blank>Department of Twin Research and
       Genetic Epidemiology (DTR)</a>.
       The DTR dataset contains data obtained from the 11,000 identical and non-identical twins
       between the ages of 16 and 85 years old.
     </li>
     <li><a href="https://swefreq.nbis.se/dataset/SweGen" target=_blank>NorthernSweden</a>:
       Whole-genome sequenced control population in northern Sweden reveals subregional
       genetic differences.  This population consists of 300 whole genome sequenced human samples
       selected from the county of Vasterbotten in northern Sweden. To be selected for inclusion
       into the population, the individuals had to have reached at least 80 years of age and have
       no diagnosed cancer.
@@ -538,31 +538,31 @@
 The columns in the bigDbSnp/bigBed files and dbSnp153Details.tab.gz file are described in
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/lib/bigDbSnp.as"
    target=_blank>bigDbSnp.as</a> and
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/lib/dbSnpDetails.as"
    target=_blank>dbSnpDetails.as</a> respectively.
 For columns that contain lists of allele frequency data, the order of projects
 providing the data listed is as follows:
 <ol>
   <li><a href="https://www.internationalgenome.org/" target=_blank>1000Genomes</a></li>
   <li><a href="https://gnomad.broadinstitute.org/" target=_blank>GnomAD exomes</a></li>
   <li><a href="https://www.nhlbiwgs.org/" target=_blank>TOPMED</a></li>
   <li><a href="https://www.pagestudy.org/" target=_blank>PAGE STUDY</a></li>
   <li><a href="https://gnomad.broadinstitute.org/" target=_blank>GnomAD genomes</a></li>
   <li><a href="https://esp.gs.washington.edu/" target=_blank>GoESP</a></li>
   <li><a href="https://www.geenivaramu.ee/en" target=_blank>Estonian</a></li>
-  <li><a href="http://www.bris.ac.uk/alspac/participants/genome/" target=_blank>ALSPAC</a></li>
+  <li><a href="https://www.bristol.ac.uk/alspac/participants/genome/" target=_blank>ALSPAC</a></li>
   <li><a href="https://twinsuk.ac.uk/" target=_blank>TWINSUK</a></li>
   <li><a href="https://swefreq.nbis.se/dataset/SweGen" target=_blank>NorthernSweden</a></li>
   <li><a href="https://genomes.vn/" target=_blank>Vietnamese</a></li>
 </ol>
 </p><p>
 UCSC also has an
 <a href="../goldenPath/help/api.html"
    target=_blank>API</a>
 that can be used to retrieve values from a particular chromosome range.
 </p><p>
 A list of rs# IDs can be pasted/uploaded in the
 <a href="hgVai" target=_blank>Variant Annotation Integrator</a>
 tool to find out which genes (if any) the variants are located in,
 as well as functional effect such as intron, coding-synonymous, missense, frameshift, etc.
 </p><p>