geneid | 6785 |
---|---|
ensemblid | ENSG00000118402.6 |
hgncid | 14415 |
symbol | ELOVL4 |
name | ELOVL fatty acid elongase 4 |
refseq_nuc | NM_022726.4 |
refseq_prot | NP_073563.1 |
ensembl_nuc | ENST00000369816.5 |
ensembl_prot | ENSP00000358831.4 |
mane_status | MANE Select |
chr | chr6 |
start | 79914814 |
end | 79947553 |
strand | - |
ver | v1.2 |
region | chr6:79914814-79947553 |
region5000 | chr6:79909814-79952553 |
regionname0 | ELOVL4_chr6_79914814_79947553 |
regionname5000 | ELOVL4_chr6_79909814_79952553 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 314 | 258 | 78 | 55 | 90 | 10 | 23 | 68 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002 | 0/0 | 314 | 95 | 18 | 13 | 42 | 2 | 20 | 34 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0003 | 0/0 | 314 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 945 | 258 | 78 | 55 | 90 | 10 | 23 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
c0002 | 0/0 | 945 | 95 | 18 | 13 | 42 | 2 | 20 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
c0003 | 0/0 | 945 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2069 | 178 | 28 | 43 | 81 | 5 | 20 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0002 | 0/0 | 2067 | 78 | 4 | 12 | 42 | 2 | 18 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0003 | 0/0 | 2069 | 27 | 25 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0004 | 0/1 | 2069 | 22 | 2 | 8 | 3 | 4 | 4 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0005 | 0/0 | 2069 | 11 | 11 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0006 | 0/0 | 2067 | 10 | 10 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0007 | 0/0 | 2069 | 5 | 2 | 2 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0008 | 0/0 | 2069 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0009 | 0/0 | 2082 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0010 | 0/0 | 2069 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0011 | 0/0 | 2069 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0012 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0013 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0014 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0015 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0016 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0017 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0018 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0019 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0020 | 0/0 | 2069 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0021 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0022 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0023 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
t0024 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 1 | 4 | 10 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0002 | 1/0 | 15 | 1 | 0 | 10 | 2 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0003 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0005 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0006 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0008 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 945 | 258 | 78 | 55 | 90 | 10 | 23 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002 | 0/0 | 945 | 95 | 18 | 13 | 42 | 2 | 20 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0003c0003 | 0/0 | 945 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3013 | 177 | 28 | 43 | 81 | 5 | 19 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0003 | 0/0 | 3013 | 27 | 25 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0004 | 0/1 | 3013 | 22 | 2 | 8 | 3 | 4 | 4 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0005 | 0/0 | 3013 | 11 | 11 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0007 | 0/0 | 3013 | 5 | 2 | 2 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0009 | 0/0 | 3026 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0010 | 0/0 | 3013 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0011 | 0/0 | 3013 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0012 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0013 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0015 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0016 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0018 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0019 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0021 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0022 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0023 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0001c0001t0024 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002t0002 | 0/0 | 3011 | 78 | 4 | 12 | 42 | 2 | 18 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002t0006 | 0/0 | 3011 | 10 | 10 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002t0008 | 0/0 | 3013 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002t0014 | 0/0 | 3011 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002t0017 | 0/0 | 3011 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0002c0002t0020 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
a0003c0003t0001 | 0/0 | 3013 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | copy fasta | chr6 | 79909814 | 79952553 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 1 | 4 | 10 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0002 | 1/0 | 15 | 1 | 0 | 10 | 2 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0008 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0007g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0011g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0015g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0016g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0019g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0021g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0022g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0023g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0001c0001t0024g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0003 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0006 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0008g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0014g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0017g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0002c0002t0020g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0218 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0082 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0080 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00558 | hp1 | a0001 | c0001 | t0011 | g0040 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01070 | hp2 | a0001 | c0001 | t0007 | g0047 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0217 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01433 | hp2 | a0002 | c0002 | t0020 | g0107 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | IBS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01884 | hp2 | a0002 | c0002 | t0008 | g0210 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02129 | hp1 | a0001 | c0001 | t0015 | g0071 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02129 | hp2 | a0001 | c0001 | t0023 | g0170 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02257 | hp1 | a0002 | c0002 | t0008 | g0012 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02257 | hp2 | a0002 | c0002 | t0006 | g0019 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02280 | hp1 | a0002 | c0002 | t0006 | g0222 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02451 | hp1 | a0002 | c0002 | t0006 | g0224 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0156 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0095 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0052 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02895 | hp2 | a0002 | c0002 | t0008 | g0012 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0086 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02897 | hp1 | a0002 | c0002 | t0008 | g0012 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02976 | hp2 | a0002 | c0002 | t0006 | g0048 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03041 | hp2 | a0002 | c0002 | t0006 | g0019 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0055 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03209 | hp2 | a0002 | c0002 | t0006 | g0221 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03225 | hp2 | a0001 | c0001 | t0022 | g0154 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03486 | hp1 | a0002 | c0002 | t0006 | g0019 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0053 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0208 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0215 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0096 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0094 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0079 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04115 | hp2 | a0002 | c0002 | t0014 | g0059 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04184 | hp2 | a0002 | c0002 | t0017 | g0081 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0085 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04204 | hp2 | a0003 | c0003 | t0001 | g0148 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18522 | hp1 | a0002 | c0002 | t0006 | g0048 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | CHB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18906 | hp1 | a0002 | c0002 | t0006 | g0223 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18906 | hp2 | a0001 | c0001 | t0016 | g0197 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18941 | hp2 | a0001 | c0001 | t0018 | g0164 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18982 | hp1 | a0001 | c0001 | t0011 | g0040 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18987 | hp1 | a0001 | c0001 | t0021 | g0140 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19030 | hp1 | a0001 | c0001 | t0024 | g0216 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0209 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | TSI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0056 | EUR | TSI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG02559 | hp2 | a0002 | c0002 | t0006 | g0220 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0093 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0058 | REF | REF | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:79916658
|
T | C | 1 | a0002 | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
missense_variant | MODERATE | c.895A>G | p.Met299Val | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1169/3013 | 895/945 | 299/314 | chr6 | 79916658 | ||
chr6:79916753
|
A | G | 1 | a0003 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.800T>C | p.Ile267Thr | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1074/3013 | 800/945 | 267/314 | chr6 | 79916753 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:79914849
|
A | T | 1 | a0001c0001t0021 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1759T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1759 | chr6 | 79914849 | |||||
chr6:79914939
|
A | C | 5 | a0002c0002t0002a0002c0002t0006a0002c0002t0014others(2): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1669T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1669 | chr6 | 79914939 | |||||
chr6:79915057
|
T | C | 2 | a0001c0001t0005a0001c0001t0009 | 13 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1551A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1551 | chr6 | 79915057 | |||||
chr6:79915542
|
A | C | 2 | a0001c0001t0007a0001c0001t0022 | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1066T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1066 | chr6 | 79915542 | |||||
chr6:79915560
|
C | T | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1048 | chr6 | 79915560 | |||||
chr6:79915588
|
T | C | 1 | a0002c0002t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1020A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1020 | chr6 | 79915588 | |||||
chr6:79915812
|
CAT | C | 4 | a0002c0002t0002a0002c0002t0006a0002c0002t0014others(1): Show | 90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*794_*795delAT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 794 | chr6 | 79915812 | |||||
chr6:79915941
|
A | G | 5 | a0002c0002t0002a0002c0002t0006a0002c0002t0008others(2): Show | 94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*667T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 667 | chr6 | 79915941 | |||||
chr6:79915999
|
C | T | 2 | a0001c0001t0007a0001c0001t0022 | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*609G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 609 | chr6 | 79915999 | |||||
chr6:79916099
|
G | A | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*509C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 509 | chr6 | 79916099 | |||||
chr6:79916231
|
A | T | 1 | a0001c0001t0011 | 2 | HG00558.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 377 | chr6 | 79916231 | |||||
chr6:79916247
|
G | A | 2 | a0001c0001t0007a0001c0001t0022 | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 361 | chr6 | 79916247 | |||||
chr6:79916248
|
T | C | 1 | a0001c0001t0023 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 360 | chr6 | 79916248 | |||||
chr6:79916400
|
T | A | 1 | a0001c0001t0024 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 208 | chr6 | 79916400 | |||||
chr6:79916401
|
A | T | 1 | a0001c0001t0018 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 207 | chr6 | 79916401 | |||||
chr6:79916404
|
A | C | 1 | a0001c0001t0010 | 2 | HG03579.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*204T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 204 | chr6 | 79916404 | |||||
chr6:79916466
|
C | G | 5 | a0002c0002t0002a0002c0002t0006a0002c0002t0008others(2): Show | 94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 142 | chr6 | 79916466 | |||||
chr6:79916600
|
A | G | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 8 | chr6 | 79916600 | |||||
chr6:79947309
|
A | C | 1 | a0001c0001t0015 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 30 | chr6 | 79947309 | |||||
chr6:79947316
|
G | A | 1 | a0001c0001t0024 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | chr6 | 79947316 | ||||||
chr6:79947369
|
C | G | 2 | a0001c0001t0004a0002c0002t0014 | 23 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 90 | chr6 | 79947369 | |||||
chr6:79947377
|
G | A | 1 | a0001c0001t0012 | 1 | HG02886.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-98C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | chr6 | 79947377 | ||||||
chr6:79947382
|
C | G | 1 | a0001c0001t0013 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 103 | chr6 | 79947382 | |||||
chr6:79947515
|
G | A | 5 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(2): Show | 45 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-236C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 236 | chr6 | 79947515 | |||||
chr6:79947538
|
C | CGCTGCAC others(6): Show |
1 | a0001c0001t0009 | 2 | HG02723.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-272_-260dupAGACTG others(7): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 260 | chr6 | 79947538 | |||||
chr6:79947547
|
A | C | 1 | a0001c0001t0012 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-268T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 268 | chr6 | 79947547 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:79917069
|
T | C | 1 | a0001c0001t0007g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670-186A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917069 | ||||||
chr6:79917131
|
AT | A | 83 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(80): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.670-249delA | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917131 | ||||||
chr6:79917139
|
T | A | 1 | a0001c0001t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670-256A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917139 | ||||||
chr6:79917585
|
C | T | 10 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0045others(7): Show | 13 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-702G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917585 | ||||||
chr6:79917688
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.670-805C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917688 | ||||||
chr6:79917794
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.670-911A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917794 | ||||||
chr6:79917828
|
A | G | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-945T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917828 | ||||||
chr6:79917916
|
G | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.670-1033C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917916 | ||||||
chr6:79918199
|
A | G | 1 | a0001c0001t0001g0009 | 4 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1221T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918199 | ||||||
chr6:79918316
|
T | G | 1 | a0003c0003t0001g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.669+1104A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918316 | ||||||
chr6:79918435
|
C | T | 58 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(55): Show | 94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.669+985G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918435 | ||||||
chr6:79918606
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.669+814T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918606 | ||||||
chr6:79918639
|
T | C | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+781A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918639 | ||||||
chr6:79918983
|
T | A | 2 | a0002c0002t0006g0220a0002c0002t0006g0222 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.669+437A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918983 | ||||||
chr6:79919030
|
A | G | 1 | a0001c0001t0013g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.669+390T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919030 | ||||||
chr6:79919042
|
A | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(76): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.669+378T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919042 | ||||||
chr6:79919110
|
A | ACATAAAT | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.669+309_669+310ins others(7): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919110 | ||||||
chr6:79919127
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.669+293C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919127 | ||||||
chr6:79919131
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0122 | 2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.669+289A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919131 | ||||||
chr6:79919194
|
G | GCTATGTC others(313): Show |
1 | a0002c0002t0002g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.669+225_669+226ins others(320): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919194 | ||||||
chr6:79919265
|
A | T | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.669+155T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919265 | ||||||
chr6:79919290
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.669+130G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919290 | ||||||
chr6:79919362
|
T | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.669+58A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919362 | ||||||
chr6:79919369
|
TA | T | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+50delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919369 | ||||||
chr6:79919399
|
C | T | 1 | a0002c0002t0002g0102 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.669+21G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919399 | ||||||
chr6:79919638
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.542-91A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79919638 | ||||||
chr6:79919801
|
G | T | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.542-254C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79919801 | ||||||
chr6:79919924
|
G | A | 1 | a0001c0001t0016g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542-377C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79919924 | ||||||
chr6:79920128
|
T | G | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.542-581A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920128 | ||||||
chr6:79920337
|
T | G | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.542-790A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920337 | ||||||
chr6:79920411
|
A | G | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-864T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920411 | ||||||
chr6:79920569
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.542-1022C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920569 | ||||||
chr6:79920609
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0176 | 2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541+1016G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920609 | ||||||
chr6:79920669
|
T | G | 1 | a0002c0002t0006g0222 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541+956A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920669 | ||||||
chr6:79920671
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.541+954A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920671 | ||||||
chr6:79921039
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.541+586G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921039 | ||||||
chr6:79921097
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0003g0236a0001c0001t0024g0216 | 3 | HG01175.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.541+528C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921097 | ||||||
chr6:79921202
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(85): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.541+423A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921202 | ||||||
chr6:79921227
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541+398G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921227 | ||||||
chr6:79921283
|
A | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541+342T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921283 | ||||||
chr6:79921369
|
G | A | 3 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0231 | 5 | HG01109.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.541+256C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921369 | ||||||
chr6:79921456
|
T | C | 1 | a0001c0001t0001g0013 | 3 | HG01109.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.541+169A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921456 | ||||||
chr6:79921459
|
C | CA | 18 | a0001c0001t0001g0037a0001c0001t0001g0135a0001c0001t0001g0137others(15): Show | 19 | HG00597.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.541+165dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
C | CAA | 17 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0143others(14): Show | 21 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.541+164_541+165dup others(2): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CA | C | 22 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0111others(19): Show | 31 | HG00733.hp2 HG00738.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.541+165delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAA | C | 44 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(41): Show | 77 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.541+164_541+165del others(2): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAA | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(8): Show | 14 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.541+161_541+165del others(5): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAAA | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0017others(27): Show | 41 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.541+160_541+165del others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.541+156_541+165del others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0113others(3): Show | 11 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.541+155_541+165del others(11): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0112a0001c0001t0003g0234 | 2 | HG01515.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.541+154_541+165del others(12): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+153_541+165del others(13): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921459
|
CAAAAAAA others(10): Show |
C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+149_541+165del others(17): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | ||||||
chr6:79921565
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0004g0056a0001c0001t0004g0057others(1): Show | 6 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+60G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921565 | ||||||
chr6:79921869
|
G | C | 1 | a0001c0001t0007g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.370-73C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921869 | ||||||
chr6:79921913
|
G | T | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.370-117C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921913 | ||||||
chr6:79921914
|
G | C | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.370-118C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921914 | ||||||
chr6:79921961
|
TG | T | 17 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(14): Show | 27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.370-166delC | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921961 | ||||||
chr6:79922039
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.370-243G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922039 | ||||||
chr6:79922115
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.370-319G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922115 | ||||||
chr6:79922177
|
C | T | 1 | a0001c0001t0001g0033 | 2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.370-381G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922177 | ||||||
chr6:79922214
|
T | C | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.370-418A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922214 | ||||||
chr6:79922457
|
G | C | 1 | a0002c0002t0002g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.370-661C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922457 | ||||||
chr6:79922460
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.370-664T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922460 | ||||||
chr6:79922533
|
A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0175a0001c0001t0018g0164 | 4 | NA18940.hp2 NA18941.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-737T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922533 | ||||||
chr6:79922812
|
T | C | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.370-1016A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922812 | ||||||
chr6:79922854
|
GAAAC | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0190 | 3 | HG02109.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.370-1062_370-1059d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922854 | ||||||
chr6:79922904
|
A | T | 55 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(52): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.370-1108T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922904 | ||||||
chr6:79922922
|
T | G | 3 | a0001c0001t0003g0230a0001c0001t0003g0232a0001c0001t0003g0233 | 3 | HG02615.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.370-1126A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922922 | ||||||
chr6:79923074
|
C | A | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-1278G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923074 | ||||||
chr6:79923095
|
A | G | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1299T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923095 | ||||||
chr6:79923226
|
C | T | 2 | a0002c0002t0002g0098a0002c0002t0002g0101 | 2 | HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.370-1430G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923226 | ||||||
chr6:79923232
|
G | A | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1436C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923232 | ||||||
chr6:79923386
|
TGTAA | T | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.369+1562_369+1565d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923386 | ||||||
chr6:79923475
|
G | C | 17 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(14): Show | 27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+1477C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923475 | ||||||
chr6:79923493
|
T | C | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+1459A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923493 | ||||||
chr6:79923534
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1418A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923534 | ||||||
chr6:79923625
|
C | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(84): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.369+1327G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923625 | ||||||
chr6:79923714
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0174 | 3 | NA18942.hp2 NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.369+1238T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923714 | ||||||
chr6:79923895
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.369+1057G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923895 | ||||||
chr6:79923939
|
G | A | 17 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(14): Show | 27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+1013C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923939 | ||||||
chr6:79924012
|
G | GTT | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.369+938_369+939dup others(2): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924012 | ||||||
chr6:79924107
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.369+845G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924107 | ||||||
chr6:79924197
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.369+755G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924197 | ||||||
chr6:79924270
|
T | C | 1 | a0001c0001t0016g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.369+682A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924270 | ||||||
chr6:79924293
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+659G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924293 | ||||||
chr6:79924427
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.369+525A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924427 | ||||||
chr6:79924558
|
A | G | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+394T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924558 | ||||||
chr6:79924565
|
G | A | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.369+387C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924565 | ||||||
chr6:79924711
|
C | T | 1 | a0001c0001t0022g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369+241G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924711 | ||||||
chr6:79924752
|
T | C | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.369+200A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924752 | ||||||
chr6:79924805
|
A | G | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.369+147T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924805 | ||||||
chr6:79924896
|
G | A | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+56C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924896 | ||||||
chr6:79925131
|
A | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(76): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.289-99T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925131 | ||||||
chr6:79925413
|
A | T | 1 | a0001c0001t0007g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289-381T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925413 | ||||||
chr6:79925514
|
G | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0174 | 3 | NA18942.hp2 NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.289-482C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925514 | ||||||
chr6:79925523
|
C | G | 78 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(75): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.289-491G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925523 | ||||||
chr6:79925568
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.289-536A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925568 | ||||||
chr6:79925735
|
T | C | 7 | a0002c0002t0006g0019a0002c0002t0006g0048a0002c0002t0006g0220others(4): Show | 10 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.288+459A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925735 | ||||||
chr6:79925878
|
G | A | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.288+316C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925878 | ||||||
chr6:79925917
|
C | T | 58 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(55): Show | 94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.288+277G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925917 | ||||||
chr6:79926005
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(84): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.288+189G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79926005 | ||||||
chr6:79926385
|
T | C | 2 | a0001c0001t0010g0208a0001c0001t0010g0209 | 2 | HG03579.hp1 NA19030.hp2 |
splice_region_variant&intron_variant | LOW | c.101-4A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926385 | ||||||
chr6:79926472
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.101-91A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926472 | ||||||
chr6:79926538
|
C | A | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.101-157G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926538 | ||||||
chr6:79926649
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0145others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-268G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926649 | ||||||
chr6:79926665
|
G | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-284C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926665 | ||||||
chr6:79926684
|
A | T | 56 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(53): Show | 90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-303T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926684 | ||||||
chr6:79926837
|
G | A | 56 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(53): Show | 90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-456C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926837 | ||||||
chr6:79926906
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.101-525A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926906 | ||||||
chr6:79927046
|
C | T | 3 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0231 | 5 | HG01109.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-665G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927046 | ||||||
chr6:79927243
|
C | T | 1 | a0001c0001t0004g0021 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.101-862G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927243 | ||||||
chr6:79927337
|
T | C | 1 | a0001c0001t0001g0013 | 3 | HG01109.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.101-956A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927337 | ||||||
chr6:79927350
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.101-969T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927350 | ||||||
chr6:79927354
|
C | T | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-973G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927354 | ||||||
chr6:79927355
|
G | A | 2 | a0001c0001t0010g0208a0001c0001t0010g0209 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-974C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927355 | ||||||
chr6:79927432
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0189 | 3 | HG01074.hp1 HG01192.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.101-1051G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927432 | ||||||
chr6:79927447
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0145 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.101-1066A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927447 | ||||||
chr6:79927521
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.101-1140C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927521 | ||||||
chr6:79927522
|
T | C | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-1141A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927522 | ||||||
chr6:79927593
|
G | A | 56 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(53): Show | 90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-1212C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927593 | ||||||
chr6:79927629
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.101-1248C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927629 | ||||||
chr6:79927780
|
CAT | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-1401_101-1400d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927780 | ||||||
chr6:79927818
|
T | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1437A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927818 | ||||||
chr6:79928041
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101-1660A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928041 | ||||||
chr6:79928098
|
C | A | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-1717G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928098 | ||||||
chr6:79928224
|
C | A | 170 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0013others(167): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.101-1843G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928224 | ||||||
chr6:79928348
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(84): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.101-1967G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928348 | ||||||
chr6:79928358
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-1977A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928358 | ||||||
chr6:79928364
|
A | C | 1 | a0001c0001t0001g0009 | 4 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1983T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928364 | ||||||
chr6:79928403
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-2022G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928403 | ||||||
chr6:79928423
|
G | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2042C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928423 | ||||||
chr6:79928426
|
T | A | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-2045A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928426 | ||||||
chr6:79928516
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0142a0001c0001t0004g0066others(1): Show | 5 | HG00733.hp1 HG01106.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-2135A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928516 | ||||||
chr6:79928626
|
T | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-2245A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928626 | ||||||
chr6:79928636
|
T | C | 56 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(53): Show | 90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-2255A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928636 | ||||||
chr6:79928727
|
G | GT | 51 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0016others(48): Show | 68 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.101-2347dupA | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928727
|
G | GTT | 23 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0113others(20): Show | 27 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-2348_101-2347d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928727
|
G | GTTT | 7 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0151others(4): Show | 10 | HG00738.hp1 HG00741.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-2349_101-2347d others(5): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928727
|
G | GTTTT | 29 | a0001c0001t0001g0149a0001c0001t0001g0150a0002c0002t0002g0003others(26): Show | 55 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.101-2350_101-2347d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928727
|
G | GTTTTT | 23 | a0001c0001t0003g0051a0001c0001t0003g0227a0001c0001t0003g0231others(20): Show | 30 | HG00733.hp2 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-2351_101-2347d others(7): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928727
|
G | GTTTTTT | 16 | a0001c0001t0001g0111a0001c0001t0003g0007a0001c0001t0003g0011others(13): Show | 25 | HG01891.hp2 HG01981.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.101-2352_101-2347d others(8): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928727
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101-2356_101-2347d others(12): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | ||||||
chr6:79928742
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-2361A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928742 | ||||||
chr6:79928755
|
T | TA | 4 | a0001c0001t0001g0126a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | NA18940.hp1 NA18994.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2375dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928755 | ||||||
chr6:79928770
|
C | G | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2389G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928770 | ||||||
chr6:79928847
|
C | T | 1 | a0001c0001t0004g0067 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.101-2466G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928847 | ||||||
chr6:79928952
|
C | T | 17 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(14): Show | 27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-2571G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928952 | ||||||
chr6:79928984
|
C | A | 1 | a0002c0002t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.101-2603G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928984 | ||||||
chr6:79929125
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-2744C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929125 | ||||||
chr6:79929169
|
AG | A | 56 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(53): Show | 90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-2789delC | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929169 | ||||||
chr6:79929310
|
C | T | 24 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0073others(21): Show | 31 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-2929G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929310 | ||||||
chr6:79929354
|
C | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02015.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.101-2973G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929354 | ||||||
chr6:79929389
|
C | T | 75 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(72): Show | 120 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.101-3008G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929389 | ||||||
chr6:79929411
|
T | C | 1 | a0001c0001t0016g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-3030A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929411 | ||||||
chr6:79929429
|
C | G | 1 | a0001c0001t0003g0228 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.101-3048G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929429 | ||||||
chr6:79929604
|
T | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0017others(33): Show | 49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.101-3223A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929604 | ||||||
chr6:79929732
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-3351C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929732 | ||||||
chr6:79929797
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.101-3416G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929797 | ||||||
chr6:79929799
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101-3418T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929799 | ||||||
chr6:79929881
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101-3500A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929881 | ||||||
chr6:79930000
|
C | T | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-3619G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930000 | ||||||
chr6:79930073
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(84): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.101-3692G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930073 | ||||||
chr6:79930105
|
C | T | 2 | a0001c0001t0010g0208a0001c0001t0010g0209 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-3724G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930105 | ||||||
chr6:79930249
|
A | T | 1 | a0002c0002t0002g0076 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.101-3868T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930249 | ||||||
chr6:79930446
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0018g0164 | 3 | NA18940.hp2 NA18941.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.101-4065G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930446 | ||||||
chr6:79930592
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-4211A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930592 | ||||||
chr6:79930613
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.101-4232G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930613 | ||||||
chr6:79930676
|
G | T | 8 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0045others(5): Show | 11 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-4295C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930676 | ||||||
chr6:79931130
|
G | A | 36 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0073others(33): Show | 46 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.101-4749C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931130 | ||||||
chr6:79931154
|
T | C | 1 | a0001c0001t0005g0206 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.101-4773A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931154 | ||||||
chr6:79931234
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-4853C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931234 | ||||||
chr6:79931294
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-4913G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931294 | ||||||
chr6:79931384
|
G | A | 1 | a0001c0001t0004g0067 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.101-5003C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931384 | ||||||
chr6:79931437
|
C | G | 10 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0045others(7): Show | 13 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.101-5056G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931437 | ||||||
chr6:79931689
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-5308C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931689 | ||||||
chr6:79931715
|
G | GA | 2 | a0001c0001t0001g0030a0001c0001t0001g0129 | 3 | HG00642.hp1 HG01123.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.101-5335dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931715 | ||||||
chr6:79931785
|
A | T | 1 | a0002c0002t0006g0048 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.101-5404T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931785 | ||||||
chr6:79931806
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-5425A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931806 | ||||||
chr6:79931986
|
T | G | 3 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0231 | 5 | HG01109.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-5605A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931986 | ||||||
chr6:79932328
|
G | T | 19 | a0002c0002t0002g0004a0002c0002t0002g0006a0002c0002t0002g0022others(16): Show | 34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.101-5947C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932328 | ||||||
chr6:79932438
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-6057C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932438 | ||||||
chr6:79932529
|
G | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6148C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932529 | ||||||
chr6:79932551
|
C | CA | 19 | a0001c0001t0001g0111a0001c0001t0001g0136a0001c0001t0001g0137others(16): Show | 29 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.101-6171dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932551 | ||||||
chr6:79932551
|
C | CAA | 58 | a0001c0001t0003g0232a0001c0001t0003g0233a0002c0002t0002g0003others(55): Show | 92 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.101-6172_101-6171d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932551 | ||||||
chr6:79932564
|
T | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101-6183A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932564 | ||||||
chr6:79932566
|
G | A | 1 | a0001c0001t0007g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.101-6185C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932566 | ||||||
chr6:79932842
|
TG | T | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-6462delC | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932842 | ||||||
chr6:79932862
|
G | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6481C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932862 | ||||||
chr6:79932870
|
G | T | 2 | a0001c0001t0009g0053a0001c0001t0009g0054 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.101-6489C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932870 | ||||||
chr6:79932892
|
CTT | C | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-6513_101-6512d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932892 | ||||||
chr6:79932948
|
C | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(76): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-6567G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932948 | ||||||
chr6:79933045
|
T | C | 1 | a0001c0001t0001g0041 | 2 | HG01081.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.101-6664A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933045 | ||||||
chr6:79933220
|
T | G | 1 | a0002c0002t0006g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-6839A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933220 | ||||||
chr6:79933220
|
T | TTTTG | 20 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(17): Show | 32 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.101-6843_101-6840d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933220 | ||||||
chr6:79933220
|
TTTTGTTT others(1): Show |
T | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-6847_101-6840d others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933220 | ||||||
chr6:79933328
|
G | T | 79 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(76): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-6947C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933328 | ||||||
chr6:79933333
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.101-6952G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933333 | ||||||
chr6:79933419
|
C | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0017others(69): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.101-7038G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933419 | ||||||
chr6:79933569
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101-7188C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933569 | ||||||
chr6:79933833
|
A | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(76): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-7452T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933833 | ||||||
chr6:79933957
|
T | C | 17 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(14): Show | 27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-7576A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933957 | ||||||
chr6:79934259
|
G | A | 20 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-7878C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934259 | ||||||
chr6:79934320
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-7939C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934320 | ||||||
chr6:79934336
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-7955C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934336 | ||||||
chr6:79934457
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.101-8076C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934457 | ||||||
chr6:79934698
|
C | G | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8317G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934698 | ||||||
chr6:79934738
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.101-8357A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934738 | ||||||
chr6:79934773
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-8392T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934773 | ||||||
chr6:79934809
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.101-8428T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934809 | ||||||
chr6:79934972
|
A | C | 1 | a0002c0002t0002g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.101-8591T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934972 | ||||||
chr6:79935105
|
T | C | 16 | a0002c0002t0002g0003a0002c0002t0002g0014a0002c0002t0002g0084others(13): Show | 30 | HG00423.hp1 HG00609.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.101-8724A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935105 | ||||||
chr6:79935167
|
C | T | 78 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(75): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.101-8786G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935167 | ||||||
chr6:79935314
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.101-8933A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935314 | ||||||
chr6:79935462
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-9081C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935462 | ||||||
chr6:79935524
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101-9143T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935524 | ||||||
chr6:79935743
|
T | A | 58 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(55): Show | 94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.101-9362A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935743 | ||||||
chr6:79935788
|
T | C | 1 | a0001c0001t0016g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-9407A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935788 | ||||||
chr6:79935885
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0186 | 3 | HG00423.hp2 HG00609.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.101-9504A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935885 | ||||||
chr6:79936017
|
G | T | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-9636C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936017 | ||||||
chr6:79936044
|
G | A | 1 | a0002c0002t0002g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.101-9663C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936044 | ||||||
chr6:79936059
|
G | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(84): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.101-9678C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936059 | ||||||
chr6:79936502
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-10121T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936502 | ||||||
chr6:79936623
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0003g0236a0001c0001t0024g0216 | 3 | HG01175.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.101-10242G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936623 | ||||||
chr6:79936642
|
T | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(76): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-10261A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936642 | ||||||
chr6:79936807
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+10373G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936807 | ||||||
chr6:79936825
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+10355T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936825 | ||||||
chr6:79936898
|
T | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+10282A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936898 | ||||||
chr6:79937000
|
G | C | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.100+10180C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937000 | ||||||
chr6:79937056
|
A | C | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+10124T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937056 | ||||||
chr6:79937087
|
C | A | 3 | a0002c0002t0002g0025a0002c0002t0002g0026a0002c0002t0002g0083 | 5 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+10093G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937087 | ||||||
chr6:79937165
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100+10015G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937165 | ||||||
chr6:79937175
|
A | G | 84 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(81): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.100+10005T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937175 | ||||||
chr6:79937220
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+9960T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937220 | ||||||
chr6:79937274
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+9906C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937274 | ||||||
chr6:79937462
|
G | T | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+9718C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937462 | ||||||
chr6:79937550
|
G | A | 2 | a0001c0001t0010g0208a0001c0001t0010g0209 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.100+9630C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937550 | ||||||
chr6:79937568
|
G | A | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.100+9612C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937568 | ||||||
chr6:79937595
|
C | T | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9585G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937595 | ||||||
chr6:79937618
|
T | TAG | 8 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0045others(5): Show | 11 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+9560_100+9561d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937618 | ||||||
chr6:79937665
|
G | T | 8 | a0001c0001t0001g0111a0001c0001t0003g0007a0001c0001t0003g0011others(5): Show | 16 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+9515C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937665 | ||||||
chr6:79937829
|
T | C | 1 | a0003c0003t0001g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.100+9351A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937829 | ||||||
chr6:79937905
|
A | G | 3 | a0001c0001t0003g0235a0001c0001t0004g0021a0001c0001t0004g0062 | 4 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9275T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937905 | ||||||
chr6:79937936
|
C | T | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9244G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937936 | ||||||
chr6:79937944
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0112 | 5 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+9236C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937944 | ||||||
chr6:79937983
|
C | A | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9197G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937983 | ||||||
chr6:79938455
|
G | T | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+8725C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938455 | ||||||
chr6:79938468
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100+8712A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938468 | ||||||
chr6:79938628
|
T | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+8552A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938628 | ||||||
chr6:79938799
|
C | T | 1 | a0002c0002t0002g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8381G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938799 | ||||||
chr6:79938802
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.100+8378A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938802 | ||||||
chr6:79938813
|
A | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(85): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.100+8367T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938813 | ||||||
chr6:79938960
|
C | A | 1 | a0001c0001t0007g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.100+8220G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938960 | ||||||
chr6:79938970
|
G | A | 83 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(80): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.100+8210C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938970 | ||||||
chr6:79939042
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100+8138A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939042 | ||||||
chr6:79939142
|
C | T | 1 | a0002c0002t0002g0091 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100+8038G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939142 | ||||||
chr6:79939390
|
C | G | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+7790G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939390 | ||||||
chr6:79939419
|
T | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+7761A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939419 | ||||||
chr6:79939455
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+7725T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939455 | ||||||
chr6:79939503
|
C | CTTTA | 76 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(73): Show | 104 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.100+7673_100+7676d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | ||||||
chr6:79939503
|
C | CTTTATTT others(1): Show |
16 | a0001c0001t0001g0139a0001c0001t0004g0068a0001c0001t0005g0044others(13): Show | 24 | HG00323.hp2 HG00733.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+7669_100+7676d others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | ||||||
chr6:79939503
|
C | CTTTATTT others(5): Show |
3 | a0001c0001t0001g0153a0001c0001t0005g0045a0001c0001t0005g0206 | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+7665_100+7676d others(14): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | ||||||
chr6:79939503
|
CTTTA | C | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+7673_100+7676d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | ||||||
chr6:79939503
|
CTTTATTT others(5): Show |
C | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+7665_100+7676d others(14): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | ||||||
chr6:79939680
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.100+7500C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939680 | ||||||
chr6:79939712
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(85): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.100+7468A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939712 | ||||||
chr6:79939732
|
T | C | 17 | a0001c0001t0001g0111a0001c0001t0001g0214a0001c0001t0003g0007others(14): Show | 27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.100+7448A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939732 | ||||||
chr6:79939997
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+7183T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939997 | ||||||
chr6:79940005
|
C | T | 127 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(124): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.100+7175G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940005 | ||||||
chr6:79940166
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.100+7014A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940166 | ||||||
chr6:79940300
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+6880G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940300 | ||||||
chr6:79940314
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+6866T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940314 | ||||||
chr6:79940317
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+6863A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940317 | ||||||
chr6:79940374
|
T | C | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+6806A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940374 | ||||||
chr6:79940394
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0003g0011a0001c0001t0003g0225others(1): Show | 7 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6786C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940394 | ||||||
chr6:79940405
|
T | C | 2 | a0002c0002t0008g0012a0002c0002t0008g0210 | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6775A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940405 | ||||||
chr6:79940453
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0190 | 3 | HG02109.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+6727G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940453 | ||||||
chr6:79940663
|
T | C | 1 | a0002c0002t0002g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.100+6517A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940663 | ||||||
chr6:79940676
|
G | A | 1 | a0001c0001t0005g0206 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100+6504C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940676 | ||||||
chr6:79940694
|
A | G | 84 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(81): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.100+6486T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940694 | ||||||
chr6:79940742
|
C | T | 2 | a0001c0001t0001g0159a0002c0002t0002g0086 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.100+6438G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940742 | ||||||
chr6:79940829
|
T | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0132others(2): Show | 7 | HG02129.hp1 NA18962.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6351A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940829 | ||||||
chr6:79940929
|
A | AGAC | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+6248_100+6250d others(5): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940929 | ||||||
chr6:79941012
|
TA | T | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0073others(20): Show | 30 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+6167delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941012 | ||||||
chr6:79941147
|
T | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0190 | 3 | HG02109.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+6033A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941147 | ||||||
chr6:79941153
|
G | A | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+6027C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941153 | ||||||
chr6:79941154
|
A | G | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+6026T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941154 | ||||||
chr6:79941583
|
C | T | 1 | a0002c0002t0002g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100+5597G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941583 | ||||||
chr6:79941598
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.100+5582C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941598 | ||||||
chr6:79941678
|
A | T | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+5502T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941678 | ||||||
chr6:79941711
|
C | A | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+5469G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941711 | ||||||
chr6:79941712
|
A | C | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+5468T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941712 | ||||||
chr6:79941771
|
T | C | 1 | a0001c0001t0003g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+5409A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941771 | ||||||
chr6:79941861
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.100+5319C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941861 | ||||||
chr6:79941894
|
T | C | 1 | a0001c0001t0016g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100+5286A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941894 | ||||||
chr6:79941899
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+5281T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941899 | ||||||
chr6:79941961
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+5219A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941961 | ||||||
chr6:79942084
|
G | C | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5096C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942084 | ||||||
chr6:79942185
|
G | C | 19 | a0002c0002t0002g0004a0002c0002t0002g0006a0002c0002t0002g0022others(16): Show | 34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+4995C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942185 | ||||||
chr6:79942226
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.100+4954G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942226 | ||||||
chr6:79942245
|
C | T | 1 | a0001c0001t0003g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+4935G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942245 | ||||||
chr6:79942356
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+4824A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942356 | ||||||
chr6:79942414
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+4766A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942414 | ||||||
chr6:79942512
|
G | T | 78 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0111others(75): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+4668C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942512 | ||||||
chr6:79942760
|
A | T | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+4420T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942760 | ||||||
chr6:79942846
|
G | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+4334C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942846 | ||||||
chr6:79942952
|
G | A | 8 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0045others(5): Show | 11 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+4228C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942952 | ||||||
chr6:79943176
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+4004A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943176 | ||||||
chr6:79943228
|
G | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+3952C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943228 | ||||||
chr6:79943437
|
C | G | 4 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0212others(1): Show | 4 | HG00741.hp1 HG02055.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+3743G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943437 | ||||||
chr6:79943442
|
A | G | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(54): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.100+3738T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943442 | ||||||
chr6:79943460
|
G | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.100+3720C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943460 | ||||||
chr6:79943461
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.100+3719C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943461 | ||||||
chr6:79943465
|
A | C | 1 | a0001c0001t0003g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+3715T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943465 | ||||||
chr6:79943549
|
G | A | 1 | a0002c0002t0002g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+3631C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943549 | ||||||
chr6:79943656
|
C | A | 19 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(16): Show | 30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+3524G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943656 | ||||||
chr6:79943674
|
A | C | 59 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(56): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+3506T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943674 | ||||||
chr6:79943778
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0112others(1): Show | 9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+3402G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943778 | ||||||
chr6:79943820
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.100+3360A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943820 | ||||||
chr6:79943925
|
A | G | 78 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(75): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+3255T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943925 | ||||||
chr6:79943933
|
A | G | 78 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0190others(75): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+3247T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943933 | ||||||
chr6:79943941
|
GAA | G | 19 | a0002c0002t0002g0004a0002c0002t0002g0006a0002c0002t0002g0022others(16): Show | 34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+3237_100+3238d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943941 | ||||||
chr6:79944200
|
A | T | 1 | a0002c0002t0002g0084 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+2980T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944200 | ||||||
chr6:79944388
|
A | G | 1 | a0001c0001t0001g0033 | 2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.100+2792T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944388 | ||||||
chr6:79944916
|
T | C | 170 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0013others(167): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.100+2264A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944916 | ||||||
chr6:79944929
|
C | T | 5 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(2): Show | 6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+2251G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944929 | ||||||
chr6:79944987
|
C | CA | 15 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0199others(12): Show | 22 | HG00741.hp1 HG01257.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.100+2192dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | ||||||
chr6:79944987
|
CA | C | 38 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(35): Show | 45 | HG00280.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.100+2192delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | ||||||
chr6:79944987
|
CAA | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0017others(27): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.100+2191_100+2192d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | ||||||
chr6:79944987
|
CAAAAAAA others(1): Show |
C | 59 | a0001c0001t0001g0072a0001c0001t0004g0061a0002c0002t0002g0003others(56): Show | 93 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.100+2185_100+2192d others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | ||||||
chr6:79944987
|
CAAAAAAA others(3): Show |
C | 22 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(19): Show | 38 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.100+2183_100+2192d others(12): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | ||||||
chr6:79945133
|
A | G | 1 | a0002c0002t0002g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+2047T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945133 | ||||||
chr6:79945224
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.100+1956C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945224 | ||||||
chr6:79945282
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0004g0060 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.100+1898T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945282 | ||||||
chr6:79945707
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.100+1473T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945707 | ||||||
chr6:79945797
|
C | CA | 62 | a0001c0001t0001g0072a0001c0001t0001g0211a0001c0001t0010g0208others(59): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.100+1382dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945797 | ||||||
chr6:79945834
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100+1346C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945834 | ||||||
chr6:79946164
|
G | A | 1 | a0002c0002t0002g0213 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100+1016C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946164 | ||||||
chr6:79946381
|
T | C | 1 | a0001c0001t0001g0046 | 2 | HG00609.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.100+799A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946381 | ||||||
chr6:79946392
|
A | G | 19 | a0001c0001t0001g0074a0002c0002t0002g0004a0002c0002t0002g0006others(16): Show | 34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+788T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946392 | ||||||
chr6:79946394
|
GA | G | 56 | a0001c0001t0001g0013a0001c0001t0001g0074a0002c0002t0002g0003others(53): Show | 92 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.100+785delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946394 | ||||||
chr6:79946511
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0004g0056a0001c0001t0004g0057others(1): Show | 4 | HG00558.hp2 HG01515.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+669G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946511 | ||||||
chr6:79946516
|
C | G | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+664G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946516 | ||||||
chr6:79946670
|
C | G | 2 | a0001c0001t0009g0053a0001c0001t0009g0054 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.100+510G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946670 | ||||||
chr6:79946714
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100+466C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946714 | ||||||
chr6:79946798
|
A | C | 2 | a0001c0001t0012g0052a0002c0002t0008g0012 | 4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+382T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946798 | ||||||
chr6:79946972
|
C | A | 1 | a0002c0002t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100+208G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946972 | ||||||
chr6:79947028
|
C | T | 4 | a0001c0001t0007g0047a0001c0001t0007g0217a0001c0001t0007g0218others(1): Show | 5 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+152G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79947028 |