geneid | 79993 |
---|---|
ensemblid | ENSG00000164181.14 |
hgncid | 26292 |
symbol | ELOVL7 |
name | ELOVL fatty acid elongase 7 |
refseq_nuc | NM_024930.3 |
refseq_prot | NP_079206.2 |
ensembl_nuc | ENST00000508821.6 |
ensembl_prot | ENSP00000424123.1 |
mane_status | MANE Select |
chr | chr5 |
start | 60751791 |
end | 60844269 |
strand | - |
ver | v1.2 |
region | chr5:60751791-60844269 |
region5000 | chr5:60746791-60849269 |
regionname0 | ELOVL7_chr5_60751791_60844269 |
regionname5000 | ELOVL7_chr5_60746791_60849269 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 281 | 255 | 80 | 46 | 79 | 16 | 32 | 58 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0002 | 0/0 | 281 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0003 | 0/0 | 281 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 846 | 254 | 79 | 46 | 79 | 16 | 32 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
c0002 | 0/0 | 846 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
c0003 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
c0004 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3029 | 73 | 11 | 16 | 32 | 6 | 7 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0002 | 0/0 | 3029 | 47 | 2 | 5 | 30 | 0 | 10 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0003 | 0/0 | 3029 | 43 | 34 | 2 | 2 | 3 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0004 | 0/0 | 3030 | 23 | 0 | 3 | 16 | 2 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0005 | 0/0 | 3029 | 18 | 6 | 7 | 0 | 3 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0006 | 0/0 | 3030 | 12 | 10 | 0 | 0 | 0 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0007 | 0/0 | 3029 | 9 | 0 | 3 | 0 | 1 | 5 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0008 | 0/0 | 3029 | 8 | 8 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0009 | 1/0 | 3029 | 4 | 0 | 2 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0010 | 0/0 | 3029 | 4 | 0 | 3 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0011 | 0/0 | 3029 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0012 | 0/0 | 3029 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0013 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0014 | 0/0 | 3029 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0015 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0016 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0017 | 0/0 | 3029 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0018 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0019 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0020 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0021 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0022 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0023 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0024 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
t0025 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 846 | 254 | 79 | 46 | 79 | 16 | 32 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0003 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0002c0002 | 0/0 | 846 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0003c0004 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3874 | 71 | 11 | 16 | 30 | 6 | 7 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0002 | 0/0 | 3874 | 46 | 2 | 5 | 29 | 0 | 10 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0003 | 0/0 | 3874 | 43 | 34 | 2 | 2 | 3 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0004 | 0/0 | 3875 | 23 | 0 | 3 | 16 | 2 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0005 | 0/0 | 3874 | 18 | 6 | 7 | 0 | 3 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0006 | 0/0 | 3875 | 11 | 9 | 0 | 0 | 0 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0007 | 0/0 | 3874 | 9 | 0 | 3 | 0 | 1 | 5 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0008 | 0/0 | 3874 | 8 | 8 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0009 | 1/0 | 3874 | 4 | 0 | 2 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0010 | 0/0 | 3874 | 4 | 0 | 3 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0011 | 0/0 | 3874 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0012 | 0/0 | 3874 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0013 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0014 | 0/0 | 3874 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0015 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0016 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0017 | 0/0 | 3874 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0018 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0019 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0020 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0021 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0022 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0023 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0024 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0001t0025 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0001c0003t0006 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0002c0002t0001 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0002c0002t0002 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
a0003c0004t0001 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | copy fasta | chr5 | 60746791 | 60849269 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0011g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0012g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0012g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0014g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0017g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0019g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0021g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0022g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0023g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0024g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0025g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0003t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0003c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0176 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0009 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0246 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0031 | EUR | FIN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00735 | hp1 | a0001 | c0001 | t0010 | g0247 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0250 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01074 | hp2 | a0001 | c0001 | t0010 | g0248 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01099 | hp2 | a0001 | c0001 | t0014 | g0024 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0203 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01175 | hp2 | a0001 | c0001 | t0023 | g0164 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01192 | hp1 | a0001 | c0001 | t0012 | g0243 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0034 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01261 | hp2 | a0001 | c0001 | t0010 | g0251 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01433 | hp1 | a0001 | c0001 | t0012 | g0244 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0032 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0112 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0182 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0010 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0181 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01981 | hp1 | a0001 | c0001 | t0009 | g0245 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01981 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0130 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02615 | hp1 | a0001 | c0001 | t0025 | g0163 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0135 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02717 | hp1 | a0001 | c0001 | t0022 | g0174 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0165 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02809 | hp1 | a0001 | c0003 | t0006 | g0141 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0007 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02896 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0133 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0202 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0137 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0033 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03579 | hp2 | a0001 | c0001 | t0021 | g0196 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0252 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0028 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0030 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0204 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04228 | hp1 | a0001 | c0001 | t0017 | g0035 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18978 | hp1 | a0001 | c0001 | t0024 | g0217 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19000 | hp2 | a0001 | c0001 | t0019 | g0041 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19030 | hp1 | a0001 | c0001 | t0018 | g0039 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19063 | hp2 | a0003 | c0004 | t0001 | g0085 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20129 | hp1 | a0001 | c0001 | t0016 | g0029 | AFR | ASW | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | ASW | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0117 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0013 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | GIH | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0205 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0198 | REF | REF | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0249 | REF | REF | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60754695
|
G | A | 1 | a0002 | 2 | HG00544.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.775C>T | p.Arg259Cys | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 970/3874 | 775/846 | 259/281 | chr5 | 60754695 | ||
chr5:60771949
|
G | A | 1 | a0003 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.209C>T | p.Thr70Met | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/9 | 404/3874 | 209/846 | 70/281 | chr5 | 60771949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60772059
|
C | T | 1 | a0001c0003 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.99G>A | p.Ser33Ser | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/9 | 294/3874 | 99/846 | 33/281 | chr5 | 60772059 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60751935
|
A | C | 1 | a0001c0001t0017 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2689T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2689 | chr5 | 60751935 | |||||
chr5:60751945
|
T | C | 1 | a0001c0001t0021 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2679A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2679 | chr5 | 60751945 | |||||
chr5:60751988
|
T | C | 2 | a0001c0001t0013a0001c0001t0022 | 2 | HG02717.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2636A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2636 | chr5 | 60751988 | |||||
chr5:60752051
|
A | G | 2 | a0001c0001t0020a0001c0001t0021 | 2 | HG02572.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2573T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2573 | chr5 | 60752051 | |||||
chr5:60752147
|
T | A | 5 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(2): Show | 60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2477A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2477 | chr5 | 60752147 | |||||
chr5:60752201
|
G | A | 5 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(2): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2423C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2423 | chr5 | 60752201 | |||||
chr5:60752428
|
T | C | 1 | a0001c0001t0023 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2196 | chr5 | 60752428 | |||||
chr5:60752601
|
T | C | 1 | a0001c0001t0024 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2023 | chr5 | 60752601 | |||||
chr5:60752846
|
G | A | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1778 | chr5 | 60752846 | |||||
chr5:60752909
|
C | A | 1 | a0001c0001t0014 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1715 | chr5 | 60752909 | |||||
chr5:60752945
|
G | GA | 3 | a0001c0001t0006a0001c0001t0023a0001c0003t0006 | 13 | HG01175.hp2 HG02615.hp2 HG02647.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1678dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1678 | chr5 | 60752945 | |||||
chr5:60752952
|
A | AT | 2 | a0001c0001t0004a0001c0001t0016 | 24 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1671 | chr5 | 60752952 | |||||
chr5:60753047
|
A | G | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1577 | chr5 | 60753047 | |||||
chr5:60753292
|
T | C | 3 | a0001c0001t0003a0001c0001t0011a0001c0001t0015 | 46 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1332A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1332 | chr5 | 60753292 | |||||
chr5:60753413
|
G | A | 1 | a0001c0001t0008 | 8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1211C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1211 | chr5 | 60753413 | |||||
chr5:60753750
|
G | C | 5 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(2): Show | 60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*874C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 874 | chr5 | 60753750 | |||||
chr5:60753926
|
G | A | 1 | a0001c0001t0011 | 2 | HG01109.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 698 | chr5 | 60753926 | |||||
chr5:60754220
|
C | T | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 404 | chr5 | 60754220 | |||||
chr5:60754266
|
C | A | 1 | a0001c0001t0025 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 358 | chr5 | 60754266 | |||||
chr5:60844188
|
G | A | 1 | a0001c0001t0012 | 2 | HG01192.hp1 HG01433.hp1 |
5_prime_UTR_variant | MODIFIER | c.-114C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56791 | chr5 | 60844188 | |||||
chr5:60844234
|
T | C | 3 | a0001c0001t0007a0001c0001t0016a0001c0001t0017 | 11 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-160A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56837 | chr5 | 60844234 | |||||
chr5:60844250
|
C | T | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
5_prime_UTR_variant | MODIFIER | c.-176G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56853 | chr5 | 60844250 | |||||
chr5:60844259
|
G | T | 7 | a0001c0001t0005a0001c0001t0007a0001c0001t0013others(4): Show | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-185C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56862 | chr5 | 60844259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60755410
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.637-577C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755410 | ||||||
chr5:60755514
|
G | A | 2 | a0001c0001t0001g0088a0003c0004t0001g0085 | 2 | NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.637-681C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755514 | ||||||
chr5:60755595
|
T | G | 1 | a0001c0001t0003g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.637-762A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755595 | ||||||
chr5:60755773
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-940C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755773 | ||||||
chr5:60755912
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637-1079A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755912 | ||||||
chr5:60756010
|
T | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-1177A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756010 | ||||||
chr5:60756132
|
AG | A | 48 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(45): Show | 49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.637-1300delC | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756132 | ||||||
chr5:60756181
|
A | C | 1 | a0001c0001t0002g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.636+1328T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756181 | ||||||
chr5:60756245
|
TAAATAC | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+1258_636+1263d others(8): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756245 | ||||||
chr5:60756423
|
A | T | 1 | a0001c0001t0003g0006 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.636+1086T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756423 | ||||||
chr5:60756575
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.636+934A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756575 | ||||||
chr5:60756742
|
C | A | 44 | a0001c0001t0003g0006a0001c0001t0003g0038a0001c0001t0003g0050others(41): Show | 45 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.636+767G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756742 | ||||||
chr5:60756792
|
A | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.636+717T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756792 | ||||||
chr5:60756816
|
G | A | 90 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(87): Show | 93 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.636+693C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756816 | ||||||
chr5:60756829
|
A | T | 1 | a0001c0001t0004g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.636+680T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756829 | ||||||
chr5:60757103
|
T | C | 1 | a0001c0001t0004g0080 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.636+406A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757103 | ||||||
chr5:60757280
|
A | T | 9 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0086others(6): Show | 9 | HG01109.hp2 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+229T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757280 | ||||||
chr5:60757354
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.636+155T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757354 | ||||||
chr5:60757366
|
A | G | 1 | a0001c0001t0004g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.636+143T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757366 | ||||||
chr5:60757393
|
C | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(10): Show | 14 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.636+116G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757393 | ||||||
chr5:60757395
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.636+114G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757395 | ||||||
chr5:60757950
|
A | G | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.500-305T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60757950 | ||||||
chr5:60758707
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0227a0001c0001t0002g0235others(1): Show | 5 | HG00621.hp1 NA18945.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-1062C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758707 | ||||||
chr5:60758733
|
C | T | 1 | a0001c0001t0008g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.500-1088G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758733 | ||||||
chr5:60758771
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.500-1126C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758771 | ||||||
chr5:60758799
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.500-1154A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758799 | ||||||
chr5:60759104
|
C | G | 35 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-1459G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759104 | ||||||
chr5:60759293
|
C | T | 1 | a0001c0001t0010g0247 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.500-1648G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759293 | ||||||
chr5:60759409
|
AAATAG | A | 10 | a0001c0001t0002g0054a0001c0001t0002g0103a0001c0001t0002g0207others(7): Show | 10 | HG02135.hp1 NA18939.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-1769_500-1765d others(7): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759409 | ||||||
chr5:60759573
|
C | A | 1 | a0001c0001t0003g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500-1928G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759573 | ||||||
chr5:60759608
|
C | CT | 148 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(145): Show | 152 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.500-1964dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759608 | ||||||
chr5:60759677
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-2032C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759677 | ||||||
chr5:60759784
|
T | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.500-2139A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759784 | ||||||
chr5:60759817
|
T | A | 22 | a0001c0001t0003g0038a0001c0001t0003g0146a0001c0001t0003g0148others(19): Show | 22 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.500-2172A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759817 | ||||||
chr5:60760028
|
C | T | 25 | a0001c0001t0001g0098a0001c0001t0001g0154a0001c0001t0001g0167others(22): Show | 25 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.500-2383G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760028 | ||||||
chr5:60760086
|
C | T | 59 | a0001c0001t0002g0002a0001c0001t0002g0049a0001c0001t0002g0054others(56): Show | 60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.500-2441G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760086 | ||||||
chr5:60760282
|
G | A | 1 | a0001c0001t0004g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.500-2637C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760282 | ||||||
chr5:60760410
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.500-2765A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760410 | ||||||
chr5:60760699
|
C | T | 2 | a0001c0001t0020g0130a0001c0001t0021g0196 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.500-3054G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760699 | ||||||
chr5:60760762
|
C | T | 151 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(148): Show | 155 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.500-3117G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760762 | ||||||
chr5:60761037
|
A | ATGTT | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+3189_499+3190i others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761037 | ||||||
chr5:60761156
|
G | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+3071C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761156 | ||||||
chr5:60761173
|
T | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+3054A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761173 | ||||||
chr5:60761343
|
C | T | 5 | a0001c0001t0002g0207a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 5 | NA18939.hp1 NA18951.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+2884G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761343 | ||||||
chr5:60761460
|
C | T | 250 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.499+2767G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761460 | ||||||
chr5:60761572
|
C | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+2655G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761572 | ||||||
chr5:60761699
|
A | G | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+2528T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761699 | ||||||
chr5:60761725
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.499+2502G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761725 | ||||||
chr5:60761891
|
C | T | 8 | a0001c0001t0007g0001a0001c0001t0007g0030a0001c0001t0007g0031others(5): Show | 9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.499+2336G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761891 | ||||||
chr5:60761956
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.499+2271G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761956 | ||||||
chr5:60761957
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.499+2270C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761957 | ||||||
chr5:60761991
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.499+2236A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761991 | ||||||
chr5:60762009
|
T | C | 35 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.499+2218A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762009 | ||||||
chr5:60762046
|
T | C | 46 | a0001c0001t0003g0006a0001c0001t0003g0038a0001c0001t0003g0050others(43): Show | 47 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.499+2181A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762046 | ||||||
chr5:60762048
|
A | G | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+2179T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762048 | ||||||
chr5:60762105
|
A | G | 50 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(47): Show | 51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.499+2122T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762105 | ||||||
chr5:60762166
|
G | C | 35 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.499+2061C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762166 | ||||||
chr5:60762213
|
C | T | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.499+2014G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762213 | ||||||
chr5:60762231
|
G | A | 2 | a0001c0001t0003g0162a0001c0001t0003g0166 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.499+1996C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762231 | ||||||
chr5:60762255
|
C | T | 6 | a0001c0001t0003g0149a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+1972G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762255 | ||||||
chr5:60762299
|
C | CA | 13 | a0001c0001t0001g0093a0001c0001t0001g0223a0001c0001t0002g0212others(10): Show | 13 | HG01069.hp2 HG01175.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.499+1927dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | ||||||
chr5:60762299
|
CA | C | 12 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0067others(9): Show | 12 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.499+1927delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | ||||||
chr5:60762299
|
CAA | C | 49 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(46): Show | 50 | HG00099.hp2 HG00673.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.499+1926_499+1927d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | ||||||
chr5:60762299
|
CAAA | C | 40 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(37): Show | 42 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.499+1925_499+1927d others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | ||||||
chr5:60762426
|
C | T | 31 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(28): Show | 33 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.499+1801G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762426 | ||||||
chr5:60762429
|
A | G | 2 | a0001c0001t0006g0142a0001c0003t0006g0141 | 2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.499+1798T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762429 | ||||||
chr5:60762463
|
T | C | 2 | a0001c0001t0012g0243a0001c0001t0012g0244 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.499+1764A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762463 | ||||||
chr5:60762571
|
C | T | 50 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(47): Show | 51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.499+1656G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762571 | ||||||
chr5:60762625
|
G | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+1602C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762625 | ||||||
chr5:60763031
|
C | T | 186 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(183): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.499+1196G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60763031 | ||||||
chr5:60763160
|
A | G | 49 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(46): Show | 50 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.499+1067T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60763160 | ||||||
chr5:60763305
|
T | C | 49 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(46): Show | 50 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.499+922A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60763305 | ||||||
chr5:60764181
|
T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+46A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60764181 | ||||||
chr5:60764645
|
T | TA | 59 | a0001c0001t0002g0002a0001c0001t0002g0049a0001c0001t0002g0054others(56): Show | 60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.394-314dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60764645 | ||||||
chr5:60764729
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.394-397A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60764729 | ||||||
chr5:60764870
|
C | T | 28 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(25): Show | 30 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.394-538G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60764870 | ||||||
chr5:60765063
|
G | A | 8 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-731C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765063 | ||||||
chr5:60765135
|
G | C | 8 | a0001c0001t0003g0149a0001c0001t0003g0176a0001c0001t0003g0177others(5): Show | 8 | HG00099.hp2 HG02145.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-803C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765135 | ||||||
chr5:60765190
|
A | C | 2 | a0001c0001t0020g0130a0001c0001t0021g0196 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.394-858T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765190 | ||||||
chr5:60765230
|
G | A | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394-898C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765230 | ||||||
chr5:60765285
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394-953C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765285 | ||||||
chr5:60765329
|
A | G | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-997T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765329 | ||||||
chr5:60765594
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.393+980C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765594 | ||||||
chr5:60765659
|
C | T | 35 | a0001c0001t0001g0098a0001c0001t0001g0154a0001c0001t0001g0167others(32): Show | 36 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.393+915G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765659 | ||||||
chr5:60765727
|
T | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+847A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765727 | ||||||
chr5:60765729
|
G | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0049a0001c0001t0002g0054others(56): Show | 60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.393+845C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765729 | ||||||
chr5:60765976
|
G | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+598C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765976 | ||||||
chr5:60766103
|
C | T | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+471G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766103 | ||||||
chr5:60766266
|
T | C | 2 | a0001c0001t0012g0243a0001c0001t0012g0244 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.393+308A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766266 | ||||||
chr5:60766332
|
G | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+242C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766332 | ||||||
chr5:60766347
|
T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.393+227A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766347 | ||||||
chr5:60766777
|
C | T | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.337-147G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766777 | ||||||
chr5:60766791
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.337-161A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766791 | ||||||
chr5:60766797
|
C | A | 48 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(45): Show | 49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.337-167G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766797 | ||||||
chr5:60766804
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.337-174A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766804 | ||||||
chr5:60766841
|
C | T | 48 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(45): Show | 49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.337-211G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766841 | ||||||
chr5:60766913
|
G | A | 8 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-283C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766913 | ||||||
chr5:60766918
|
T | C | 185 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(182): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.337-288A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766918 | ||||||
chr5:60767067
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.337-437T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767067 | ||||||
chr5:60767185
|
T | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.337-555A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767185 | ||||||
chr5:60767358
|
C | T | 2 | a0001c0001t0013g0007a0001c0001t0022g0174 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.336+465G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767358 | ||||||
chr5:60767369
|
C | A | 9 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0086others(6): Show | 9 | HG01109.hp2 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.336+454G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767369 | ||||||
chr5:60767485
|
C | T | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.336+338G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767485 | ||||||
chr5:60767676
|
T | G | 1 | a0001c0001t0005g0017 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.336+147A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767676 | ||||||
chr5:60767684
|
G | T | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.336+139C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767684 | ||||||
chr5:60767749
|
G | A | 185 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(182): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.336+74C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767749 | ||||||
chr5:60767936
|
A | C | 2 | a0001c0001t0020g0130a0001c0001t0021g0196 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.256-33T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60767936 | ||||||
chr5:60768085
|
T | G | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG03490.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.256-182A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768085 | ||||||
chr5:60768126
|
C | T | 185 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(182): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.256-223G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768126 | ||||||
chr5:60768510
|
G | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.256-607C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768510 | ||||||
chr5:60768558
|
C | T | 48 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(45): Show | 49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.256-655G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768558 | ||||||
chr5:60768784
|
C | T | 2 | a0001c0001t0006g0081a0001c0001t0006g0087 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.256-881G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768784 | ||||||
chr5:60768805
|
CT | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.256-903delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768805 | ||||||
chr5:60769017
|
A | G | 50 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(47): Show | 51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.256-1114T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769017 | ||||||
chr5:60769211
|
G | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.256-1308C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769211 | ||||||
chr5:60769692
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0049a0001c0001t0002g0099others(38): Show | 42 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.256-1789C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769692 | ||||||
chr5:60769778
|
A | G | 1 | a0001c0001t0005g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.256-1875T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769778 | ||||||
chr5:60769855
|
G | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.256-1952C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769855 | ||||||
chr5:60769858
|
T | C | 15 | a0001c0001t0003g0038a0001c0001t0003g0146a0001c0001t0003g0148others(12): Show | 15 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.256-1955A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769858 | ||||||
chr5:60769908
|
A | C | 1 | a0001c0001t0001g0040 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.255+1995T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769908 | ||||||
chr5:60770006
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.255+1897C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770006 | ||||||
chr5:60770029
|
T | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1874A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770029 | ||||||
chr5:60770053
|
G | GA | 61 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(58): Show | 62 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.255+1849dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770053 | ||||||
chr5:60770053
|
GA | G | 90 | a0001c0001t0001g0100a0001c0001t0001g0124a0001c0001t0001g0125others(87): Show | 93 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.255+1849delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770053 | ||||||
chr5:60770114
|
G | T | 48 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(45): Show | 49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.255+1789C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770114 | ||||||
chr5:60770242
|
C | T | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1661G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770242 | ||||||
chr5:60770498
|
C | G | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1405G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770498 | ||||||
chr5:60770669
|
T | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1234A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770669 | ||||||
chr5:60770683
|
A | C | 41 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(38): Show | 43 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.255+1220T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770683 | ||||||
chr5:60770749
|
G | A | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+1154C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770749 | ||||||
chr5:60770839
|
G | A | 35 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.255+1064C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770839 | ||||||
chr5:60771017
|
A | G | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+886T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771017 | ||||||
chr5:60771023
|
C | T | 35 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.255+880G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771023 | ||||||
chr5:60771114
|
C | T | 1 | a0001c0001t0006g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.255+789G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771114 | ||||||
chr5:60771140
|
C | A | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+763G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771140 | ||||||
chr5:60771225
|
A | C | 1 | a0001c0001t0003g0157 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.255+678T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771225 | ||||||
chr5:60771278
|
A | G | 1 | a0001c0001t0001g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.255+625T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771278 | ||||||
chr5:60771357
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.255+546A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771357 | ||||||
chr5:60771723
|
C | T | 35 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.255+180G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771723 | ||||||
chr5:60771877
|
C | T | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.255+26G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771877 | ||||||
chr5:60771891
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.255+12C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771891 | ||||||
chr5:60772520
|
G | A | 50 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0003g0006others(47): Show | 51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.65-427C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60772520 | ||||||
chr5:60772528
|
T | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0049a0001c0001t0002g0099others(54): Show | 58 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.65-435A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60772528 | ||||||
chr5:60772807
|
T | C | 91 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(88): Show | 94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.65-714A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60772807 | ||||||
chr5:60773040
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-947C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773040 | ||||||
chr5:60773230
|
C | T | 88 | a0001c0001t0001g0098a0001c0001t0001g0167a0001c0001t0001g0168others(85): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.65-1137G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773230 | ||||||
chr5:60773327
|
G | A | 1 | a0001c0001t0004g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.65-1234C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773327 | ||||||
chr5:60773340
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65-1247A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773340 | ||||||
chr5:60773510
|
T | C | 1 | a0001c0001t0017g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-1417A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773510 | ||||||
chr5:60773612
|
C | T | 8 | a0001c0001t0007g0001a0001c0001t0007g0030a0001c0001t0007g0031others(5): Show | 9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-1519G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773612 | ||||||
chr5:60774054
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.65-1961A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774054 | ||||||
chr5:60774094
|
A | C | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.65-2001T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774094 | ||||||
chr5:60774107
|
G | A | 147 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(144): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.65-2014C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774107 | ||||||
chr5:60774128
|
A | G | 3 | a0001c0001t0004g0004a0001c0001t0004g0037a0001c0001t0016g0029 | 4 | HG01258.hp1 HG01496.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2035T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774128 | ||||||
chr5:60774228
|
T | A | 8 | a0001c0001t0007g0001a0001c0001t0007g0030a0001c0001t0007g0031others(5): Show | 9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-2135A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774228 | ||||||
chr5:60774275
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.65-2182C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774275 | ||||||
chr5:60774605
|
T | G | 1 | a0001c0001t0004g0077 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.65-2512A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774605 | ||||||
chr5:60774677
|
T | C | 1 | a0001c0001t0002g0239 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.65-2584A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774677 | ||||||
chr5:60774764
|
C | CT | 13 | a0001c0001t0001g0111a0001c0001t0001g0121a0001c0001t0001g0124others(10): Show | 13 | HG01109.hp1 HG01258.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-2672dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774764 | ||||||
chr5:60774764
|
C | CTT | 8 | a0001c0001t0001g0107a0001c0001t0006g0139a0001c0001t0006g0142others(5): Show | 8 | HG01175.hp2 HG03098.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-2673_65-2672dup others(2): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774764 | ||||||
chr5:60774766
|
T | C | 1 | a0001c0001t0005g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.65-2673A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774766 | ||||||
chr5:60775074
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.65-2981A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775074 | ||||||
chr5:60775291
|
T | C | 1 | a0001c0001t0012g0244 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-3198A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775291 | ||||||
chr5:60775452
|
A | AT | 54 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(51): Show | 55 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.65-3360dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775452 | ||||||
chr5:60775682
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.65-3589T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775682 | ||||||
chr5:60775784
|
G | A | 3 | a0001c0001t0010g0246a0001c0001t0010g0247a0001c0001t0010g0248 | 3 | HG00140.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.65-3691C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775784 | ||||||
chr5:60775813
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.65-3720A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775813 | ||||||
chr5:60775954
|
C | G | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.65-3861G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775954 | ||||||
chr5:60776220
|
C | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0189 | 2 | NA18997.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.65-4127G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776220 | ||||||
chr5:60776650
|
A | G | 68 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(65): Show | 69 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-4557T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776650 | ||||||
chr5:60776908
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-4815A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776908 | ||||||
chr5:60776952
|
A | G | 34 | a0001c0001t0001g0098a0001c0001t0001g0140a0001c0001t0001g0168others(31): Show | 35 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.65-4859T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776952 | ||||||
chr5:60777190
|
C | G | 10 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(7): Show | 10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5097G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777190 | ||||||
chr5:60777281
|
AC | A | 10 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(7): Show | 10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5189delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777281 | ||||||
chr5:60777311
|
T | C | 10 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(7): Show | 10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5218A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777311 | ||||||
chr5:60777382
|
TA | T | 7 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-5290delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777382 | ||||||
chr5:60777392
|
A | T | 54 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(51): Show | 55 | HG00673.hp1 HG01109.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.65-5299T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777392 | ||||||
chr5:60777398
|
A | T | 33 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0173others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.65-5305T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777398 | ||||||
chr5:60777492
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.65-5399G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777492 | ||||||
chr5:60778173
|
T | C | 147 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(144): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.65-6080A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778173 | ||||||
chr5:60778348
|
C | G | 1 | a0001c0001t0005g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.65-6255G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778348 | ||||||
chr5:60778368
|
C | G | 3 | a0001c0001t0003g0201a0001c0001t0011g0202a0001c0001t0011g0203 | 3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.65-6275G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778368 | ||||||
chr5:60778391
|
C | T | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.65-6298G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778391 | ||||||
chr5:60778669
|
C | T | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-6576G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778669 | ||||||
chr5:60779260
|
G | T | 10 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(7): Show | 10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-7167C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779260 | ||||||
chr5:60779366
|
C | T | 43 | a0001c0001t0002g0113a0001c0001t0002g0207a0001c0001t0002g0208others(40): Show | 43 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.65-7273G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779366 | ||||||
chr5:60779481
|
A | T | 9 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(6): Show | 9 | HG01175.hp2 HG02735.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-7388T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779481 | ||||||
chr5:60779501
|
C | T | 147 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(144): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.65-7408G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779501 | ||||||
chr5:60779688
|
T | C | 9 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(6): Show | 9 | HG01175.hp2 HG02735.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-7595A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779688 | ||||||
chr5:60780114
|
C | CT | 9 | a0001c0001t0001g0111a0001c0001t0001g0168a0001c0001t0001g0218others(6): Show | 9 | HG00140.hp1 HG00438.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+7219dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780114 | ||||||
chr5:60780114
|
CT | C | 5 | a0001c0001t0001g0097a0001c0001t0002g0216a0001c0001t0006g0165others(2): Show | 5 | HG01257.hp1 HG02572.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7219delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780114 | ||||||
chr5:60780114
|
CTT | C | 62 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(59): Show | 63 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.64+7218_64+7219del others(2): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780114 | ||||||
chr5:60780149
|
C | T | 8 | a0001c0001t0007g0001a0001c0001t0007g0030a0001c0001t0007g0031others(5): Show | 9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+7185G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780149 | ||||||
chr5:60780188
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0199 | 2 | HG01433.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.64+7146G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780188 | ||||||
chr5:60780189
|
G | A | 33 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0173others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+7145C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780189 | ||||||
chr5:60780530
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.64+6804C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780530 | ||||||
chr5:60780531
|
C | T | 1 | a0001c0001t0003g0006 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64+6803G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780531 | ||||||
chr5:60780717
|
G | T | 2 | a0001c0001t0012g0243a0001c0001t0012g0244 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.64+6617C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780717 | ||||||
chr5:60780793
|
C | T | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+6541G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780793 | ||||||
chr5:60781012
|
C | A | 3 | a0001c0001t0002g0206a0001c0001t0003g0171a0001c0001t0008g0205 | 3 | HG01167.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.64+6322G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781012 | ||||||
chr5:60781096
|
G | T | 9 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(6): Show | 9 | HG01175.hp2 HG02735.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+6238C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781096 | ||||||
chr5:60781212
|
G | GA | 36 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0173others(33): Show | 37 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.64+6121dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781212 | ||||||
chr5:60781212
|
GA | G | 12 | a0001c0001t0001g0124a0001c0001t0006g0139a0001c0001t0006g0142others(9): Show | 12 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.64+6121delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781212 | ||||||
chr5:60781385
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.64+5949C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781385 | ||||||
chr5:60781460
|
GA | G | 11 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(8): Show | 11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+5873delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781460 | ||||||
chr5:60781627
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0120 | 3 | HG02896.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.64+5707G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781627 | ||||||
chr5:60782022
|
A | C | 1 | a0001c0001t0005g0017 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.64+5312T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782022 | ||||||
chr5:60782085
|
T | G | 147 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(144): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.64+5249A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782085 | ||||||
chr5:60782585
|
C | T | 147 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(144): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.64+4749G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782585 | ||||||
chr5:60782745
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4589T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782745 | ||||||
chr5:60782746
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4588A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782746 | ||||||
chr5:60782748
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4586T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782748 | ||||||
chr5:60782758
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4576T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782758 | ||||||
chr5:60782766
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64+4568A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782766 | ||||||
chr5:60782879
|
A | G | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+4455T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782879 | ||||||
chr5:60783231
|
T | C | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+4103A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783231 | ||||||
chr5:60783404
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64+3930G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783404 | ||||||
chr5:60783543
|
T | C | 1 | a0001c0001t0008g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+3791A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783543 | ||||||
chr5:60783554
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0122 | 3 | HG00639.hp1 HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.64+3780T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783554 | ||||||
chr5:60783873
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+3461T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783873 | ||||||
chr5:60783995
|
C | A | 10 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(7): Show | 10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+3339G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783995 | ||||||
chr5:60784300
|
C | T | 11 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(8): Show | 11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+3034G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784300 | ||||||
chr5:60784354
|
G | A | 15 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+2980C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784354 | ||||||
chr5:60784512
|
C | T | 1 | a0001c0001t0004g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64+2822G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784512 | ||||||
chr5:60784547
|
A | G | 53 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(50): Show | 54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+2787T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784547 | ||||||
chr5:60784567
|
C | G | 11 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(8): Show | 11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+2767G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784567 | ||||||
chr5:60784591
|
G | T | 53 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(50): Show | 54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+2743C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784591 | ||||||
chr5:60784596
|
C | T | 33 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0173others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+2738G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784596 | ||||||
chr5:60784789
|
G | A | 12 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(9): Show | 12 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.64+2545C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784789 | ||||||
chr5:60785008
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64+2326C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785008 | ||||||
chr5:60785028
|
T | C | 11 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(8): Show | 11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+2306A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785028 | ||||||
chr5:60785052
|
C | T | 3 | a0001c0001t0003g0201a0001c0001t0011g0202a0001c0001t0011g0203 | 3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.64+2282G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785052 | ||||||
chr5:60785198
|
C | T | 33 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0173others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+2136G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785198 | ||||||
chr5:60785469
|
T | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(50): Show | 54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1865A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785469 | ||||||
chr5:60785491
|
T | C | 33 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0173others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+1843A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785491 | ||||||
chr5:60785688
|
G | C | 1 | a0001c0001t0004g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64+1646C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785688 | ||||||
chr5:60785723
|
T | TCATTA | 11 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(8): Show | 11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+1610_64+1611ins others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785723 | ||||||
chr5:60785981
|
T | C | 22 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0037others(19): Show | 24 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.64+1353A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785981 | ||||||
chr5:60786004
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64+1330G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786004 | ||||||
chr5:60786222
|
G | A | 11 | a0001c0001t0006g0139a0001c0001t0006g0142a0001c0001t0006g0143others(8): Show | 11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+1112C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786222 | ||||||
chr5:60786329
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64+1005G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786329 | ||||||
chr5:60786341
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+993A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786341 | ||||||
chr5:60786390
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64+944G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786390 | ||||||
chr5:60786403
|
C | T | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+931G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786403 | ||||||
chr5:60786513
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+821A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786513 | ||||||
chr5:60786718
|
G | A | 61 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0001g0154others(58): Show | 62 | HG00099.hp2 HG00639.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.64+616C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786718 | ||||||
chr5:60786721
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.64+613G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786721 | ||||||
chr5:60786814
|
T | C | 148 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0125others(145): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.64+520A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786814 | ||||||
chr5:60786908
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+426C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786908 | ||||||
chr5:60786923
|
C | A | 1 | a0001c0001t0004g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64+411G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786923 | ||||||
chr5:60786975
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+359C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786975 | ||||||
chr5:60787240
|
A | C | 1 | a0001c0001t0001g0223 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.64+94T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60787240 | ||||||
chr5:60787448
|
C | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-34-17G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60787448 | ||||||
chr5:60787472
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-41T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60787472 | ||||||
chr5:60787675
|
A | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0093others(5): Show | 8 | NA18959.hp1 NA18967.hp1 NA18997.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-244T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60787675 | ||||||
chr5:60788076
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-34-645T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788076 | ||||||
chr5:60788193
|
T | C | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-762A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788193 | ||||||
chr5:60788291
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-860A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788291 | ||||||
chr5:60788328
|
T | C | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-897A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788328 | ||||||
chr5:60788496
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-34-1065G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788496 | ||||||
chr5:60788522
|
C | T | 1 | a0001c0001t0007g0028 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-34-1091G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788522 | ||||||
chr5:60788589
|
A | G | 1 | a0001c0001t0004g0080 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-34-1158T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788589 | ||||||
chr5:60788664
|
AC | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-34-1234delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788664 | ||||||
chr5:60788667
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0054 | 2 | NA18970.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-34-1236G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788667 | ||||||
chr5:60788881
|
G | A | 1 | a0001c0001t0023g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-34-1450C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788881 | ||||||
chr5:60788945
|
T | C | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-1514A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788945 | ||||||
chr5:60789066
|
A | G | 1 | a0001c0001t0010g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-34-1635T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789066 | ||||||
chr5:60789284
|
A | C | 2 | a0001c0001t0002g0233a0001c0001t0002g0238 | 2 | HG02523.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-34-1853T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789284 | ||||||
chr5:60789413
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-34-1982C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789413 | ||||||
chr5:60789427
|
A | T | 1 | a0001c0001t0006g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-34-1996T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789427 | ||||||
chr5:60789662
|
A | G | 4 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(1): Show | 4 | HG01099.hp2 HG01168.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-2231T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789662 | ||||||
chr5:60789802
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-34-2371T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789802 | ||||||
chr5:60789843
|
G | C | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-2412C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789843 | ||||||
chr5:60789909
|
G | A | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-34-2478C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789909 | ||||||
chr5:60789936
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-34-2505C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789936 | ||||||
chr5:60790055
|
T | C | 7 | a0001c0001t0001g0173a0001c0001t0003g0150a0001c0001t0003g0155others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-2624A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790055 | ||||||
chr5:60790104
|
T | C | 2 | a0001c0001t0001g0088a0003c0004t0001g0085 | 2 | NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-34-2673A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790104 | ||||||
chr5:60790235
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-34-2804A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790235 | ||||||
chr5:60790248
|
G | T | 1 | a0001c0001t0005g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-34-2817C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790248 | ||||||
chr5:60790554
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-34-3123G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790554 | ||||||
chr5:60790571
|
T | G | 1 | a0001c0001t0002g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-34-3140A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790571 | ||||||
chr5:60790633
|
T | C | 20 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0173others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34-3202A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790633 | ||||||
chr5:60790850
|
T | G | 22 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-3419A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790850 | ||||||
chr5:60790909
|
A | T | 1 | a0001c0001t0003g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-34-3478T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790909 | ||||||
chr5:60790923
|
A | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-3492T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790923 | ||||||
chr5:60790940
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-3509C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790940 | ||||||
chr5:60790983
|
G | T | 6 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(3): Show | 6 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-3552C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790983 | ||||||
chr5:60791073
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(88): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-34-3642G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791073 | ||||||
chr5:60791509
|
G | A | 15 | a0001c0001t0002g0183a0001c0001t0002g0185a0001c0001t0002g0186others(12): Show | 15 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34-4078C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791509 | ||||||
chr5:60791550
|
C | A | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-4119G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791550 | ||||||
chr5:60791700
|
T | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-4269A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791700 | ||||||
chr5:60791955
|
C | A | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-34-4524G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791955 | ||||||
chr5:60792123
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-4692C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792123 | ||||||
chr5:60792153
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-4722C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792153 | ||||||
chr5:60792321
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-34-4890T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792321 | ||||||
chr5:60792355
|
T | G | 1 | a0001c0001t0003g0149 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-34-4924A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792355 | ||||||
chr5:60792423
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-34-4992G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792423 | ||||||
chr5:60792428
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-34-4997A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792428 | ||||||
chr5:60792792
|
C | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-34-5361G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792792 | ||||||
chr5:60792967
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-34-5536T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792967 | ||||||
chr5:60793265
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-34-5834G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793265 | ||||||
chr5:60793310
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+5870C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793310 | ||||||
chr5:60793321
|
C | T | 8 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0086others(5): Show | 8 | HG01109.hp2 HG01261.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+5859G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793321 | ||||||
chr5:60793442
|
G | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+5738C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793442 | ||||||
chr5:60793609
|
T | G | 53 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0173others(50): Show | 54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-35+5571A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793609 | ||||||
chr5:60793640
|
A | C | 3 | a0001c0001t0003g0201a0001c0001t0011g0202a0001c0001t0011g0203 | 3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-35+5540T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793640 | ||||||
chr5:60793907
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-35+5273G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793907 | ||||||
chr5:60793952
|
G | A | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+5228C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793952 | ||||||
chr5:60794056
|
G | A | 6 | a0001c0001t0003g0149a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+5124C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794056 | ||||||
chr5:60794140
|
A | C | 6 | a0001c0001t0001g0140a0001c0001t0006g0139a0001c0001t0006g0142others(3): Show | 6 | HG02809.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+5040T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794140 | ||||||
chr5:60794143
|
T | G | 1 | a0001c0001t0002g0241 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35+5037A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794143 | ||||||
chr5:60794183
|
T | A | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-35+4997A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794183 | ||||||
chr5:60794224
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-35+4956A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794224 | ||||||
chr5:60794524
|
A | T | 2 | a0001c0001t0003g0172a0001c0001t0003g0175 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-35+4656T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794524 | ||||||
chr5:60794655
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-35+4525C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794655 | ||||||
chr5:60794662
|
T | C | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-35+4518A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794662 | ||||||
chr5:60794674
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-35+4506A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794674 | ||||||
chr5:60794975
|
C | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-35+4205G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794975 | ||||||
chr5:60794992
|
G | C | 1 | a0001c0001t0002g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-35+4188C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794992 | ||||||
chr5:60795124
|
C | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+4056G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795124 | ||||||
chr5:60795219
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+3961G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795219 | ||||||
chr5:60795293
|
G | C | 1 | a0001c0001t0003g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-35+3887C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795293 | ||||||
chr5:60795325
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0129 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-35+3855C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795325 | ||||||
chr5:60795365
|
C | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+3815G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795365 | ||||||
chr5:60795459
|
G | A | 1 | a0001c0001t0004g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-35+3721C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795459 | ||||||
chr5:60795478
|
G | C | 2 | a0001c0001t0007g0001a0001c0001t0007g0033 | 3 | HG03490.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-35+3702C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795478 | ||||||
chr5:60795496
|
G | A | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-35+3684C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795496 | ||||||
chr5:60795503
|
T | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+3677A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795503 | ||||||
chr5:60795609
|
G | C | 1 | a0001c0001t0007g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-35+3571C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795609 | ||||||
chr5:60795655
|
T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-35+3525A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795655 | ||||||
chr5:60795729
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+3451T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795729 | ||||||
chr5:60795828
|
G | A | 1 | a0001c0001t0004g0080 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-35+3352C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795828 | ||||||
chr5:60795846
|
AAG | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+3332_-35+3333d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795846 | ||||||
chr5:60795853
|
G | C | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-35+3327C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795853 | ||||||
chr5:60795933
|
T | TGCCGCCA others(15): Show |
1 | a0001c0001t0002g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35+3225_-35+3246d others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795933 | ||||||
chr5:60795975
|
TAAGAACA | T | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+3198_-35+3204d others(9): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795975 | ||||||
chr5:60795991
|
T | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+3189A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795991 | ||||||
chr5:60795995
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35+3185G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795995 | ||||||
chr5:60796009
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-35+3171A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796009 | ||||||
chr5:60796081
|
G | A | 2 | a0001c0001t0006g0081a0001c0001t0006g0087 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-35+3099C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796081 | ||||||
chr5:60796226
|
C | T | 1 | a0001c0001t0003g0192 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-35+2954G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796226 | ||||||
chr5:60796490
|
C | T | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+2690G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796490 | ||||||
chr5:60796504
|
C | G | 6 | a0001c0001t0003g0149a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+2676G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796504 | ||||||
chr5:60796611
|
A | G | 1 | a0001c0001t0004g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-35+2569T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796611 | ||||||
chr5:60796623
|
C | T | 1 | a0001c0001t0003g0006 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-35+2557G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796623 | ||||||
chr5:60796859
|
G | T | 6 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+2321C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796859 | ||||||
chr5:60796860
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+2320C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796860 | ||||||
chr5:60797190
|
G | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0092others(9): Show | 13 | HG00280.hp1 HG00544.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-35+1990C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797190 | ||||||
chr5:60797268
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-35+1912A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797268 | ||||||
chr5:60797275
|
G | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0236 | 2 | HG00735.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-35+1905C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797275 | ||||||
chr5:60797560
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+1620G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797560 | ||||||
chr5:60797785
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-35+1395T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797785 | ||||||
chr5:60797939
|
C | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+1241G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797939 | ||||||
chr5:60798063
|
T | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+1117A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798063 | ||||||
chr5:60798251
|
G | A | 2 | a0001c0001t0003g0114a0001c0001t0004g0053 | 2 | HG02486.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-35+929C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798251 | ||||||
chr5:60798313
|
T | C | 17 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0173others(14): Show | 17 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+867A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798313 | ||||||
chr5:60798345
|
C | T | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+835G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798345 | ||||||
chr5:60798350
|
T | G | 1 | a0001c0001t0004g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-35+830A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798350 | ||||||
chr5:60798412
|
C | T | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+768G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798412 | ||||||
chr5:60798439
|
G | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-35+741C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798439 | ||||||
chr5:60798519
|
G | A | 2 | a0001c0001t0004g0046a0001c0001t0004g0074 | 2 | HG02056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-35+661C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798519 | ||||||
chr5:60799177
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(53): Show | 57 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.-35+3A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60799177 | ||||||
chr5:60799248
|
A | T | 8 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0086others(5): Show | 8 | HG01109.hp2 HG01261.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85-18T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799248 | ||||||
chr5:60799428
|
C | T | 1 | a0001c0001t0008g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-85-198G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799428 | ||||||
chr5:60799445
|
G | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(150): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-215C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799445 | ||||||
chr5:60799502
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-85-272T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799502 | ||||||
chr5:60799514
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-85-284C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799514 | ||||||
chr5:60799546
|
A | T | 4 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0153others(1): Show | 4 | HG02630.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-316T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799546 | ||||||
chr5:60799553
|
A | G | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-323T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799553 | ||||||
chr5:60799557
|
C | T | 9 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0012others(6): Show | 9 | HG00140.hp1 HG00738.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-327G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799557 | ||||||
chr5:60799734
|
A | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0222 | 2 | NA18983.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-85-504T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799734 | ||||||
chr5:60799781
|
T | C | 13 | a0001c0001t0001g0048a0001c0001t0001g0078a0001c0001t0001g0079others(10): Show | 13 | HG00438.hp2 HG02027.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.-85-551A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799781 | ||||||
chr5:60799841
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-85-611A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799841 | ||||||
chr5:60799899
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-85-669A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799899 | ||||||
chr5:60799900
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-85-670C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799900 | ||||||
chr5:60799908
|
A | G | 6 | a0001c0001t0001g0140a0001c0001t0006g0139a0001c0001t0006g0142others(3): Show | 6 | HG02809.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-678T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799908 | ||||||
chr5:60799969
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-739C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799969 | ||||||
chr5:60799993
|
C | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0077a0001c0001t0004g0090 | 4 | NA18612.hp1 NA18945.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-763G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799993 | ||||||
chr5:60800030
|
C | CA | 23 | a0001c0001t0001g0168a0001c0001t0002g0208a0001c0001t0002g0212others(20): Show | 23 | HG00140.hp1 HG00738.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.-85-801dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | ||||||
chr5:60800030
|
CA | C | 6 | a0001c0001t0002g0240a0001c0001t0007g0032a0001c0001t0008g0132others(3): Show | 6 | HG01496.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-801delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | ||||||
chr5:60800030
|
CAAAAAA | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(141): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-85-806_-85-801del others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | ||||||
chr5:60800030
|
CAAAAAAA | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0151a0001c0001t0002g0206others(4): Show | 7 | HG01884.hp1 HG02132.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-807_-85-801del others(7): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | ||||||
chr5:60800030
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-85-813_-85-801del others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | ||||||
chr5:60800056
|
T | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-85-826A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800056 | ||||||
chr5:60800206
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-976A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800206 | ||||||
chr5:60800400
|
G | A | 3 | a0001c0001t0002g0206a0001c0001t0003g0171a0001c0001t0008g0205 | 3 | HG01167.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-85-1170C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800400 | ||||||
chr5:60800456
|
A | C | 2 | a0001c0001t0002g0207a0001c0001t0002g0211 | 2 | NA18939.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-85-1226T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800456 | ||||||
chr5:60800670
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-85-1440A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800670 | ||||||
chr5:60800722
|
G | A | 2 | a0001c0001t0012g0243a0001c0001t0012g0244 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-85-1492C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800722 | ||||||
chr5:60800778
|
TC | T | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-1549delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800778 | ||||||
chr5:60800825
|
T | G | 2 | a0001c0001t0007g0001a0001c0001t0007g0033 | 3 | HG03490.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-85-1595A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800825 | ||||||
chr5:60801324
|
C | CA | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2095dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801324 | ||||||
chr5:60801333
|
A | T | 5 | a0001c0001t0002g0207a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 5 | NA18939.hp1 NA18951.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-2103T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801333 | ||||||
chr5:60801444
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-85-2214C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801444 | ||||||
chr5:60801506
|
A | AG | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2277dupC | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801506 | ||||||
chr5:60801584
|
A | T | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2354T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801584 | ||||||
chr5:60801726
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-85-2496C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801726 | ||||||
chr5:60801731
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-85-2501A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801731 | ||||||
chr5:60801877
|
A | T | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2647T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801877 | ||||||
chr5:60801971
|
G | C | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-2741C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801971 | ||||||
chr5:60802061
|
C | CAT | 5 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0005g0008others(2): Show | 5 | HG00621.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-2833_-85-2832d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
C | CATATATA others(3): Show |
1 | a0001c0001t0005g0010 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-85-2841_-85-2832d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CAT | C | 5 | a0001c0001t0001g0140a0001c0001t0002g0231a0001c0001t0002g0234others(2): Show | 5 | HG00738.hp2 HG02602.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-2833_-85-2832d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATAT | C | 6 | a0001c0001t0002g0235a0001c0001t0006g0142a0001c0001t0006g0143others(3): Show | 6 | HG00140.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2835_-85-2832d others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATATAT | C | 3 | a0001c0001t0006g0139a0001c0001t0008g0137a0001c0001t0009g0245 | 3 | HG01981.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-85-2837_-85-2832d others(8): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATATATA others(3): Show |
C | 5 | a0001c0001t0002g0220a0001c0001t0002g0222a0001c0001t0002g0227others(2): Show | 5 | NA18906.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-2841_-85-2832d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATATATA others(5): Show |
C | 7 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216others(4): Show | 7 | HG01099.hp1 HG03490.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-2843_-85-2832d others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATATATA others(7): Show |
C | 5 | a0001c0001t0002g0230a0001c0001t0002g0239a0001c0001t0002g0240others(2): Show | 5 | HG00639.hp2 HG01261.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-2845_-85-2832d others(16): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0002g0208a0001c0001t0002g0213 | 2 | HG03831.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-85-2847_-85-2832d others(18): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802061
|
CATATATA others(11): Show |
C | 6 | a0001c0001t0002g0207a0001c0001t0002g0209a0001c0001t0002g0210others(3): Show | 6 | HG02135.hp1 NA18939.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2849_-85-2832d others(20): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | ||||||
chr5:60802073
|
TATATATA others(41): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-2891_-85-2844d others(50): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802073 | ||||||
chr5:60802081
|
TATATATA others(37): Show |
T | 48 | a0001c0001t0001g0040a0001c0001t0001g0131a0001c0001t0001g0151others(45): Show | 49 | HG00099.hp2 HG00673.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2852d others(46): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802081 | ||||||
chr5:60802083
|
TATATATA others(33): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-85-2893_-85-2854d others(42): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802083 | ||||||
chr5:60802083
|
TATATATA others(35): Show |
T | 96 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0045others(93): Show | 100 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2854d others(44): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802083 | ||||||
chr5:60802085
|
TATATATA others(33): Show |
T | 4 | a0001c0001t0001g0107a0001c0001t0004g0074a0001c0001t0006g0081others(1): Show | 4 | HG02056.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2856d others(42): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802085 | ||||||
chr5:60802087
|
TATATATA others(31): Show |
T | 10 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0122others(7): Show | 10 | HG00639.hp1 HG01167.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2858d others(40): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802087 | ||||||
chr5:60802089
|
TATATATA others(23): Show |
T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2889_-85-2860d others(32): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802089 | ||||||
chr5:60802089
|
TATATATA others(29): Show |
T | 1 | a0001c0001t0001g0218 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-85-2895_-85-2860d others(38): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802089 | ||||||
chr5:60802091
|
TATATATA others(27): Show |
T | 1 | a0001c0001t0006g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-85-2895_-85-2862d others(36): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802091 | ||||||
chr5:60802099
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0016g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-2889_-85-2870d others(22): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802099 | ||||||
chr5:60802101
|
TATATATA others(11): Show |
T | 5 | a0001c0001t0005g0014a0001c0001t0007g0001a0001c0001t0007g0031others(2): Show | 6 | HG00280.hp2 HG01496.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2889_-85-2872d others(20): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802101 | ||||||
chr5:60802103
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0007g0033 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-85-2889_-85-2874d others(18): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802103 | ||||||
chr5:60802105
|
TATATATA others(7): Show |
T | 6 | a0001c0001t0002g0233a0001c0001t0002g0238a0001c0001t0005g0017others(3): Show | 6 | HG01192.hp2 HG01952.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2889_-85-2876d others(16): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802105 | ||||||
chr5:60802107
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0007g0030 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-85-2889_-85-2878d others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802107 | ||||||
chr5:60802109
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0005g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-85-2889_-85-2880d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802109 | ||||||
chr5:60802113
|
T | C | 1 | a0001c0001t0008g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-2883A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802113 | ||||||
chr5:60802115
|
T | C | 4 | a0001c0001t0002g0207a0001c0001t0002g0211a0001c0001t0008g0134others(1): Show | 4 | HG02622.hp1 NA18939.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2885A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802115 | ||||||
chr5:60802115
|
TATAC | T | 3 | a0001c0001t0005g0011a0001c0001t0005g0015a0001c0001t0005g0022 | 3 | HG01069.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-85-2889_-85-2886d others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802115 | ||||||
chr5:60802117
|
T | C | 20 | a0001c0001t0001g0140a0001c0001t0002g0207a0001c0001t0002g0208others(17): Show | 20 | HG02135.hp1 HG02622.hp1 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.-85-2887A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802117 | ||||||
chr5:60802117
|
TAC | T | 3 | a0001c0001t0005g0012a0001c0001t0005g0021a0001c0001t0015g0020 | 3 | HG00738.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-85-2889_-85-2888d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802117 | ||||||
chr5:60802119
|
C | T | 11 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(8): Show | 11 | HG00140.hp1 HG01099.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-2889G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802119 | ||||||
chr5:60802123
|
C | T | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-2893G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802123 | ||||||
chr5:60802257
|
T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-85-3027A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802257 | ||||||
chr5:60802419
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-85-3189A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802419 | ||||||
chr5:60802440
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(158): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-85-3210T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802440 | ||||||
chr5:60802748
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-85-3518T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802748 | ||||||
chr5:60802962
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-3732G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802962 | ||||||
chr5:60803034
|
C | T | 13 | a0001c0001t0001g0140a0001c0001t0006g0139a0001c0001t0006g0142others(10): Show | 13 | HG02622.hp1 HG02647.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-3804G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803034 | ||||||
chr5:60803467
|
C | T | 1 | a0001c0001t0004g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-85-4237G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803467 | ||||||
chr5:60803468
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-85-4238C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803468 | ||||||
chr5:60803631
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0008g0205 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-85-4401C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803631 | ||||||
chr5:60803904
|
A | T | 2 | a0001c0001t0005g0013a0001c0001t0005g0014 | 2 | NA20300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-85-4674T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803904 | ||||||
chr5:60803976
|
T | C | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-4746A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803976 | ||||||
chr5:60804083
|
T | C | 2 | a0001c0001t0002g0235a0001c0001t0002g0237 | 2 | HG00621.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-85-4853A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60804083 | ||||||
chr5:60804562
|
A | G | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-5332T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60804562 | ||||||
chr5:60804617
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-85-5387G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60804617 | ||||||
chr5:60805036
|
A | G | 2 | a0001c0001t0003g0184a0001c0001t0003g0192 | 2 | HG00673.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-85-5806T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805036 | ||||||
chr5:60805110
|
C | T | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-85-5880G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805110 | ||||||
chr5:60805282
|
C | A | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-85-6052G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805282 | ||||||
chr5:60805426
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-6196C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805426 | ||||||
chr5:60805465
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-85-6235T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805465 | ||||||
chr5:60805470
|
G | A | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-6240C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805470 | ||||||
chr5:60805490
|
T | C | 1 | a0001c0001t0002g0241 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-85-6260A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805490 | ||||||
chr5:60805862
|
T | C | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-6632A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805862 | ||||||
chr5:60806488
|
C | G | 2 | a0001c0001t0003g0195a0001c0001t0003g0197 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-85-7258G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806488 | ||||||
chr5:60806607
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-85-7377A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806607 | ||||||
chr5:60806717
|
C | T | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-7487G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806717 | ||||||
chr5:60806903
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-7673T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806903 | ||||||
chr5:60806994
|
G | A | 1 | a0001c0001t0005g0010 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-85-7764C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806994 | ||||||
chr5:60807095
|
A | G | 2 | a0001c0001t0004g0071a0001c0001t0004g0072 | 2 | HG02523.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-85-7865T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807095 | ||||||
chr5:60807107
|
G | T | 7 | a0001c0001t0001g0131a0001c0001t0006g0145a0001c0001t0006g0165others(4): Show | 7 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-7877C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807107 | ||||||
chr5:60807266
|
A | T | 2 | a0001c0001t0004g0071a0001c0001t0004g0072 | 2 | HG02523.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-85-8036T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807266 | ||||||
chr5:60807530
|
G | GA | 192 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(189): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-85-8301dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807530 | ||||||
chr5:60807625
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-8395G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807625 | ||||||
chr5:60807665
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-85-8435T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807665 | ||||||
chr5:60807726
|
G | A | 2 | a0001c0001t0009g0245a0001c0001t0009g0252 | 2 | HG01981.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-85-8496C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807726 | ||||||
chr5:60807727
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-8497G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807727 | ||||||
chr5:60807737
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-8507G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807737 | ||||||
chr5:60807770
|
C | A | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-85-8540G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807770 | ||||||
chr5:60807771
|
A | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-85-8541T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807771 | ||||||
chr5:60807826
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-85-8596G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807826 | ||||||
chr5:60807827
|
G | A | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-8597C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807827 | ||||||
chr5:60807843
|
CA | C | 22 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216others(19): Show | 22 | HG00621.hp1 HG00639.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-85-8614delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807843 | ||||||
chr5:60807988
|
G | A | 1 | a0001c0001t0004g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-85-8758C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807988 | ||||||
chr5:60807992
|
C | A | 1 | a0001c0001t0004g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-85-8762G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | ||||||
chr5:60807992
|
C | CA | 41 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0167others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.-85-8763dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | ||||||
chr5:60807992
|
C | CAA | 12 | a0001c0001t0002g0214a0001c0001t0002g0216a0001c0001t0002g0220others(9): Show | 12 | HG00621.hp1 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-8764_-85-8763d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | ||||||
chr5:60807992
|
CA | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(118): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-85-8763delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | ||||||
chr5:60807992
|
CAA | C | 9 | a0001c0001t0001g0084a0001c0001t0001g0100a0001c0001t0001g0107others(6): Show | 9 | HG01168.hp2 HG01175.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-8764_-85-8763d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | ||||||
chr5:60807992
|
CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-8778_-85-8763d others(18): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | ||||||
chr5:60808330
|
T | C | 7 | a0001c0001t0001g0131a0001c0001t0006g0145a0001c0001t0006g0165others(4): Show | 7 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-9100A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808330 | ||||||
chr5:60808408
|
A | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-9178T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808408 | ||||||
chr5:60808533
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-9303A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808533 | ||||||
chr5:60808675
|
G | GT | 4 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(1): Show | 4 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-9446dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808675 | ||||||
chr5:60808763
|
A | G | 1 | a0001c0001t0005g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-85-9533T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808763 | ||||||
chr5:60809275
|
A | T | 1 | a0001c0001t0004g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-85-10045T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809275 | ||||||
chr5:60809409
|
T | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-10179A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809409 | ||||||
chr5:60809673
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0122 | 2 | HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-85-10443C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809673 | ||||||
chr5:60809708
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-10478G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809708 | ||||||
chr5:60809798
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-85-10568C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809798 | ||||||
chr5:60809800
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-85-10570G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809800 | ||||||
chr5:60810179
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-10949C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810179 | ||||||
chr5:60810237
|
T | C | 3 | a0001c0001t0003g0201a0001c0001t0011g0202a0001c0001t0011g0203 | 3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-85-11007A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810237 | ||||||
chr5:60810420
|
C | T | 2 | a0001c0001t0003g0162a0001c0001t0003g0166 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-85-11190G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810420 | ||||||
chr5:60810656
|
G | A | 1 | a0001c0001t0012g0244 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-85-11426C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810656 | ||||||
chr5:60810736
|
T | G | 1 | a0001c0001t0003g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-85-11506A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810736 | ||||||
chr5:60810784
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-85-11554C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810784 | ||||||
chr5:60811175
|
TA | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-11946delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811175 | ||||||
chr5:60811182
|
A | C | 1 | a0001c0001t0005g0009 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-85-11952T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811182 | ||||||
chr5:60811236
|
G | C | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-85-12006C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811236 | ||||||
chr5:60811283
|
T | G | 1 | a0001c0001t0002g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-85-12053A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811283 | ||||||
chr5:60811463
|
A | G | 1 | a0001c0001t0006g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-85-12233T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811463 | ||||||
chr5:60811858
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-85-12628T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811858 | ||||||
chr5:60812230
|
T | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-13000A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812230 | ||||||
chr5:60812338
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-13108T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812338 | ||||||
chr5:60812388
|
T | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0088a0001c0001t0001g0106others(4): Show | 7 | HG00408.hp1 NA18970.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-13158A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812388 | ||||||
chr5:60812443
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0121 | 3 | NA19004.hp1 NA19074.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-85-13213C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812443 | ||||||
chr5:60812643
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-85-13413A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812643 | ||||||
chr5:60812703
|
T | C | 3 | a0001c0001t0006g0165a0001c0001t0006g0204a0001c0001t0023g0164 | 3 | HG01175.hp2 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-85-13473A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812703 | ||||||
chr5:60812724
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-13494C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812724 | ||||||
chr5:60812844
|
G | C | 55 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0173others(52): Show | 56 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.-85-13614C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812844 | ||||||
chr5:60812884
|
G | A | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-13654C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812884 | ||||||
chr5:60812923
|
T | G | 1 | a0001c0003t0006g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-85-13693A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812923 | ||||||
chr5:60813097
|
C | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-13867G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813097 | ||||||
chr5:60813134
|
A | G | 22 | a0001c0001t0001g0098a0001c0001t0004g0004a0001c0001t0004g0005others(19): Show | 24 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-85-13904T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813134 | ||||||
chr5:60813230
|
T | C | 1 | a0001c0001t0006g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-85-14000A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813230 | ||||||
chr5:60813324
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-85-14094G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813324 | ||||||
chr5:60813620
|
C | G | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-14390G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813620 | ||||||
chr5:60813695
|
T | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-14465A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813695 | ||||||
chr5:60813775
|
A | T | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-85-14545T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813775 | ||||||
chr5:60813780
|
G | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-85-14550C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813780 | ||||||
chr5:60814057
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-14827G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814057 | ||||||
chr5:60814378
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-85-15148A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814378 | ||||||
chr5:60814382
|
A | G | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-15152T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814382 | ||||||
chr5:60814649
|
A | C | 2 | a0001c0001t0001g0131a0001c0001t0020g0130 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-15419T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814649 | ||||||
chr5:60814782
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-85-15552C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814782 | ||||||
chr5:60814785
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-85-15555C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814785 | ||||||
chr5:60815014
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-85-15784T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815014 | ||||||
chr5:60815477
|
C | G | 1 | a0001c0001t0006g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-85-16247G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815477 | ||||||
chr5:60815535
|
C | CAATAAAA others(19): Show |
1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-16331_-85-1630 others(30): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815535 | ||||||
chr5:60815535
|
CAATAAAA others(19): Show |
C | 185 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-16331_-85-1630 others(30): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815535 | ||||||
chr5:60815551
|
TTTTATAA others(18): Show |
T | 1 | a0001c0001t0012g0244 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-85-16346_-85-1632 others(29): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815551 | ||||||
chr5:60815661
|
G | A | 1 | a0001c0001t0023g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-85-16431C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815661 | ||||||
chr5:60815716
|
C | T | 2 | a0001c0001t0006g0081a0001c0001t0006g0087 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-85-16486G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815716 | ||||||
chr5:60815752
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(54): Show | 58 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-85-16522T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815752 | ||||||
chr5:60815826
|
T | C | 1 | a0001c0001t0003g0153 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-85-16596A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815826 | ||||||
chr5:60815983
|
T | C | 1 | a0001c0001t0003g0184 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-85-16753A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815983 | ||||||
chr5:60816083
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-16853T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816083 | ||||||
chr5:60816088
|
T | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0169a0001c0001t0003g0176others(1): Show | 5 | HG00099.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-16858A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816088 | ||||||
chr5:60816122
|
A | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-85-16892T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816122 | ||||||
chr5:60816176
|
T | C | 1 | a0001c0001t0006g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-85-16946A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816176 | ||||||
chr5:60816209
|
A | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(190): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-85-16979T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816209 | ||||||
chr5:60816380
|
C | CA | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-17151dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816380 | ||||||
chr5:60816380
|
CA | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-17151delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816380 | ||||||
chr5:60816610
|
T | C | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-17380A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816610 | ||||||
chr5:60816652
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-85-17422C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816652 | ||||||
chr5:60817679
|
C | CACACACA others(10): Show |
99 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(96): Show | 103 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.-85-18466_-85-1845 others(21): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817679 | ||||||
chr5:60817679
|
CACACACA others(10): Show |
C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-18466_-85-1845 others(21): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817679 | ||||||
chr5:60817810
|
A | G | 3 | a0001c0001t0004g0005a0001c0001t0004g0077a0001c0001t0004g0090 | 4 | NA18612.hp1 NA18945.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-18580T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817810 | ||||||
chr5:60817822
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(186): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.-85-18592C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817822 | ||||||
chr5:60817824
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-18594T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817824 | ||||||
chr5:60817830
|
A | ATG | 6 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0189others(3): Show | 7 | HG02056.hp2 HG02630.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-18602_-85-1860 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817830 | ||||||
chr5:60817842
|
GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-18620_-85-1861 others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817842 | ||||||
chr5:60817848
|
GTA | G | 10 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 10 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-18620_-85-1861 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817848 | ||||||
chr5:60817850
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-18620T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817850 | ||||||
chr5:60817852
|
A | G | 20 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(17): Show | 21 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-85-18622T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817852 | ||||||
chr5:60818319
|
G | GA | 25 | a0001c0001t0001g0094a0001c0001t0001g0140a0001c0001t0001g0167others(22): Show | 25 | HG00438.hp2 HG01175.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-85-19090dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818319 | ||||||
chr5:60818319
|
GA | G | 79 | a0001c0001t0001g0040a0001c0001t0001g0062a0001c0001t0001g0063others(76): Show | 80 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-85-19090delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818319 | ||||||
chr5:60818319
|
GAA | G | 41 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(38): Show | 42 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-85-19091_-85-1909 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818319 | ||||||
chr5:60818408
|
T | C | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-85-19178A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818408 | ||||||
chr5:60818433
|
A | T | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-19203T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818433 | ||||||
chr5:60819015
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-19785T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819015 | ||||||
chr5:60819020
|
A | AGAGGGGA others(8): Show |
3 | a0001c0001t0010g0246a0001c0001t0010g0247a0001c0001t0010g0248 | 3 | HG00140.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-85-19805_-85-1979 others(19): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | ||||||
chr5:60819020
|
A | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0020g0130 | 3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-19790T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | ||||||
chr5:60819020
|
AGAGGG | A | 6 | a0001c0001t0002g0231a0001c0001t0002g0237a0001c0001t0006g0143others(3): Show | 6 | HG00621.hp1 HG01261.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-19795_-85-1979 others(9): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | ||||||
chr5:60819020
|
AGAGGGGA others(3): Show |
A | 14 | a0001c0001t0001g0140a0001c0001t0002g0208a0001c0001t0002g0209others(11): Show | 14 | HG02135.hp1 HG02809.hp1 HG03225.hp1 others(11): Show |
intron_variant | MODIFIER | c.-85-19800_-85-1979 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | ||||||
chr5:60819020
|
AGAGGGGA others(8): Show |
A | 2 | a0001c0001t0002g0207a0001c0001t0002g0213 | 2 | HG03831.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-85-19805_-85-1979 others(19): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | ||||||
chr5:60819020
|
AGAGGGGA others(13): Show |
A | 1 | a0001c0001t0009g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-85-19810_-85-1979 others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | ||||||
chr5:60819023
|
G | C | 1 | a0001c0001t0002g0002 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-85-19793C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819023 | ||||||
chr5:60819031
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19801C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819031 | ||||||
chr5:60819032
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19802T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819032 | ||||||
chr5:60819044
|
GGGAGGGG others(83): Show |
G | 1 | a0001c0001t0019g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-85-19904_-85-1981 others(94): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819044 | ||||||
chr5:60819054
|
GGGAGGGG others(63): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-85-19894_-85-1982 others(74): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819054 | ||||||
chr5:60819055
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-85-19825C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819055 | ||||||
chr5:60819059
|
GGGAGGGG others(38): Show |
G | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-19874_-85-1983 others(49): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | ||||||
chr5:60819059
|
GGGAGGGG others(48): Show |
G | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-19884_-85-1983 others(59): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | ||||||
chr5:60819059
|
GGGAGGGG others(58): Show |
G | 5 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-19894_-85-1983 others(69): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | ||||||
chr5:60819059
|
GGGAGGGG others(68): Show |
G | 2 | a0001c0001t0003g0086a0001c0001t0006g0087 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-85-19904_-85-1983 others(79): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | ||||||
chr5:60819064
|
GGGAGGGG others(43): Show |
G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-19884_-85-1983 others(54): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819064 | ||||||
chr5:60819064
|
GGGAGGGG others(63): Show |
G | 23 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0094others(20): Show | 23 | HG00099.hp1 HG01358.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1983 others(74): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819064 | ||||||
chr5:60819069
|
GGGAGGGG others(28): Show |
G | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-19874_-85-1984 others(39): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819069 | ||||||
chr5:60819069
|
GGGAGGGG others(38): Show |
G | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-85-19884_-85-1984 others(49): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819069 | ||||||
chr5:60819069
|
GGGAGGGG others(58): Show |
G | 43 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(40): Show | 46 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1984 others(69): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819069 | ||||||
chr5:60819070
|
GGAGGGGA others(55): Show |
G | 1 | a0001c0001t0001g0088 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-85-19902_-85-1984 others(66): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819070 | ||||||
chr5:60819074
|
GGGAGGGG others(53): Show |
G | 29 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0082others(26): Show | 29 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1984 others(64): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819074 | ||||||
chr5:60819079
|
GGGAGGGG others(48): Show |
G | 38 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0052others(35): Show | 39 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1985 others(59): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819079 | ||||||
chr5:60819084
|
GGGAGGGG others(43): Show |
G | 26 | a0001c0001t0001g0059a0001c0001t0002g0099a0001c0001t0003g0114others(23): Show | 27 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1985 others(54): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819084 | ||||||
chr5:60819085
|
GGAGGGGA others(40): Show |
G | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19902_-85-1985 others(51): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819085 | ||||||
chr5:60819089
|
GGGAGGGG others(13): Show |
G | 1 | a0001c0001t0008g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-19879_-85-1986 others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819089 | ||||||
chr5:60819089
|
GGGAGGGG others(38): Show |
G | 13 | a0001c0001t0001g0101a0001c0001t0005g0008a0001c0001t0005g0011others(10): Show | 14 | HG00738.hp1 HG01069.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1986 others(49): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819089 | ||||||
chr5:60819094
|
G | A | 6 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216others(3): Show | 6 | HG00621.hp1 HG03490.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-19864C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819094 | ||||||
chr5:60819094
|
G | GGGAGA | 3 | a0001c0001t0002g0229a0001c0001t0002g0235a0001c0001t0002g0236 | 3 | HG00735.hp2 HG01099.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-85-19865_-85-1986 others(9): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819094 | ||||||
chr5:60819094
|
GGGAGGGG others(33): Show |
G | 5 | a0001c0001t0005g0016a0001c0001t0007g0032a0001c0001t0007g0034others(2): Show | 5 | HG01192.hp2 HG01358.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1986 others(44): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819094 | ||||||
chr5:60819099
|
G | A | 18 | a0001c0001t0001g0140a0001c0001t0002g0213a0001c0001t0002g0214others(15): Show | 18 | HG00621.hp1 HG00735.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-19869C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
G | GGGAGAGG others(3): Show |
5 | a0001c0001t0002g0220a0001c0001t0002g0222a0001c0001t0002g0227others(2): Show | 5 | HG03471.hp2 NA18983.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-19879_-85-1987 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
G | GGGAGAGG others(8): Show |
1 | a0001c0001t0002g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-85-19884_-85-1987 others(19): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
G | GGGAGGGG others(3): Show |
3 | a0001c0001t0002g0228a0001c0001t0002g0230a0001c0001t0002g0242 | 3 | HG00639.hp2 HG01952.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-85-19870_-85-1986 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
G | GGGAGGGG others(13): Show |
2 | a0001c0001t0002g0232a0001c0001t0024g0217 | 2 | HG04204.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-85-19870_-85-1986 others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
G | GGGAGGGG others(18): Show |
1 | a0001c0001t0002g0239 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-85-19870_-85-1986 others(29): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
G | GGGAGGGG others(18): Show |
1 | a0001c0001t0002g0240 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-85-19870_-85-1986 others(29): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
GGGAGAGG others(3): Show |
G | 5 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0136others(2): Show | 5 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-19879_-85-1987 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
GGGAGAGG others(23): Show |
G | 2 | a0001c0001t0007g0030a0001c0001t0017g0035 | 2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-85-19899_-85-1987 others(34): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819099
|
GGGAGAGG others(28): Show |
G | 1 | a0001c0001t0007g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-85-19904_-85-1987 others(39): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | ||||||
chr5:60819109
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19879T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819109 | ||||||
chr5:60819114
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19884T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819114 | ||||||
chr5:60819119
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19889T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819119 | ||||||
chr5:60819124
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19894T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819124 | ||||||
chr5:60819129
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19899T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819129 | ||||||
chr5:60819133
|
G | T | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19903C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819133 | ||||||
chr5:60819134
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0168a0001c0001t0007g0030others(1): Show | 4 | HG01361.hp1 HG03927.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-19904T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819134 | ||||||
chr5:60819252
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-20022T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819252 | ||||||
chr5:60819374
|
G | A | 4 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-20144C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819374 | ||||||
chr5:60819546
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-85-20316G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819546 | ||||||
chr5:60819601
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-20371C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819601 | ||||||
chr5:60819639
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-85-20409G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819639 | ||||||
chr5:60819690
|
G | T | 1 | a0001c0001t0016g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-20460C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819690 | ||||||
chr5:60819840
|
G | A | 2 | a0001c0001t0005g0015a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-85-20610C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819840 | ||||||
chr5:60820170
|
G | C | 1 | a0001c0001t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-85-20940C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820170 | ||||||
chr5:60820260
|
T | C | 2 | a0001c0001t0006g0142a0001c0003t0006g0141 | 2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-85-21030A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820260 | ||||||
chr5:60820330
|
C | A | 2 | a0001c0001t0008g0137a0001c0001t0008g0138 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-85-21100G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820330 | ||||||
chr5:60820369
|
T | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0167 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-21139A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820369 | ||||||
chr5:60820586
|
C | T | 1 | a0001c0001t0016g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-21356G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820586 | ||||||
chr5:60820706
|
C | T | 24 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216others(21): Show | 24 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-85-21476G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820706 | ||||||
chr5:60820786
|
T | C | 9 | a0001c0001t0007g0001a0001c0001t0007g0030a0001c0001t0007g0031others(6): Show | 10 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85-21556A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820786 | ||||||
chr5:60820923
|
A | G | 1 | a0001c0001t0016g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-21693T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820923 | ||||||
chr5:60821053
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-85-21823G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821053 | ||||||
chr5:60821057
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-85-21827G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821057 | ||||||
chr5:60821282
|
T | G | 1 | a0001c0001t0004g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-85-22052A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821282 | ||||||
chr5:60821375
|
A | C | 1 | a0001c0001t0002g0189 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-85-22145T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821375 | ||||||
chr5:60821375
|
A | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(150): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-22145T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821375 | ||||||
chr5:60821654
|
T | C | 2 | a0001c0001t0012g0243a0001c0001t0012g0244 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-85-22424A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821654 | ||||||
chr5:60821679
|
A | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-85-22449T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821679 | ||||||
chr5:60821711
|
T | C | 1 | a0001c0001t0003g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-86+22449A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821711 | ||||||
chr5:60821896
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-86+22264A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821896 | ||||||
chr5:60822163
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-86+21997A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822163 | ||||||
chr5:60822284
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-86+21876C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822284 | ||||||
chr5:60822488
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-86+21672T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822488 | ||||||
chr5:60822936
|
C | T | 1 | a0001c0001t0024g0217 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-86+21224G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822936 | ||||||
chr5:60823010
|
A | G | 1 | a0001c0001t0019g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-86+21150T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823010 | ||||||
chr5:60823045
|
G | A | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+21115C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823045 | ||||||
chr5:60823058
|
GAGA | G | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+21099_-86+2110 others(7): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823058 | ||||||
chr5:60823134
|
T | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-86+21026A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823134 | ||||||
chr5:60823135
|
GAAGT | G | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-86+21021_-86+2102 others(8): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823135 | ||||||
chr5:60823205
|
A | C | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+20955T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823205 | ||||||
chr5:60823270
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-86+20890G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823270 | ||||||
chr5:60823271
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0006g0145a0001c0001t0006g0165others(3): Show | 6 | HG00099.hp1 HG01175.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+20889C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823271 | ||||||
chr5:60823360
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-86+20800C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823360 | ||||||
chr5:60823838
|
G | A | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+20322C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823838 | ||||||
chr5:60823897
|
G | C | 1 | a0001c0001t0004g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-86+20263C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823897 | ||||||
chr5:60823910
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-86+20250T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823910 | ||||||
chr5:60824072
|
A | T | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-86+20088T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824072 | ||||||
chr5:60824295
|
C | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(191): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-86+19865G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824295 | ||||||
chr5:60824362
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0008g0205 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-86+19798C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824362 | ||||||
chr5:60824384
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-86+19776C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824384 | ||||||
chr5:60824456
|
A | G | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+19704T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824456 | ||||||
chr5:60824867
|
T | A | 1 | a0001c0001t0003g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-86+19293A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824867 | ||||||
chr5:60824894
|
C | A | 1 | a0001c0001t0004g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-86+19266G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824894 | ||||||
chr5:60824963
|
T | TC | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-86+19196_-86+1919 others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824963 | ||||||
chr5:60825171
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0020g0130 | 3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+18989C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825171 | ||||||
chr5:60825270
|
A | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-86+18890T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825270 | ||||||
chr5:60825411
|
C | T | 32 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-86+18749G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825411 | ||||||
chr5:60825444
|
T | C | 37 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(34): Show | 38 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-86+18716A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825444 | ||||||
chr5:60825482
|
C | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+18678G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825482 | ||||||
chr5:60825535
|
G | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-86+18625C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825535 | ||||||
chr5:60825643
|
A | T | 9 | a0001c0001t0007g0001a0001c0001t0007g0030a0001c0001t0007g0031others(6): Show | 10 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-86+18517T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825643 | ||||||
chr5:60825647
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+18513C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825647 | ||||||
chr5:60826372
|
A | AT | 5 | a0001c0001t0006g0145a0001c0001t0006g0165a0001c0001t0006g0204others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+17787dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826372 | ||||||
chr5:60826374
|
T | A | 31 | a0001c0001t0001g0168a0001c0001t0005g0008a0001c0001t0005g0009others(28): Show | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+17786A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826374 | ||||||
chr5:60826557
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0019g0041 | 2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-86+17603C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826557 | ||||||
chr5:60826564
|
C | T | 1 | a0002c0002t0002g0109 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-86+17596G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826564 | ||||||
chr5:60826580
|
T | C | 1 | a0001c0001t0002g0239 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-86+17580A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826580 | ||||||
chr5:60826809
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0020g0130 | 3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+17351G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826809 | ||||||
chr5:60827047
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-86+17113T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827047 | ||||||
chr5:60827077
|
C | T | 5 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0012g0243others(2): Show | 5 | HG01192.hp1 HG01433.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+17083G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827077 | ||||||
chr5:60827156
|
C | T | 1 | a0001c0001t0017g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-86+17004G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827156 | ||||||
chr5:60827236
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-86+16924G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827236 | ||||||
chr5:60827454
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG01099.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-86+16706T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827454 | ||||||
chr5:60827934
|
C | T | 1 | a0001c0001t0024g0217 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-86+16226G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827934 | ||||||
chr5:60827956
|
G | A | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+16204C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827956 | ||||||
chr5:60827961
|
A | T | 1 | a0001c0001t0001g0069 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-86+16199T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827961 | ||||||
chr5:60828013
|
AC | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(188): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-86+16146delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828013 | ||||||
chr5:60828096
|
T | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0020g0130 | 3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+16064A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828096 | ||||||
chr5:60828178
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-86+15982G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828178 | ||||||
chr5:60828331
|
C | CTA | 3 | a0001c0001t0006g0165a0001c0001t0006g0204a0001c0001t0023g0164 | 3 | HG01175.hp2 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-86+15828_-86+1582 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828331 | ||||||
chr5:60828406
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-86+15754A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828406 | ||||||
chr5:60828453
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-86+15707A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828453 | ||||||
chr5:60828644
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+15516C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828644 | ||||||
chr5:60829014
|
A | G | 1 | a0001c0001t0013g0007 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-86+15146T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829014 | ||||||
chr5:60829110
|
T | A | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+15050A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829110 | ||||||
chr5:60829168
|
C | CA | 31 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(28): Show | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+14991dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829168 | ||||||
chr5:60829199
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+14961C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829199 | ||||||
chr5:60829203
|
C | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0099 | 2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-86+14957G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829203 | ||||||
chr5:60829277
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0167 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+14883C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829277 | ||||||
chr5:60829401
|
T | G | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+14759A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829401 | ||||||
chr5:60829463
|
A | G | 1 | a0001c0001t0003g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-86+14697T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829463 | ||||||
chr5:60829525
|
T | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+14635A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829525 | ||||||
chr5:60829615
|
T | C | 1 | a0001c0001t0006g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-86+14545A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829615 | ||||||
chr5:60830045
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+14115G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830045 | ||||||
chr5:60830439
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-86+13721A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830439 | ||||||
chr5:60830475
|
A | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 12 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+13685T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830475 | ||||||
chr5:60830597
|
T | C | 187 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(184): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-86+13563A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830597 | ||||||
chr5:60830609
|
CT | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0092others(9): Show | 13 | HG00280.hp1 HG00544.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+13550delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830609 | ||||||
chr5:60830613
|
T | C | 11 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(8): Show | 11 | HG00621.hp2 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+13547A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830613 | ||||||
chr5:60831232
|
G | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+12928C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831232 | ||||||
chr5:60831468
|
A | G | 3 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182 | 3 | HG01516.hp1 HG01517.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-86+12692T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831468 | ||||||
chr5:60831690
|
A | T | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+12470T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831690 | ||||||
chr5:60831842
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-86+12318G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831842 | ||||||
chr5:60831897
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(95): Show | 102 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-86+12263A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831897 | ||||||
chr5:60831976
|
A | C | 1 | a0001c0001t0002g0227 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-86+12184T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831976 | ||||||
chr5:60832366
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0122 | 3 | HG00639.hp1 HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-86+11794A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832366 | ||||||
chr5:60832370
|
T | G | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG03490.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-86+11790A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832370 | ||||||
chr5:60832652
|
T | A | 1 | a0001c0001t0004g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-86+11508A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832652 | ||||||
chr5:60832659
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-86+11501G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832659 | ||||||
chr5:60832662
|
C | T | 17 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(14): Show | 17 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-86+11498G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832662 | ||||||
chr5:60832813
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-86+11347C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832813 | ||||||
chr5:60833069
|
A | C | 1 | a0001c0001t0003g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-86+11091T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833069 | ||||||
chr5:60833186
|
T | C | 4 | a0001c0001t0005g0011a0001c0001t0005g0016a0001c0001t0005g0017others(1): Show | 4 | HG01069.hp2 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+10974A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833186 | ||||||
chr5:60833240
|
T | C | 1 | a0001c0001t0001g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-86+10920A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833240 | ||||||
chr5:60833501
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+10659C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833501 | ||||||
chr5:60833534
|
A | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-86+10626T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833534 | ||||||
chr5:60833594
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-86+10566T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833594 | ||||||
chr5:60833845
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-86+10315A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833845 | ||||||
chr5:60833868
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-86+10292A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833868 | ||||||
chr5:60833921
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG00438.hp1 HG00673.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+10239T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833921 | ||||||
chr5:60833956
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-86+10204T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833956 | ||||||
chr5:60834391
|
C | T | 1 | a0001c0001t0004g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-86+9769G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834391 | ||||||
chr5:60834540
|
C | T | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+9620G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834540 | ||||||
chr5:60834684
|
A | C | 1 | a0001c0001t0002g0002 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-86+9476T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834684 | ||||||
chr5:60834730
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-86+9430G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834730 | ||||||
chr5:60834775
|
G | A | 1 | a0001c0001t0008g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-86+9385C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834775 | ||||||
chr5:60834781
|
GT | G | 3 | a0001c0001t0005g0019a0001c0001t0005g0022a0001c0001t0015g0020 | 3 | HG02145.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-86+9378delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834781 | ||||||
chr5:60834786
|
TTGATTTT others(2459): Show |
T | 3 | a0001c0001t0005g0019a0001c0001t0005g0022a0001c0001t0015g0020 | 3 | HG02145.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-86+6908_-86+9373d others(2): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834786 | ||||||
chr5:60835008
|
C | T | 247 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(244): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-86+9152G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835008 | ||||||
chr5:60835020
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+9140C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835020 | ||||||
chr5:60835156
|
C | T | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+9004G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835156 | ||||||
chr5:60835190
|
G | GA | 17 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(14): Show | 17 | HG00438.hp2 HG01109.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-86+8969dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835190 | ||||||
chr5:60835190
|
GA | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG01069.hp2 HG01167.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8969delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835190 | ||||||
chr5:60835467
|
A | G | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8693T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835467 | ||||||
chr5:60835570
|
C | A | 1 | a0001c0001t0003g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-86+8590G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835570 | ||||||
chr5:60835824
|
C | T | 28 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 29 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-86+8336G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835824 | ||||||
chr5:60835930
|
C | G | 1 | a0001c0001t0005g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-86+8230G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835930 | ||||||
chr5:60835989
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-86+8171G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835989 | ||||||
chr5:60836016
|
G | A | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8144C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836016 | ||||||
chr5:60836057
|
T | C | 28 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 29 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-86+8103A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836057 | ||||||
chr5:60836119
|
A | C | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8041T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836119 | ||||||
chr5:60836142
|
C | CAT | 104 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(101): Show | 108 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.-86+8016_-86+8017d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836142 | ||||||
chr5:60836285
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-86+7875C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836285 | ||||||
chr5:60836358
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+7802A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836358 | ||||||
chr5:60837253
|
T | A | 3 | a0001c0001t0005g0019a0001c0001t0005g0022a0001c0001t0015g0020 | 3 | HG02145.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-86+6907A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837253 | ||||||
chr5:60837290
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-86+6870C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837290 | ||||||
chr5:60837297
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-86+6863G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837297 | ||||||
chr5:60837313
|
GGTGGGGG others(4): Show |
G | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+6836_-86+6846d others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837313 | ||||||
chr5:60837314
|
GTGGGGGG others(3): Show |
G | 1 | a0001c0001t0005g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-86+6836_-86+6845d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837314 | ||||||
chr5:60837315
|
T | G | 11 | a0001c0001t0001g0045a0001c0001t0001g0108a0001c0001t0001g0167others(8): Show | 11 | HG00621.hp2 HG01261.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+6845A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | ||||||
chr5:60837315
|
T | TG | 79 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0058others(76): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-86+6844dupC | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | ||||||
chr5:60837315
|
T | TGG | 37 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104others(34): Show | 39 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-86+6843_-86+6844d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | ||||||
chr5:60837315
|
T | TGGG | 16 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0151others(13): Show | 16 | HG01109.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-86+6842_-86+6844d others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | ||||||
chr5:60837315
|
T | TGGGG | 15 | a0001c0001t0001g0107a0001c0001t0003g0155a0001c0001t0003g0156others(12): Show | 15 | HG01109.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-86+6841_-86+6844d others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | ||||||
chr5:60837315
|
T | TGGGGGGG others(4): Show |
1 | a0001c0001t0003g0192 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-86+6844_-86+6845i others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | ||||||
chr5:60837322
|
GGAGTGGG others(4): Show |
G | 1 | a0001c0001t0020g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-86+6827_-86+6837d others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837322 | ||||||
chr5:60837324
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(199): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-86+6836T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837324 | ||||||
chr5:60837324
|
A | T | 1 | a0001c0001t0003g0192 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-86+6836T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837324 | ||||||
chr5:60837325
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0009g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-86+6834_-86+6835i others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837325 | ||||||
chr5:60837326
|
T | G | 14 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0127others(11): Show | 14 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.-86+6834A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837326 | ||||||
chr5:60837332
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0003g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-86+6827_-86+6828i others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837332 | ||||||
chr5:60837333
|
T | C | 2 | a0001c0001t0002g0206a0001c0001t0008g0205 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-86+6827A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837333 | ||||||
chr5:60837333
|
T | G | 11 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0003g0006others(8): Show | 12 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-86+6827A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837333 | ||||||
chr5:60837465
|
G | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-86+6695C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837465 | ||||||
chr5:60837866
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0008g0205 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-86+6294G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837866 | ||||||
chr5:60837880
|
A | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-86+6280T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837880 | ||||||
chr5:60838290
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-86+5870C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838290 | ||||||
chr5:60838462
|
A | G | 1 | a0001c0001t0003g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-86+5698T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838462 | ||||||
chr5:60838513
|
G | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0020g0130 | 3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+5647C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838513 | ||||||
chr5:60838541
|
C | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+5619G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838541 | ||||||
chr5:60838550
|
A | C | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+5610T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838550 | ||||||
chr5:60838811
|
G | A | 19 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(16): Show | 19 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86+5349C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838811 | ||||||
chr5:60838852
|
C | T | 2 | a0001c0001t0003g0161a0001c0001t0004g0047 | 2 | HG02818.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-86+5308G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838852 | ||||||
chr5:60838950
|
G | A | 6 | a0001c0001t0001g0173a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG02145.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+5210C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838950 | ||||||
chr5:60839021
|
CAA | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(163): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-86+5137_-86+5138d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839021 | ||||||
chr5:60839027
|
A | T | 2 | a0001c0001t0003g0169a0001c0001t0003g0170 | 2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-86+5133T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839027 | ||||||
chr5:60839029
|
A | T | 52 | a0001c0001t0001g0140a0001c0001t0001g0173a0001c0001t0001g0198others(49): Show | 53 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.-86+5131T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839029 | ||||||
chr5:60839031
|
T | A | 12 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0166others(9): Show | 12 | HG01175.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+5129A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839031 | ||||||
chr5:60839033
|
T | A | 5 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+5127A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839033 | ||||||
chr5:60839044
|
A | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+5116T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839044 | ||||||
chr5:60839294
|
G | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-86+4866C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839294 | ||||||
chr5:60839355
|
G | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(6): Show | 9 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+4805C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839355 | ||||||
chr5:60839685
|
G | A | 1 | a0001c0001t0004g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-86+4475C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839685 | ||||||
chr5:60840037
|
G | A | 1 | a0001c0001t0006g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-86+4123C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840037 | ||||||
chr5:60840132
|
G | C | 2 | a0001c0001t0008g0137a0001c0001t0008g0138 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-86+4028C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840132 | ||||||
chr5:60840135
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(88): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+4025C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840135 | ||||||
chr5:60840158
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(168): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-86+4002T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840158 | ||||||
chr5:60840286
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-86+3874A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840286 | ||||||
chr5:60840627
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(88): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+3533G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840627 | ||||||
chr5:60840700
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0167 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+3460G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840700 | ||||||
chr5:60840741
|
A | T | 19 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0003g0038others(16): Show | 19 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86+3419T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840741 | ||||||
chr5:60840786
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-86+3374G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840786 | ||||||
chr5:60840799
|
G | A | 10 | a0001c0001t0007g0001a0001c0001t0007g0028a0001c0001t0007g0030others(7): Show | 11 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-86+3361C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840799 | ||||||
chr5:60841006
|
T | TA | 19 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0003g0038others(16): Show | 19 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86+3153dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841006 | ||||||
chr5:60841023
|
C | CT | 5 | a0001c0001t0001g0045a0001c0001t0001g0218a0001c0001t0009g0245others(2): Show | 5 | HG01981.hp1 HG02135.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+3136dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841023 | ||||||
chr5:60841023
|
CT | C | 96 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-86+3136delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841023 | ||||||
chr5:60841023
|
CTT | C | 7 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-86+3135_-86+3136d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841023 | ||||||
chr5:60841075
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-86+3085C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841075 | ||||||
chr5:60841309
|
A | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0020g0130 | 3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+2851T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841309 | ||||||
chr5:60841341
|
A | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-86+2819T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841341 | ||||||
chr5:60841423
|
A | G | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2737T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841423 | ||||||
chr5:60841426
|
A | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2734T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841426 | ||||||
chr5:60841433
|
T | A | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2727A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841433 | ||||||
chr5:60841435
|
A | T | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2725T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841435 | ||||||
chr5:60841437
|
T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2723A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841437 | ||||||
chr5:60841438
|
G | A | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2722C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841438 | ||||||
chr5:60841439
|
G | A | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2721C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841439 | ||||||
chr5:60841440
|
G | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2720C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841440 | ||||||
chr5:60841441
|
T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2719A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841441 | ||||||
chr5:60841443
|
T | A | 205 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(202): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-86+2717A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841443 | ||||||
chr5:60841448
|
T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2712A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841448 | ||||||
chr5:60841450
|
T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2710A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841450 | ||||||
chr5:60841467
|
T | G | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2693A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841467 | ||||||
chr5:60841468
|
CTTATCCT others(4): Show |
C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2681_-86+2691d others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841468 | ||||||
chr5:60841480
|
G | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2680C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841480 | ||||||
chr5:60841561
|
G | A | 1 | a0001c0001t0001g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-86+2599C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841561 | ||||||
chr5:60841674
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-86+2486A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841674 | ||||||
chr5:60841778
|
T | C | 3 | a0001c0001t0003g0201a0001c0001t0011g0202a0001c0001t0011g0203 | 3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-86+2382A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841778 | ||||||
chr5:60842003
|
G | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-86+2157C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842003 | ||||||
chr5:60842032
|
C | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-86+2128G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842032 | ||||||
chr5:60842132
|
A | G | 39 | a0001c0001t0001g0173a0001c0001t0001g0198a0001c0001t0001g0199others(36): Show | 40 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.-86+2028T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842132 | ||||||
chr5:60842146
|
A | C | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-86+2014T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842146 | ||||||
chr5:60842233
|
T | C | 1 | a0001c0001t0006g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-86+1927A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842233 | ||||||
chr5:60842460
|
A | T | 7 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0134others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+1700T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842460 | ||||||
chr5:60842496
|
T | TA | 12 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0125others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-86+1663dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842496 | ||||||
chr5:60842496
|
T | TAA | 92 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0045others(89): Show | 96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.-86+1662_-86+1663d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842496 | ||||||
chr5:60842512
|
G | T | 31 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(28): Show | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+1648C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842512 | ||||||
chr5:60842516
|
GCAGGGGG others(1): Show |
G | 10 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(7): Show | 10 | HG03490.hp2 HG03491.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.-86+1636_-86+1643d others(10): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842516 | ||||||
chr5:60842763
|
C | T | 39 | a0001c0001t0001g0173a0001c0001t0001g0198a0001c0001t0001g0199others(36): Show | 40 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.-86+1397G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842763 | ||||||
chr5:60842866
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1294A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842866 | ||||||
chr5:60842869
|
G | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1291C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842869 | ||||||
chr5:60842874
|
T | A | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1286A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842874 | ||||||
chr5:60842875
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1285C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842875 | ||||||
chr5:60842880
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1280G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842880 | ||||||
chr5:60842881
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1279A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842881 | ||||||
chr5:60842885
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1275G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842885 | ||||||
chr5:60842886
|
A | G | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1274T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842886 | ||||||
chr5:60842887
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0019g0041 | 2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-86+1273G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842887 | ||||||
chr5:60842891
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1269A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842891 | ||||||
chr5:60842892
|
A | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1268T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842892 | ||||||
chr5:60842895
|
T | A | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1265A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842895 | ||||||
chr5:60842897
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1263A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842897 | ||||||
chr5:60842900
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1260C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842900 | ||||||
chr5:60842901
|
C | A | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1259G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842901 | ||||||
chr5:60842902
|
C | G | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1258G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842902 | ||||||
chr5:60842903
|
A | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1257T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842903 | ||||||
chr5:60842904
|
C | CGTAGGGC others(1): Show |
91 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(88): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+1255_-86+1256i others(10): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842904 | ||||||
chr5:60842905
|
G | T | 1 | a0001c0001t0003g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1255C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842905 | ||||||
chr5:60843022
|
C | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86+1138G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843022 | ||||||
chr5:60843056
|
C | G | 11 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+1104G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843056 | ||||||
chr5:60843064
|
G | A | 1 | a0001c0001t0025g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+1096C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843064 | ||||||
chr5:60843128
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-86+1032G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843128 | ||||||
chr5:60843211
|
G | C | 2 | a0001c0001t0006g0165a0001c0001t0023g0164 | 2 | HG01175.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-86+949C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843211 | ||||||
chr5:60843233
|
G | A | 4 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(1): Show | 4 | HG01099.hp2 HG01168.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+927C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843233 | ||||||
chr5:60843259
|
C | T | 2 | a0001c0001t0003g0169a0001c0001t0003g0170 | 2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-86+901G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843259 | ||||||
chr5:60843336
|
G | GGGGAAAG others(19): Show |
1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+798_-86+823dup others(26): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843336 | ||||||
chr5:60843336
|
GGGGAAAG others(19): Show |
G | 31 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(28): Show | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+798_-86+823del others(26): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843336 | ||||||
chr5:60843337
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-86+823C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843337 | ||||||
chr5:60843391
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-86+769C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843391 | ||||||
chr5:60843721
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(88): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+439G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843721 | ||||||
chr5:60843727
|
C | G | 1 | a0001c0001t0003g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-86+433G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843727 | ||||||
chr5:60843909
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-86+251C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843909 | ||||||
chr5:60843965
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-86+195C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843965 | ||||||
chr5:60844048
|
C | T | 1 | a0001c0001t0004g0037 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-86+112G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60844048 | ||||||
chr5:60844054
|
A | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(135): Show | 142 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86+106T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60844054 |