geneid | 9092 |
---|---|
ensemblid | ENSG00000175467.15 |
hgncid | 10538 |
symbol | SART1 |
name | spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP |
refseq_nuc | NM_005146.5 |
refseq_prot | NP_005137.1 |
ensembl_nuc | ENST00000312397.10 |
ensembl_prot | ENSP00000310448.5 |
mane_status | MANE Select |
chr | chr11 |
start | 65961734 |
end | 65980137 |
strand | + |
ver | v1.2 |
region | chr11:65961734-65980137 |
region5000 | chr11:65956734-65985137 |
regionname0 | SART1_chr11_65961734_65980137 |
regionname5000 | SART1_chr11_65956734_65985137 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 800 | 220 | 86 | 30 | 70 | 7 | 25 | 48 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002 | 0/0 | 800 | 151 | 5 | 38 | 87 | 5 | 16 | 61 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0003 | 0/0 | 800 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0004 | 0/0 | 800 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0005 | 0/0 | 800 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0006 | 0/0 | 800 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0007 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0008 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0009 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0010 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0011 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2403 | 149 | 5 | 37 | 86 | 5 | 16 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0002 | 0/1 | 2403 | 111 | 24 | 23 | 31 | 7 | 25 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0003 | 1/0 | 2403 | 46 | 26 | 3 | 16 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0004 | 0/0 | 2403 | 29 | 6 | 1 | 22 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0005 | 0/0 | 2403 | 24 | 22 | 2 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0006 | 0/0 | 2403 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0007 | 0/0 | 2403 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0008 | 0/0 | 2403 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0009 | 0/0 | 2403 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0010 | 0/0 | 2403 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0011 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0012 | 0/0 | 2403 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0013 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0014 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0015 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0016 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0017 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0018 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0019 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0020 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0021 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
c0022 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1155 | 174 | 23 | 40 | 88 | 5 | 18 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0002 | 0/0 | 1155 | 116 | 44 | 12 | 45 | 3 | 12 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0003 | 0/1 | 1155 | 64 | 8 | 13 | 28 | 4 | 10 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0004 | 0/0 | 1154 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0005 | 1/0 | 1155 | 5 | 4 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0006 | 0/0 | 1155 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0007 | 0/0 | 1155 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0008 | 0/0 | 1155 | 2 | 1 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0009 | 0/0 | 1155 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0010 | 0/0 | 1154 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0011 | 0/0 | 1155 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0012 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0013 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0014 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0015 | 0/0 | 1155 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0016 | 0/0 | 1155 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0017 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
t0018 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 29 | 1 | 8 | 12 | 0 | 8 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0002 | 0/0 | 14 | 0 | 3 | 9 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0003 | 0/0 | 12 | 0 | 8 | 4 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0006 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0008 | 0/0 | 5 | 1 | 1 | 1 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0010 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0039 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/1 | 2403 | 111 | 24 | 23 | 31 | 7 | 25 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003 | 1/0 | 2403 | 46 | 26 | 3 | 16 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0004 | 0/0 | 2403 | 29 | 6 | 1 | 22 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0005 | 0/0 | 2403 | 24 | 22 | 2 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0006 | 0/0 | 2403 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0007 | 0/0 | 2403 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0016 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0017 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0019 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0021 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0001 | 0/0 | 2403 | 149 | 5 | 37 | 86 | 5 | 16 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0011 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0012 | 0/0 | 2403 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0003c0008 | 0/0 | 2403 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0004c0009 | 0/0 | 2403 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0005c0010 | 0/0 | 2403 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0006c0022 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0007c0014 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0008c0013 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0009c0018 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0010c0015 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0011c0020 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 3557 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0002 | 0/0 | 3557 | 49 | 22 | 9 | 3 | 3 | 12 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0003 | 0/1 | 3557 | 54 | 1 | 12 | 26 | 4 | 10 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0008 | 0/0 | 3557 | 2 | 1 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0009 | 0/0 | 3557 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0011 | 0/0 | 3557 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0012 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0002t0013 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003t0002 | 0/0 | 3557 | 23 | 6 | 1 | 16 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003t0003 | 0/0 | 3557 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003t0004 | 0/0 | 3556 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003t0005 | 1/0 | 3557 | 5 | 4 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003t0010 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0003t0015 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0004t0002 | 0/0 | 3557 | 23 | 1 | 1 | 21 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0004t0006 | 0/0 | 3557 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0004t0007 | 0/0 | 3557 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0004t0014 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0005t0001 | 0/0 | 3557 | 16 | 15 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0005t0002 | 0/0 | 3557 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0006t0001 | 0/0 | 3557 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0007t0002 | 0/0 | 3557 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0016t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0017t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0019t0002 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0001c0021t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0001t0001 | 0/0 | 3557 | 146 | 5 | 37 | 84 | 5 | 15 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0001t0016 | 0/0 | 3557 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0001t0017 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0001t0018 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0011t0001 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0002c0012t0001 | 0/0 | 3557 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0003c0008t0002 | 0/0 | 3557 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0004c0009t0001 | 0/0 | 3557 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0005c0010t0003 | 0/0 | 3557 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0006c0022t0001 | 0/0 | 3557 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0007c0014t0001 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0008c0013t0001 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0009c0018t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0010c0015t0002 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
a0011c0020t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | copy fasta | chr11 | 65956734 | 65985137 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0010 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0002 | 0/0 | 13 | 0 | 3 | 8 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0039 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0009g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0011g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0012g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0002t0013g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0004g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0005g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0003t0015g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0004t0014g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0005t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0007t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0007t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0016t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0017t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0019t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0001c0021t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0001 | 0/0 | 24 | 1 | 7 | 9 | 0 | 7 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0003 | 0/0 | 12 | 0 | 8 | 4 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0017g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0001t0018g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0002c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0003c0008t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0003c0008t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0003c0008t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0004c0009t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0005c0010t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0005c0010t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0006c0022t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0007c0014t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0008c0013t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0009c0018t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0010c0015t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
a0011c0020t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0097 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0077 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00140 | hp1 | a0002 | c0001 | t0001 | g0078 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0213 | EUR | FIN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | FIN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00423 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0140 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00558 | hp1 | a0001 | c0003 | t0002 | g0258 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00597 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00621 | hp2 | a0001 | c0003 | t0002 | g0192 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0023 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00673 | hp1 | a0001 | c0004 | t0014 | g0053 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00673 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00735 | hp2 | a0002 | c0001 | t0001 | g0024 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00738 | hp1 | a0002 | c0001 | t0001 | g0107 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01069 | hp2 | a0002 | c0001 | t0001 | g0025 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01070 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01071 | hp2 | a0002 | c0001 | t0001 | g0025 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01074 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01081 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0253 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01099 | hp2 | a0001 | c0002 | t0011 | g0226 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01106 | hp1 | a0001 | c0005 | t0002 | g0042 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0162 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01109 | hp2 | a0001 | c0006 | t0001 | g0143 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0114 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0229 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01169 | hp2 | a0002 | c0001 | t0001 | g0113 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0251 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01175 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0153 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01243 | hp1 | a0001 | c0003 | t0004 | g0013 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01243 | hp2 | a0001 | c0003 | t0003 | g0064 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01255 | hp1 | a0002 | c0012 | t0001 | g0001 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01257 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0082 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0223 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0257 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01358 | hp2 | a0002 | c0001 | t0001 | g0152 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01361 | hp1 | a0002 | c0001 | t0001 | g0075 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0212 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01496 | hp2 | a0001 | c0002 | t0008 | g0202 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0008 | EUR | IBS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0010 | EUR | IBS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01884 | hp1 | a0001 | c0003 | t0010 | g0177 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01891 | hp1 | a0001 | c0007 | t0002 | g0017 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01891 | hp2 | a0002 | c0001 | t0001 | g0073 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01934 | hp1 | a0001 | c0005 | t0001 | g0007 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01934 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01975 | hp2 | a0002 | c0001 | t0001 | g0074 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01978 | hp1 | a0002 | c0001 | t0001 | g0105 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0076 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01981 | hp2 | a0002 | c0001 | t0001 | g0120 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0092 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02004 | hp2 | a0002 | c0001 | t0001 | g0134 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02027 | hp2 | a0001 | c0002 | t0013 | g0209 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0256 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02055 | hp2 | a0001 | c0004 | t0006 | g0045 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0014 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02074 | hp2 | a0001 | c0004 | t0002 | g0019 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02080 | hp1 | a0001 | c0004 | t0002 | g0004 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02080 | hp2 | a0001 | c0004 | t0002 | g0044 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02083 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0230 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0039 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02129 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0234 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0125 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02135 | hp2 | a0002 | c0001 | t0018 | g0098 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0065 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02155 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02155 | hp2 | a0001 | c0004 | t0002 | g0018 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02257 | hp1 | a0002 | c0001 | t0001 | g0112 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02257 | hp2 | a0001 | c0004 | t0007 | g0068 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02258 | hp1 | a0001 | c0003 | t0004 | g0167 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02258 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02273 | hp1 | a0002 | c0001 | t0001 | g0127 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02273 | hp2 | a0001 | c0004 | t0002 | g0020 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02280 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0160 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0187 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02293 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0247 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0156 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02523 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02572 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02572 | hp2 | a0001 | c0003 | t0003 | g0063 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0250 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0259 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02630 | hp2 | a0001 | c0005 | t0001 | g0022 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02647 | hp2 | a0001 | c0005 | t0001 | g0159 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0252 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0217 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02717 | hp1 | a0001 | c0005 | t0002 | g0262 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02723 | hp1 | a0002 | c0001 | t0001 | g0154 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02723 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02735 | hp1 | a0006 | c0022 | t0001 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02735 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02738 | hp1 | a0002 | c0001 | t0016 | g0091 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0146 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02809 | hp1 | a0001 | c0005 | t0002 | g0260 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02809 | hp2 | a0001 | c0006 | t0001 | g0141 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0022 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02895 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02895 | hp2 | a0002 | c0001 | t0001 | g0101 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02922 | hp2 | a0001 | c0005 | t0002 | g0263 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02970 | hp1 | a0001 | c0005 | t0002 | g0041 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02970 | hp2 | a0001 | c0004 | t0006 | g0047 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02976 | hp1 | a0001 | c0003 | t0005 | g0186 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02976 | hp2 | a0001 | c0017 | t0002 | g0161 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03017 | hp2 | a0001 | c0002 | t0009 | g0248 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03041 | hp1 | a0001 | c0003 | t0015 | g0021 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03041 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03098 | hp2 | a0001 | c0006 | t0001 | g0142 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03130 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03130 | hp2 | a0001 | c0007 | t0002 | g0048 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0180 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03139 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03195 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0060 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03225 | hp1 | a0001 | c0003 | t0004 | g0166 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0040 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03453 | hp1 | a0007 | c0014 | t0001 | g0157 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03453 | hp2 | a0001 | c0003 | t0005 | g0184 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03486 | hp1 | a0001 | c0003 | t0002 | g0164 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0228 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03491 | hp2 | a0002 | c0001 | t0001 | g0116 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0059 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03516 | hp2 | a0001 | c0003 | t0002 | g0163 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03540 | hp1 | a0001 | c0005 | t0002 | g0041 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0158 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03579 | hp2 | a0001 | c0003 | t0005 | g0185 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03654 | hp1 | a0001 | c0002 | t0003 | g0211 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03688 | hp2 | a0002 | c0001 | t0001 | g0079 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0084 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03704 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03710 | hp1 | a0001 | c0002 | t0003 | g0249 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0024 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0244 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03927 | hp2 | a0002 | c0001 | t0001 | g0111 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0237 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04115 | hp1 | a0002 | c0001 | t0001 | g0080 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0233 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0224 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18522 | hp1 | a0001 | c0004 | t0007 | g0069 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0182 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0083 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0198 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18906 | hp2 | a0001 | c0007 | t0002 | g0017 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18942 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18944 | hp1 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18944 | hp2 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18945 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0189 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18947 | hp2 | a0001 | c0019 | t0002 | g0014 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18948 | hp2 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18949 | hp1 | a0001 | c0004 | t0002 | g0058 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18949 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18950 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18950 | hp2 | a0003 | c0008 | t0002 | g0052 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18951 | hp1 | a0002 | c0001 | t0001 | g0100 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18954 | hp2 | a0008 | c0013 | t0001 | g0089 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18960 | hp1 | a0004 | c0009 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18960 | hp2 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18961 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18967 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18968 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0254 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18969 | hp1 | a0002 | c0001 | t0001 | g0129 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18969 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18971 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18971 | hp2 | a0005 | c0010 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18973 | hp1 | a0001 | c0002 | t0003 | g0255 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18973 | hp2 | a0001 | c0004 | t0002 | g0043 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18974 | hp1 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18974 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18975 | hp1 | a0001 | c0004 | t0002 | g0054 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18975 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18978 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18978 | hp2 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18980 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18983 | hp1 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18983 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18984 | hp1 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18984 | hp2 | a0003 | c0008 | t0002 | g0051 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18985 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18985 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0197 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18986 | hp2 | a0010 | c0015 | t0002 | g0020 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18988 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18989 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18989 | hp2 | a0003 | c0008 | t0002 | g0050 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18992 | hp1 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18992 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18993 | hp1 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18993 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18999 | hp1 | a0002 | c0011 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18999 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19001 | hp1 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19001 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0081 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19003 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19004 | hp2 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19005 | hp1 | a0001 | c0004 | t0002 | g0018 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19009 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19011 | hp1 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19011 | hp2 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0057 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19030 | hp2 | a0001 | c0005 | t0002 | g0261 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0178 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19054 | hp1 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19054 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19060 | hp1 | a0001 | c0004 | t0002 | g0055 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19060 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19063 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19063 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19064 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19066 | hp2 | a0004 | c0009 | t0001 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19070 | hp1 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19070 | hp2 | a0001 | c0002 | t0012 | g0008 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19074 | hp1 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19075 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19075 | hp2 | a0001 | c0004 | t0002 | g0056 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19077 | hp2 | a0002 | c0001 | t0017 | g0155 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19080 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19081 | hp1 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19081 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19084 | hp1 | a0001 | c0004 | t0002 | g0049 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19084 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19086 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19087 | hp2 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0245 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19088 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19089 | hp1 | a0005 | c0010 | t0003 | g0242 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19089 | hp2 | a0001 | c0004 | t0002 | g0070 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19090 | hp1 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19090 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19240 | hp1 | a0001 | c0003 | t0004 | g0168 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA19240 | hp2 | a0001 | c0003 | t0002 | g0067 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20129 | hp1 | a0001 | c0021 | t0002 | g0008 | AFR | ASW | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20129 | hp2 | a0001 | c0016 | t0002 | g0066 | AFR | ASW | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0090 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0023 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0002 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0034 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20905 | hp1 | a0002 | c0001 | t0001 | g0110 | SAS | GIH | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0040 | SAS | GIH | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0115 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02109 | hp1 | a0001 | c0003 | t0003 | g0061 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0236 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02486 | hp2 | a0001 | c0004 | t0006 | g0046 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02559 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03471 | hp1 | a0009 | c0018 | t0002 | g0179 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG03471 | hp2 | a0011 | c0020 | t0002 | g0169 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG06807 | hp1 | a0001 | c0002 | t0008 | g0205 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18955 | hp1 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA18955 | hp2 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20300 | hp1 | a0001 | c0003 | t0005 | g0183 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0165 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0062 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
NA21309 | hp2 | a0001 | c0005 | t0002 | g0264 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0039 | REF | REF | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0005 | g0188 | REF | REF | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:65962042
|
C | G | 1 | a0006 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.262C>G | p.Pro88Ala | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/20 | 309/3557 | 262/2403 | 88/800 | chr11 | 65962042 | ||
chr11:65966214
|
C | T | 1 | a0011 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.977C>T | p.Ala326Val | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 8/20 | 1024/3557 | 977/2403 | 326/800 | chr11 | 65966214 | ||
chr11:65966521
|
C | T | 1 | a0003 | 3 | NA18950.hp2 NA18984.hp2 NA18989.hp2 |
missense_variant | MODERATE | c.1153C>T | p.Arg385Trp | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/20 | 1200/3557 | 1153/2403 | 385/800 | chr11 | 65966521 | ||
chr11:65967490
|
C | T | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1333C>T | p.Arg445Cys | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1380/3557 | 1333/2403 | 445/800 | chr11 | 65967490 | ||
chr11:65967542
|
C | T | 1 | a0008 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1385C>T | p.Pro462Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1432/3557 | 1385/2403 | 462/800 | chr11 | 65967542 | ||
chr11:65967557
|
G | T | 1 | a0009 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1400G>T | p.Arg467Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1447/3557 | 1400/2403 | 467/800 | chr11 | 65967557 | ||
chr11:65967703
|
G | C | 4 | a0002a0004a0006others(1): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
missense_variant | MODERATE | c.1454G>C | p.Gly485Ala | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1501/3557 | 1454/2403 | 485/800 | chr11 | 65967703 | ||
chr11:65967735
|
G | A | 1 | a0010 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.1486G>A | p.Glu496Lys | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1533/3557 | 1486/2403 | 496/800 | chr11 | 65967735 | ||
chr11:65967781
|
A | G | 1 | a0005 | 2 | NA18971.hp2 NA19089.hp1 |
missense_variant | MODERATE | c.1532A>G | p.Gln511Arg | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1579/3557 | 1532/2403 | 511/800 | chr11 | 65967781 | ||
chr11:65976671
|
G | A | 1 | a0004 | 2 | NA18960.hp1 NA19066.hp2 |
missense_variant | MODERATE | c.1762G>A | p.Glu588Lys | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/20 | 1809/3557 | 1762/2403 | 588/800 | chr11 | 65976671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:65965180
|
G | A | 9 | a0001c0005a0001c0006a0002c0001others(6): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
synonymous_variant | LOW | c.516G>A | p.Ala172Ala | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/20 | 563/3557 | 516/2403 | 172/800 | chr11 | 65965180 | ||
chr11:65965922
|
C | T | 3 | a0001c0002a0001c0021a0005c0010 | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
synonymous_variant | LOW | c.774C>T | p.Thr258Thr | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 7/20 | 821/3557 | 774/2403 | 258/800 | chr11 | 65965922 | ||
chr11:65967348
|
C | T | 1 | a0001c0019 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.1278C>T | p.Leu426Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 10/20 | 1325/3557 | 1278/2403 | 426/800 | chr11 | 65967348 | ||
chr11:65967543
|
G | A | 1 | a0001c0021 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1386G>A | p.Pro462Pro | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1433/3557 | 1386/2403 | 462/800 | chr11 | 65967543 | ||
chr11:65967746
|
G | A | 2 | a0001c0006a0001c0007 | 6 | HG01109.hp2 HG01891.hp1 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.1497G>A | p.Leu499Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1544/3557 | 1497/2403 | 499/800 | chr11 | 65967746 | ||
chr11:65976481
|
C | T | 1 | a0002c0012 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.1659C>T | p.Phe553Phe | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 13/20 | 1706/3557 | 1659/2403 | 553/800 | chr11 | 65976481 | ||
chr11:65977061
|
T | C | 1 | a0001c0016 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1905T>C | p.Asn635Asn | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/20 | 1952/3557 | 1905/2403 | 635/800 | chr11 | 65977061 | ||
chr11:65978665
|
G | T | 5 | a0001c0004a0001c0007a0001c0016others(2): Show | 37 | HG00673.hp1 HG01891.hp1 HG02055.hp2 others(34): Show |
synonymous_variant | LOW | c.2238G>T | p.Arg746Arg | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/20 | 2285/3557 | 2238/2403 | 746/800 | chr11 | 65978665 | ||
chr11:65978816
|
C | T | 1 | a0002c0011 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2286C>T | p.Ser762Ser | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/20 | 2333/3557 | 2286/2403 | 762/800 | chr11 | 65978816 | ||
chr11:65978819
|
C | T | 1 | a0001c0017 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2289C>T | p.Asp763Asp | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/20 | 2336/3557 | 2289/2403 | 763/800 | chr11 | 65978819 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:65979182
|
A | G | 13 | a0001c0002t0001a0001c0005t0001a0001c0006t0001others(10): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*152A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 152 | chr11 | 65979182 | |||||
chr11:65979274
|
C | T | 1 | a0001c0002t0008 | 2 | HG01496.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*244C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 244 | chr11 | 65979274 | |||||
chr11:65979331
|
G | T | 1 | a0001c0004t0007 | 2 | HG02257.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*301G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 301 | chr11 | 65979331 | |||||
chr11:65979346
|
C | T | 1 | a0001c0003t0015 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 316 | chr11 | 65979346 | |||||
chr11:65979347
|
G | C | 2 | a0001c0002t0009a0001c0004t0007 | 3 | HG02257.hp2 HG03017.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*317G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 317 | chr11 | 65979347 | |||||
chr11:65979451
|
C | T | 1 | a0002c0001t0018 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 421 | chr11 | 65979451 | |||||
chr11:65979515
|
T | C | 1 | a0001c0003t0010 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 485 | chr11 | 65979515 | |||||
chr11:65979586
|
G | A | 5 | a0001c0002t0003a0001c0002t0009a0001c0003t0003others(2): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*556G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 556 | chr11 | 65979586 | |||||
chr11:65979609
|
A | G | 1 | a0001c0004t0006 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*579A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 579 | chr11 | 65979609 | |||||
chr11:65979614
|
C | T | 1 | a0001c0004t0014 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 584 | chr11 | 65979614 | |||||
chr11:65979723
|
T | C | 40 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(37): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
3_prime_UTR_variant | MODIFIER | c.*693T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 693 | chr11 | 65979723 | |||||
chr11:65979782
|
T | C | 1 | a0001c0002t0011 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 752 | chr11 | 65979782 | |||||
chr11:65979872
|
G | A | 1 | a0002c0001t0016 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 842 | chr11 | 65979872 | |||||
chr11:65979986
|
G | A | 1 | a0002c0001t0017 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*956G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 956 | chr11 | 65979986 | |||||
chr11:65980002
|
A | G | 1 | a0001c0002t0013 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 972 | chr11 | 65980002 | |||||
chr11:65980035
|
C | T | 1 | a0001c0002t0012 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 1005 | chr11 | 65980035 | |||||
chr11:65980110
|
CA | C | 2 | a0001c0003t0004a0001c0003t0010 | 9 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1088delA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 1088 | INFO_REALIGN_3_PRIME | chr11 | 65980110 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:65962204
|
G | A | 1 | a0001c0005t0002g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.313+111G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962204 | ||||||
chr11:65962206
|
T | C | 36 | a0001c0003t0002g0067a0001c0003t0003g0021a0001c0003t0003g0059others(33): Show | 47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.313+113T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962206 | ||||||
chr11:65962209
|
T | C | 36 | a0001c0003t0002g0067a0001c0003t0003g0021a0001c0003t0003g0059others(33): Show | 47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.313+116T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962209 | ||||||
chr11:65962381
|
C | T | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313+288C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962381 | ||||||
chr11:65962396
|
G | A | 1 | a0001c0005t0001g0022 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.313+303G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962396 | ||||||
chr11:65962507
|
G | T | 6 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(3): Show | 7 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.313+414G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962507 | ||||||
chr11:65962531
|
C | A | 102 | a0001c0006t0001g0141a0001c0006t0001g0142a0001c0006t0001g0143others(99): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.313+438C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962531 | ||||||
chr11:65962532
|
A | T | 102 | a0001c0006t0001g0141a0001c0006t0001g0142a0001c0006t0001g0143others(99): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.313+439A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962532 | ||||||
chr11:65962617
|
G | A | 1 | a0001c0004t0002g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+524G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962617 | ||||||
chr11:65962746
|
G | A | 118 | a0001c0005t0001g0007a0001c0005t0001g0012a0001c0005t0001g0022others(115): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.313+653G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962746 | ||||||
chr11:65962767
|
T | C | 5 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+674T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962767 | ||||||
chr11:65962986
|
G | T | 1 | a0001c0004t0002g0070 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.313+893G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962986 | ||||||
chr11:65963105
|
T | C | 1 | a0002c0001t0001g0071 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.314-969T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963105 | ||||||
chr11:65963385
|
G | T | 5 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-689G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963385 | ||||||
chr11:65963444
|
G | A | 5 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-630G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963444 | ||||||
chr11:65963469
|
G | T | 1 | a0001c0003t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.314-605G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963469 | ||||||
chr11:65963474
|
T | G | 154 | a0001c0003t0002g0067a0001c0003t0003g0021a0001c0003t0003g0059others(151): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.314-600T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963474 | ||||||
chr11:65963482
|
G | T | 72 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0034others(69): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.314-592G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963482 | ||||||
chr11:65963483
|
T | G | 2 | a0001c0002t0002g0201a0001c0002t0008g0202 | 2 | HG01496.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.314-591T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963483 | ||||||
chr11:65963544
|
C | T | 1 | a0001c0005t0002g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.314-530C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963544 | ||||||
chr11:65963885
|
G | A | 2 | a0001c0005t0001g0012a0001c0005t0001g0156 | 4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-189G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963885 | ||||||
chr11:65963902
|
C | T | 1 | a0002c0001t0017g0155 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.314-172C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963902 | ||||||
chr11:65964153
|
T | C | 1 | a0002c0001t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.371+22T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964153 | ||||||
chr11:65964387
|
G | T | 2 | a0001c0005t0001g0159a0001c0005t0001g0160 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.372-128G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964387 | ||||||
chr11:65964470
|
C | A | 1 | a0001c0004t0002g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.372-45C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964470 | ||||||
chr11:65964486
|
C | G | 1 | a0002c0001t0001g0154 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.372-29C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964486 | ||||||
chr11:65964598
|
G | T | 1 | a0001c0005t0002g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.427+28G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964598 | ||||||
chr11:65964615
|
T | C | 3 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.427+45T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964615 | ||||||
chr11:65964710
|
C | T | 1 | a0002c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.427+140C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964710 | ||||||
chr11:65964812
|
G | C | 1 | a0001c0007t0002g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.427+242G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964812 | ||||||
chr11:65964843
|
C | T | 1 | a0002c0001t0001g0152 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.428-249C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964843 | ||||||
chr11:65965022
|
G | A | 1 | a0001c0002t0002g0203 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.428-70G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65965022 | ||||||
chr11:65965059
|
G | A | 1 | a0002c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.428-33G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65965059 | ||||||
chr11:65965297
|
G | C | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555-45G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965297 | ||||||
chr11:65965299
|
G | T | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555-43G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965299 | ||||||
chr11:65965319
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.555-23G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965319 | ||||||
chr11:65965329
|
T | C | 160 | a0001c0002t0008g0205a0001c0003t0002g0067a0001c0003t0003g0021others(157): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.555-13T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965329 | ||||||
chr11:65965510
|
C | T | 1 | a0001c0003t0002g0200 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.660+63C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965510 | ||||||
chr11:65965537
|
G | A | 1 | a0001c0002t0002g0206 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.660+90G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965537 | ||||||
chr11:65965629
|
T | C | 1 | a0001c0017t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.661-73T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965629 | ||||||
chr11:65965679
|
G | A | 1 | a0011c0020t0002g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661-23G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965679 | ||||||
chr11:65965818
|
G | A | 138 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(135): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.738+39G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 6/19 | chr11 | 65965818 | ||||||
chr11:65965829
|
G | A | 1 | a0001c0002t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738+50G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 6/19 | chr11 | 65965829 | ||||||
chr11:65965868
|
T | A | 1 | a0002c0001t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.739-19T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 6/19 | chr11 | 65965868 | ||||||
chr11:65965994
|
G | A | 4 | a0002c0001t0001g0075a0002c0001t0001g0076a0002c0001t0001g0077others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01361.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.838+8G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 7/19 | chr11 | 65965994 | ||||||
chr11:65966072
|
C | T | 2 | a0001c0003t0004g0013a0001c0003t0004g0168 | 4 | HG01243.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.839-4C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 7/19 | chr11 | 65966072 | ||||||
chr11:65966667
|
G | A | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1188+111G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966667 | ||||||
chr11:65966762
|
C | G | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1188+206C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966762 | ||||||
chr11:65966838
|
C | T | 2 | a0001c0004t0007g0068a0001c0004t0007g0069 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1188+282C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966838 | ||||||
chr11:65966966
|
C | T | 7 | a0001c0003t0002g0067a0001c0004t0006g0045a0001c0004t0006g0046others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-293C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966966 | ||||||
chr11:65966972
|
G | A | 5 | a0001c0003t0002g0067a0001c0004t0006g0045a0001c0004t0006g0046others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-287G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966972 | ||||||
chr11:65966994
|
G | A | 1 | a0002c0001t0001g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1189-265G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966994 | ||||||
chr11:65967068
|
C | T | 159 | a0001c0003t0002g0067a0001c0003t0002g0162a0001c0003t0002g0163others(156): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1189-191C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65967068 | ||||||
chr11:65967074
|
C | T | 15 | a0001c0003t0002g0014a0001c0003t0002g0189a0001c0003t0002g0190others(12): Show | 16 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-185C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65967074 | ||||||
chr11:65967413
|
T | C | 5 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1313+30T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 10/19 | chr11 | 65967413 | ||||||
chr11:65967912
|
A | C | 1 | a0002c0001t0001g0151 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1572+91A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65967912 | ||||||
chr11:65967949
|
GT | G | 252 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(249): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1572+146delT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65967949 | |||||
chr11:65967988
|
C | T | 1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+167C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65967988 | ||||||
chr11:65968095
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1572+274G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968095 | ||||||
chr11:65968150
|
A | G | 2 | a0002c0001t0001g0077a0002c0001t0001g0078 | 2 | HG00099.hp2 HG00140.hp1 |
intron_variant | MODIFIER | c.1572+329A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968150 | ||||||
chr11:65968201
|
G | A | 102 | a0001c0006t0001g0141a0001c0006t0001g0142a0001c0006t0001g0143others(99): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1572+380G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968201 | ||||||
chr11:65968391
|
T | C | 20 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(17): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+570T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968391 | ||||||
chr11:65968403
|
T | C | 269 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(266): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1572+582T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968403 | ||||||
chr11:65968640
|
C | T | 3 | a0001c0004t0007g0068a0001c0004t0007g0069a0001c0005t0001g0160 | 3 | HG02257.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1572+819C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968640 | ||||||
chr11:65968641
|
G | A | 1 | a0001c0004t0002g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1572+820G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968641 | ||||||
chr11:65968651
|
G | A | 2 | a0001c0007t0002g0017a0001c0007t0002g0048 | 3 | HG01891.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1572+830G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968651 | ||||||
chr11:65968702
|
G | A | 1 | a0001c0003t0005g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1572+881G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968702 | ||||||
chr11:65968737
|
G | T | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+916G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968737 | ||||||
chr11:65968776
|
G | A | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+955G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968776 | ||||||
chr11:65968860
|
G | A | 1 | a0001c0003t0002g0162 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1572+1039G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968860 | ||||||
chr11:65968980
|
T | G | 1 | a0001c0002t0002g0034 | 2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1572+1159T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968980 | ||||||
chr11:65968981
|
C | G | 1 | a0002c0001t0001g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1572+1160C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968981 | ||||||
chr11:65969132
|
C | T | 3 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+1311C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969132 | ||||||
chr11:65969269
|
C | A | 1 | a0002c0001t0001g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1572+1448C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969269 | ||||||
chr11:65969323
|
C | T | 2 | a0001c0002t0003g0255a0001c0002t0003g0256 | 2 | HG02040.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1572+1502C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969323 | ||||||
chr11:65969388
|
A | T | 1 | a0002c0001t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1572+1567A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969388 | ||||||
chr11:65969548
|
C | T | 1 | a0001c0004t0002g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1572+1727C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969548 | ||||||
chr11:65969611
|
C | T | 1 | a0002c0001t0001g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1572+1790C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969611 | ||||||
chr11:65969662
|
G | A | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+1841G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969662 | ||||||
chr11:65969662
|
G | GCCTCCAC others(10): Show |
1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+1842_1572+185 others(21): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65969662 | |||||
chr11:65969755
|
G | T | 1 | a0002c0001t0001g0150 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1572+1934G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969755 | ||||||
chr11:65969846
|
C | T | 8 | a0001c0005t0001g0007a0001c0005t0001g0012a0001c0005t0001g0022others(5): Show | 16 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+2025C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969846 | ||||||
chr11:65969884
|
A | G | 1 | a0001c0003t0004g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1572+2063A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969884 | ||||||
chr11:65970017
|
C | T | 1 | a0001c0002t0002g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1572+2196C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970017 | ||||||
chr11:65970160
|
C | T | 6 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(3): Show | 7 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+2339C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970160 | ||||||
chr11:65970266
|
C | T | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+2445C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970266 | ||||||
chr11:65970321
|
G | A | 1 | a0002c0001t0001g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1572+2500G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970321 | ||||||
chr11:65970344
|
A | C | 36 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(33): Show | 47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+2523A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970344 | ||||||
chr11:65970346
|
T | A | 1 | a0001c0002t0013g0209 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1572+2525T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970346 | ||||||
chr11:65970368
|
A | G | 3 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+2547A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970368 | ||||||
chr11:65970396
|
T | G | 5 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+2575T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970396 | ||||||
chr11:65970428
|
G | A | 20 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(17): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+2607G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970428 | ||||||
chr11:65970444
|
C | T | 7 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(4): Show | 8 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+2623C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970444 | ||||||
chr11:65970470
|
C | T | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+2649C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970470 | ||||||
chr11:65970497
|
A | G | 1 | a0001c0003t0005g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1572+2676A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970497 | ||||||
chr11:65970523
|
G | A | 7 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(4): Show | 8 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+2702G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970523 | ||||||
chr11:65970567
|
GCTGTGGG others(22): Show |
G | 1 | a0001c0002t0002g0203 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1572+2747_1572+277 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970567 | ||||||
chr11:65970624
|
GT | G | 138 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(135): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1572+2808delT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970624 | |||||
chr11:65970663
|
G | A | 15 | a0001c0005t0001g0007a0001c0005t0001g0012a0001c0005t0001g0022others(12): Show | 24 | HG01106.hp1 HG01934.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1572+2842G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970663 | ||||||
chr11:65970667
|
T | C | 248 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(245): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1572+2846T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970667 | ||||||
chr11:65970728
|
A | C | 7 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+2907A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970728 | ||||||
chr11:65970777
|
A | AATTCATG others(84): Show |
4 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(1): Show | 4 | HG01109.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+2975_1572+306 others(95): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970777 | |||||
chr11:65970794
|
G | GGGAGGGG others(83): Show |
1 | a0001c0002t0003g0254 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1572+2995_1572+308 others(94): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970794 | |||||
chr11:65970794
|
GGGAGGGG others(112): Show |
G | 4 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0261others(1): Show | 4 | HG01106.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3085_1572+320 others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970794 | |||||
chr11:65970827
|
G | GGGGGATG others(86): Show |
1 | a0002c0001t0001g0029 | 2 | NA18974.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1572+3030_1572+303 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970827 | |||||
chr11:65970845
|
T | TGAGCTGC others(25): Show |
43 | a0001c0006t0001g0141a0001c0006t0001g0142a0001c0006t0001g0143others(40): Show | 59 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1572+3030_1572+303 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970845 | |||||
chr11:65970847
|
A | AGCT | 55 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(52): Show | 94 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1572+3028_1572+303 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | |||||
chr11:65970847
|
A | AGCTGAGG others(54): Show |
3 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+3059_1572+306 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | |||||
chr11:65970847
|
A | AGCTGCTG others(711): Show |
1 | a0002c0001t0001g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1572+3030_1572+303 others(722): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | |||||
chr11:65970847
|
A | AGCTGCTG others(801): Show |
2 | a0002c0001t0001g0115a0002c0001t0001g0116 | 2 | HG01123.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1572+3030_1572+303 others(812): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | |||||
chr11:65970874
|
T | G | 55 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(52): Show | 94 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1572+3053T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970874 | ||||||
chr11:65970879
|
T | TGAGGAGG others(51): Show |
3 | a0002c0001t0001g0112a0002c0001t0001g0113a0002c0001t0001g0114 | 3 | HG01168.hp1 HG01169.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1572+3059_1572+306 others(62): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | |||||
chr11:65970879
|
T | TGAGGAGG others(80): Show |
50 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(47): Show | 89 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1572+3059_1572+306 others(91): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | |||||
chr11:65970879
|
T | TGAGGAGG others(167): Show |
1 | a0002c0001t0001g0083 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1572+3059_1572+306 others(178): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | |||||
chr11:65970879
|
T | TGAGGAGG others(232): Show |
1 | a0002c0001t0001g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1572+3059_1572+306 others(243): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | |||||
chr11:65970879
|
T | TGCTGAGG others(54): Show |
9 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1572+3084_1572+308 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | |||||
chr11:65970888
|
G | A | 46 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047others(43): Show | 62 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1572+3067G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970888 | ||||||
chr11:65970895
|
G | GGTGGGAT others(25): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3084_1572+308 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970895 | |||||
chr11:65970895
|
G | T | 3 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+3074G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970895 | ||||||
chr11:65970904
|
C | CATG | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3084_1572+308 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970904 | |||||
chr11:65970906
|
G | T | 144 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(141): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1572+3085G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970906 | ||||||
chr11:65970908
|
A | AGCT | 6 | a0001c0003t0003g0065a0001c0016t0002g0066a0002c0001t0001g0082others(3): Show | 6 | HG01123.hp1 HG01257.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3089_1572+309 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970908 | |||||
chr11:65970908
|
A | AGCTGCTG others(57): Show |
1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3091_1572+309 others(68): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970908 | |||||
chr11:65970908
|
A | T | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3087A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970908 | ||||||
chr11:65970911
|
TGAGGAGG others(19): Show |
T | 20 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(17): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+3092_1572+311 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970911 | |||||
chr11:65970917
|
G | A | 2 | a0001c0004t0007g0068a0001c0016t0002g0066 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1572+3096G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970917 | ||||||
chr11:65970922
|
A | G | 3 | a0001c0002t0002g0033a0001c0005t0002g0041a0001c0005t0002g0262 | 5 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3101A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970922 | ||||||
chr11:65970924
|
G | T | 2 | a0001c0004t0007g0068a0001c0016t0002g0066 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1572+3103G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970924 | ||||||
chr11:65970935
|
T | G | 3 | a0001c0002t0002g0033a0001c0005t0002g0041a0001c0005t0002g0262 | 5 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3114T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970935 | ||||||
chr11:65970935
|
T | TGAGCTGA others(86): Show |
4 | a0001c0002t0003g0016a0001c0002t0003g0251a0001c0002t0003g0252others(1): Show | 6 | HG00140.hp2 HG00280.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3149_1572+315 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970935 | |||||
chr11:65970946
|
G | A | 21 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(18): Show | 32 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+3125G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970946 | ||||||
chr11:65970953
|
G | T | 20 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(17): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+3132G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970953 | ||||||
chr11:65970964
|
T | TGAGCTGA others(22): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3171_1572+317 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970964 | |||||
chr11:65970966
|
A | AGCT | 8 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(5): Show | 8 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+3147_1572+314 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | |||||
chr11:65970966
|
A | AGCTGAGG others(25): Show |
1 | a0001c0002t0002g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1572+3176_1572+320 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | |||||
chr11:65970966
|
A | AGCTGAGG others(179): Show |
4 | a0002c0001t0001g0026a0002c0001t0001g0027a0002c0001t0001g0109others(1): Show | 6 | NA18983.hp2 NA19004.hp1 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3178_1572+317 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | |||||
chr11:65970966
|
A | AGCTGAGG others(298): Show |
2 | a0001c0005t0001g0012a0001c0005t0001g0156 | 4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3178_1572+317 others(309): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | |||||
chr11:65970966
|
A | AGCTGCTG others(455): Show |
1 | a0001c0017t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3149_1572+315 others(466): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | |||||
chr11:65970966
|
A | AGCTGCTG others(60): Show |
1 | a0001c0003t0003g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1572+3149_1572+315 others(71): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | |||||
chr11:65970993
|
TGAGCTGC others(57): Show |
T | 1 | a0003c0008t0002g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1572+3179_1572+324 others(68): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970993 | |||||
chr11:65970995
|
AGCT | A | 7 | a0001c0005t0001g0007a0001c0005t0001g0022a0001c0005t0001g0030others(4): Show | 13 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1572+3179_1572+318 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970995 | |||||
chr11:65970995
|
AGCTGCTG others(208): Show |
A | 19 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(16): Show | 30 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1572+3179_1572+339 others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970995 | |||||
chr11:65970998
|
T | TGAGGAGG others(19): Show |
1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3178_1572+317 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970998 | |||||
chr11:65970998
|
T | TGCTGAGG others(458): Show |
1 | a0001c0002t0003g0210 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1572+3207_1572+320 others(469): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970998 | |||||
chr11:65971007
|
G | A | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3186G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971007 | ||||||
chr11:65971014
|
G | T | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3193G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971014 | ||||||
chr11:65971028
|
G | GCTGAGGA others(19): Show |
1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3207_1572+320 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971028 | ||||||
chr11:65971029
|
G | C | 81 | a0001c0002t0002g0031a0001c0002t0002g0033a0001c0002t0003g0016others(78): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1572+3208G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971029 | ||||||
chr11:65971030
|
T | A | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3209T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971030 | ||||||
chr11:65971044
|
G | A | 24 | a0001c0002t0002g0031a0001c0002t0002g0033a0001c0002t0003g0016others(21): Show | 38 | HG00140.hp2 HG00280.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1572+3223G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971044 | ||||||
chr11:65971044
|
G | GTGGTGGG others(89): Show |
2 | a0002c0001t0001g0084a0002c0001t0001g0085 | 2 | HG02015.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1572+3235_1572+323 others(100): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971044 | |||||
chr11:65971056
|
A | G | 4 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3235A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971056 | ||||||
chr11:65971057
|
G | GGAGCTGA others(22): Show |
1 | a0002c0001t0001g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1572+3272_1572+330 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | |||||
chr11:65971057
|
G | GGAGCTGA others(80): Show |
1 | a0001c0003t0002g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1572+3277_1572+327 others(91): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | |||||
chr11:65971057
|
G | GGAGCTGA others(420): Show |
2 | a0001c0003t0002g0162a0001c0003t0002g0164 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1572+3277_1572+327 others(431): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | |||||
chr11:65971057
|
G | GGAGCTGA others(51): Show |
1 | a0001c0017t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3280_1572+328 others(62): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | |||||
chr11:65971057
|
G | T | 75 | a0001c0002t0002g0031a0001c0002t0002g0033a0001c0002t0003g0016others(72): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1572+3236G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971057 | ||||||
chr11:65971058
|
G | A | 2 | a0002c0001t0001g0084a0002c0001t0001g0085 | 2 | HG02015.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1572+3237G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971058 | ||||||
chr11:65971059
|
A | AGCT | 66 | a0001c0002t0002g0033a0001c0002t0003g0016a0001c0002t0003g0251others(63): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1572+3240_1572+324 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | |||||
chr11:65971059
|
A | AGCTGAGG others(618): Show |
3 | a0002c0001t0001g0137a0002c0001t0001g0138a0002c0001t0001g0139 | 3 | HG00621.hp1 NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(629): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | |||||
chr11:65971059
|
A | AGCTGCTG others(179): Show |
1 | a0001c0002t0002g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1572+3242_1572+324 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | |||||
chr11:65971059
|
A | AGCTGCTG others(243): Show |
1 | a0001c0002t0003g0255 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1572+3242_1572+324 others(254): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | |||||
chr11:65971059
|
A | T | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3238A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971059 | ||||||
chr11:65971068
|
G | GGGGGATG others(25): Show |
6 | a0001c0005t0001g0007a0001c0005t0001g0022a0001c0005t0001g0030others(3): Show | 12 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1572+3271_1572+327 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971068 | |||||
chr11:65971073
|
A | ATGGTGGG others(391): Show |
1 | a0001c0003t0002g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1572+3277_1572+327 others(402): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971073 | |||||
chr11:65971073
|
A | G | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3252A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971073 | ||||||
chr11:65971073
|
ATGG | A | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3256_1572+325 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971073 | |||||
chr11:65971085
|
A | G | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3264A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971085 | ||||||
chr11:65971086
|
T | G | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3265T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971086 | ||||||
chr11:65971088
|
A | AGCT | 67 | a0001c0002t0002g0033a0001c0002t0003g0016a0001c0002t0003g0251others(64): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1572+3269_1572+327 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGAGG others(301): Show |
1 | a0002c0001t0001g0117 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(312): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGAGG others(182): Show |
1 | a0002c0001t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(193): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGAGG others(182): Show |
6 | a0002c0001t0001g0028a0002c0001t0001g0124a0002c0001t0001g0125others(3): Show | 7 | HG02074.hp1 HG02132.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(193): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGAGG others(400): Show |
1 | a0002c0001t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(411): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGAGG others(461): Show |
3 | a0002c0001t0001g0011a0002c0001t0001g0135a0002c0001t0001g0136 | 4 | HG00609.hp2 NA18980.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(472): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGCTG others(28): Show |
1 | a0001c0005t0001g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1572+3271_1572+327 others(39): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971088
|
A | AGCTGCTG others(60): Show |
2 | a0001c0005t0001g0012a0001c0005t0001g0156 | 4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3271_1572+327 others(71): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | |||||
chr11:65971113
|
CATG | C | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3294_1572+329 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971113 | |||||
chr11:65971119
|
C | A | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3298C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971119 | ||||||
chr11:65971120
|
T | A | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3299T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971120 | ||||||
chr11:65971120
|
T | TGAGGAGG others(891): Show |
1 | a0002c0001t0001g0119 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(902): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | |||||
chr11:65971120
|
T | TGAGGAGG others(641): Show |
1 | a0002c0001t0001g0121 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(652): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | |||||
chr11:65971120
|
T | TGAGGAGG others(614): Show |
1 | a0002c0001t0001g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(625): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | |||||
chr11:65971120
|
T | TGAGGAGG others(615): Show |
17 | a0002c0001t0001g0003a0002c0001t0001g0011a0002c0001t0001g0074others(14): Show | 28 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(626): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | |||||
chr11:65971120
|
T | TGAGGAGG others(647): Show |
1 | a0002c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(658): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | |||||
chr11:65971120
|
TGCTGAGG others(51): Show |
T | 3 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0263 | 3 | HG01106.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1572+3317_1572+337 others(62): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | |||||
chr11:65971134
|
A | ATGG | 206 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(203): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1572+3314_1572+331 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | |||||
chr11:65971134
|
A | ATGGTGGG others(307): Show |
1 | a0001c0002t0003g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1572+3316_1572+331 others(318): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | |||||
chr11:65971134
|
A | ATGGTGGG others(490): Show |
2 | a0001c0002t0003g0249a0001c0002t0003g0250 | 2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1572+3316_1572+331 others(501): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | |||||
chr11:65971134
|
A | ATGGTGGG others(679): Show |
2 | a0001c0002t0002g0035a0001c0002t0002g0231 | 3 | HG02559.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1572+3316_1572+331 others(690): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | |||||
chr11:65971134
|
A | G | 1 | a0001c0002t0009g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1572+3313A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971134 | ||||||
chr11:65971144
|
T | G | 1 | a0001c0002t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572+3323T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971144 | ||||||
chr11:65971146
|
AGCT | A | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3330_1572+333 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971146 | |||||
chr11:65971149
|
T | TGAGGAGG others(1010): Show |
1 | a0001c0002t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572+3329_1572+333 others(1021): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971149 | |||||
chr11:65971149
|
TGCTGAGG others(22): Show |
T | 1 | a0001c0005t0002g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3355_1572+338 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971149 | |||||
chr11:65971174
|
C | CATG | 56 | a0001c0002t0002g0035a0001c0002t0002g0207a0001c0002t0002g0231others(53): Show | 73 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1572+3354_1572+335 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | |||||
chr11:65971174
|
C | CATGAGCT others(336): Show |
1 | a0001c0003t0002g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1572+3354_1572+335 others(347): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | |||||
chr11:65971174
|
C | CATGAGCT others(592): Show |
1 | a0002c0001t0001g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1572+3354_1572+335 others(603): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | |||||
chr11:65971174
|
C | CATGAGCT others(589): Show |
2 | a0001c0006t0001g0142a0001c0006t0001g0143 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1572+3354_1572+335 others(600): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | |||||
chr11:65971175
|
A | AT | 72 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(69): Show | 99 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1572+3354_1572+335 others(5): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971175 | ||||||
chr11:65971176
|
G | GGAGCTGA others(22): Show |
1 | a0001c0005t0001g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1572+3355_1572+335 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971176 | ||||||
chr11:65971176
|
G | T | 8 | a0001c0002t0003g0211a0001c0005t0001g0007a0001c0005t0001g0022others(5): Show | 14 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1572+3355G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971176 | ||||||
chr11:65971176
|
GAAGCTGA others(22): Show |
G | 1 | a0003c0008t0002g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+338 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971176 | ||||||
chr11:65971177
|
A | AAGCTGAG others(949): Show |
1 | a0011c0020t0002g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1572+3383_1572+338 others(960): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(22): Show |
32 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(29): Show | 47 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+3362_1572+339 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(4080): Show |
1 | a0001c0003t0002g0258 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(4091): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(2857): Show |
1 | a0001c0003t0002g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(2868): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(2921): Show |
2 | a0001c0003t0002g0190a0001c0003t0002g0200 | 2 | HG00597.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(2932): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(2922): Show |
1 | a0001c0003t0002g0191 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(2933): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1553): Show |
1 | a0001c0003t0002g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1564): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(2407): Show |
4 | a0001c0003t0002g0014a0001c0003t0002g0176a0001c0003t0002g0199others(1): Show | 5 | HG02056.hp2 NA18947.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(2418): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1524): Show |
2 | a0001c0003t0002g0195a0001c0003t0002g0196 | 2 | NA18955.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(1535): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1495): Show |
1 | a0001c0003t0002g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1506): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(3357): Show |
1 | a0001c0003t0002g0198 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(3368): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(2081): Show |
1 | a0001c0003t0004g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(2092): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1525): Show |
1 | a0001c0003t0010g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1536): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1798): Show |
1 | a0001c0003t0005g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1809): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1557): Show |
2 | a0001c0003t0005g0183a0001c0003t0005g0185 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(1568): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1711): Show |
1 | a0001c0003t0005g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1722): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1557): Show |
2 | a0001c0003t0004g0013a0001c0003t0004g0168 | 4 | HG01243.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(1568): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(673): Show |
1 | a0001c0002t0003g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(684): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1980): Show |
1 | a0001c0003t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1991): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(2407): Show |
2 | a0001c0003t0002g0180a0009c0018t0002g0179 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(2418): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(1274): Show |
1 | a0001c0002t0002g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1285): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AAGCTGAG others(644): Show |
4 | a0001c0002t0003g0016a0001c0002t0003g0252a0001c0002t0003g0253others(1): Show | 6 | HG00140.hp2 HG00280.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(655): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | |||||
chr11:65971177
|
A | AGCTGCTG others(1334): Show |
1 | a0001c0002t0002g0031 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1345): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(53): Show |
1 | a0002c0001t0001g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(64): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1316): Show |
1 | a0001c0003t0004g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1327): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(736): Show |
1 | a0001c0002t0002g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(951): Show |
1 | a0001c0002t0003g0032 | 2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(962): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(736): Show |
1 | a0001c0003t0002g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(736): Show |
1 | a0001c0002t0002g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1410): Show |
2 | a0001c0002t0003g0212a0001c0002t0003g0213 | 2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1421): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(85): Show |
1 | a0001c0003t0003g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(96): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(736): Show |
1 | a0001c0002t0008g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(768): Show |
1 | a0001c0002t0003g0171 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(779): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(765): Show |
1 | a0001c0002t0002g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(776): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1230): Show |
1 | a0001c0002t0008g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1241): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(704): Show |
4 | a0001c0002t0002g0204a0001c0002t0002g0219a0001c0002t0002g0220others(1): Show | 4 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(715): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1427): Show |
4 | a0001c0002t0002g0203a0001c0002t0002g0215a0001c0002t0002g0216others(1): Show | 4 | HG00558.hp2 HG02027.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1438): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1305): Show |
2 | a0001c0002t0002g0217a0001c0002t0002g0218 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1316): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1398): Show |
14 | a0001c0002t0002g0008a0001c0002t0002g0010a0001c0002t0002g0034others(11): Show | 20 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1409): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1398): Show |
1 | a0001c0002t0002g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1409): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(829): Show |
1 | a0001c0002t0003g0229 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(840): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(768): Show |
20 | a0001c0002t0001g0036a0001c0002t0002g0038a0001c0002t0002g0174others(17): Show | 37 | HG01123.hp2 HG01169.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(779): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(925): Show |
1 | a0001c0002t0003g0239 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(936): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(769): Show |
1 | a0005c0010t0003g0242 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(780): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1366): Show |
1 | a0001c0002t0002g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1377): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1395): Show |
1 | a0001c0002t0002g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1406): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(800): Show |
2 | a0001c0002t0003g0187a0001c0002t0003g0244 | 2 | HG02293.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(811): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(364): Show |
1 | a0001c0002t0002g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(375): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(864): Show |
1 | a0001c0002t0009g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(875): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(646): Show |
1 | a0001c0002t0003g0245 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(657): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGCTGCTG others(1552): Show |
1 | a0001c0002t0002g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1563): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | AGGTGCTG others(518): Show |
2 | a0001c0002t0003g0015a0001c0002t0003g0247 | 4 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(529): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | C | 60 | a0001c0002t0002g0035a0001c0002t0002g0207a0001c0002t0002g0231others(57): Show | 77 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1572+3356A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971177
|
A | G | 13 | a0001c0002t0003g0211a0001c0003t0002g0162a0001c0003t0002g0164others(10): Show | 19 | HG00099.hp2 HG01109.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1572+3356A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | ||||||
chr11:65971178
|
A | AGCTGAGG others(54): Show |
29 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(26): Show | 48 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971178 | |||||
chr11:65971178
|
A | AGCTGAGG others(86): Show |
2 | a0001c0003t0004g0167a0001c0003t0004g0259 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971178 | |||||
chr11:65971178
|
A | AGCTGAGG others(179): Show |
2 | a0002c0001t0001g0115a0002c0001t0001g0116 | 2 | HG01123.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971178 | |||||
chr11:65971178
|
A | T | 60 | a0001c0002t0002g0035a0001c0002t0002g0207a0001c0002t0002g0231others(57): Show | 77 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1572+3357A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971178 | ||||||
chr11:65971192
|
A | G | 1 | a0001c0006t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1572+3371A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971192 | ||||||
chr11:65971195
|
G | GTGGGATT others(83): Show |
2 | a0001c0005t0001g0012a0001c0005t0001g0156 | 4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(94): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | |||||
chr11:65971195
|
G | GTGGGATT others(147): Show |
4 | a0002c0001t0001g0082a0002c0001t0001g0117a0002c0001t0001g0118others(1): Show | 4 | HG00673.hp2 HG01257.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(158): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | |||||
chr11:65971195
|
G | GTGGGATT others(272): Show |
6 | a0001c0005t0001g0007a0001c0005t0001g0022a0001c0005t0001g0030others(3): Show | 12 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(283): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | |||||
chr11:65971195
|
G | GTGGGATT others(22): Show |
6 | a0002c0001t0001g0026a0002c0001t0001g0027a0002c0001t0001g0084others(3): Show | 8 | HG02015.hp1 HG03704.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+3378_1572+340 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | |||||
chr11:65971205
|
T | G | 27 | a0001c0006t0001g0142a0001c0006t0001g0143a0002c0001t0001g0003others(24): Show | 38 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1572+3384T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971205 | ||||||
chr11:65971205
|
T | TGAGCTGA others(804): Show |
1 | a0002c0001t0001g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(815): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971205 | |||||
chr11:65971207
|
AGCT | A | 3 | a0001c0002t0002g0033a0002c0001t0001g0081a0002c0001t0001g0105 | 3 | HG01978.hp1 HG06807.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1572+3391_1572+339 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971207 | |||||
chr11:65971210
|
T | TGAGGAGG others(455): Show |
1 | a0001c0002t0003g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(466): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | |||||
chr11:65971210
|
T | TGAGGAGG others(1878): Show |
1 | a0001c0003t0002g0193 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1889): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | |||||
chr11:65971210
|
T | TGAGGAGG others(1422): Show |
1 | a0001c0003t0002g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1433): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | |||||
chr11:65971210
|
T | TGAGGAGG others(208): Show |
1 | a0002c0001t0001g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(219): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | |||||
chr11:65971210
|
T | TGAGGAGG others(144): Show |
3 | a0001c0003t0002g0162a0001c0003t0002g0164a0001c0003t0002g0165 | 3 | HG01109.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(155): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | |||||
chr11:65971224
|
A | G | 3 | a0001c0003t0002g0162a0001c0003t0002g0164a0001c0003t0002g0165 | 3 | HG01109.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1572+3403A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971224 | ||||||
chr11:65971237
|
T | G | 24 | a0001c0003t0002g0163a0001c0003t0003g0021a0001c0003t0003g0060others(21): Show | 32 | HG01243.hp2 HG01934.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1572+3416T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971237 | ||||||
chr11:65971238
|
G | A | 10 | a0001c0003t0004g0167a0001c0003t0004g0259a0001c0005t0001g0007others(7): Show | 18 | HG01934.hp1 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1572+3417G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971238 | ||||||
chr11:65971239
|
A | AGCT | 78 | a0001c0002t0003g0249a0001c0002t0003g0250a0001c0005t0001g0160others(75): Show | 122 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1572+3420_1572+342 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971239 | |||||
chr11:65971239
|
A | AGCTGCTG others(769): Show |
3 | a0001c0002t0002g0207a0001c0002t0002g0240a0001c0002t0002g0241 | 3 | HG02647.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1572+3422_1572+342 others(780): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971239 | |||||
chr11:65971242
|
TGAGGAGG others(19): Show |
T | 3 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0263 | 3 | HG01106.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1572+3423_1572+344 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971242 | |||||
chr11:65971253
|
A | G | 1 | a0001c0017t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3432A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971253 | ||||||
chr11:65971266
|
T | G | 1 | a0001c0005t0002g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3445T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971266 | ||||||
chr11:65971267
|
G | A | 1 | a0001c0005t0002g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3446G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971267 | ||||||
chr11:65971268
|
A | AGCT | 85 | a0001c0002t0002g0033a0001c0003t0003g0059a0001c0004t0002g0004others(82): Show | 125 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1572+3449_1572+345 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | |||||
chr11:65971268
|
A | AGCTGAGG others(89): Show |
10 | a0001c0003t0003g0021a0001c0003t0003g0060a0001c0003t0003g0061others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1572+3505_1572+350 others(100): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | |||||
chr11:65971268
|
A | AGCTGAGG others(243): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(254): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | |||||
chr11:65971268
|
A | AGCTGCTG others(153): Show |
3 | a0002c0001t0001g0005a0002c0001t0001g0087a0008c0013t0001g0089 | 7 | HG00423.hp1 HG00544.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+3451_1572+345 others(164): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | |||||
chr11:65971268
|
A | AGCTGCTG others(153): Show |
14 | a0002c0001t0001g0001a0002c0001t0001g0006a0002c0001t0001g0009others(11): Show | 20 | HG00738.hp2 HG01257.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1572+3451_1572+345 others(164): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | |||||
chr11:65971268
|
AGCTGAGG others(57): Show |
A | 1 | a0001c0005t0002g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3481_1572+354 others(68): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | |||||
chr11:65971275
|
G | T | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3454G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971275 | ||||||
chr11:65971282
|
ATGG | A | 32 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0263others(29): Show | 51 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1572+3465_1572+346 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971282 | |||||
chr11:65971300
|
T | TGAGGAGG others(19): Show |
1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3480_1572+348 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971300 | |||||
chr11:65971314
|
ATGG | A | 17 | a0002c0001t0001g0001a0002c0001t0001g0009a0002c0001t0001g0024others(14): Show | 20 | HG00099.hp1 HG00438.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1572+3497_1572+349 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971314 | |||||
chr11:65971317
|
G | GTGGGATT others(22): Show |
1 | a0002c0001t0001g0105 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971317 | |||||
chr11:65971327
|
G | GAAGCTGA others(208): Show |
1 | a0001c0006t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1572+3506_1572+350 others(219): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | ||||||
chr11:65971327
|
G | T | 134 | a0001c0002t0002g0033a0001c0003t0002g0162a0001c0003t0002g0163others(131): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1572+3506G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | ||||||
chr11:65971327
|
G | TGAGCTGC others(1898): Show |
1 | a0001c0003t0004g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(1909): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | ||||||
chr11:65971327
|
G | TGAGCTGC others(1403): Show |
1 | a0001c0003t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(1414): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | ||||||
chr11:65971328
|
G | A | 3 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0263 | 3 | HG01106.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1572+3507G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971328 | ||||||
chr11:65971329
|
AGCT | A | 24 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(21): Show | 35 | HG00423.hp1 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572+3513_1572+351 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971329 | |||||
chr11:65971332
|
T | TGCTGAGG others(647): Show |
1 | a0002c0001t0001g0011 | 2 | NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1572+3537_1572+353 others(658): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
T | TGCTGAGG others(461): Show |
1 | a0002c0001t0001g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1572+3537_1572+353 others(472): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
T | TGCTGAGG others(22): Show |
10 | a0002c0001t0001g0026a0002c0001t0001g0027a0002c0001t0001g0081others(7): Show | 11 | HG00597.hp2 HG00738.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1572+3545_1572+357 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
T | TGCTGAGG others(118): Show |
2 | a0002c0001t0001g0005a0002c0001t0001g0088 | 2 | HG02083.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1572+3544_1572+354 others(129): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
T | TGCTGAGG others(86): Show |
1 | a0002c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1572+3544_1572+354 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
T | TGCTGAGG others(118): Show |
8 | a0001c0006t0001g0141a0002c0001t0001g0001a0002c0001t0001g0023others(5): Show | 15 | HG00609.hp1 HG00639.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1572+3544_1572+354 others(129): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
TGCTGAGG others(22): Show |
T | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3545_1572+357 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971332
|
TGCTGAGG others(147): Show |
T | 1 | a0003c0008t0002g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1572+3574_1572+372 others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | |||||
chr11:65971346
|
A | G | 29 | a0001c0006t0001g0142a0001c0006t0001g0143a0002c0001t0001g0003others(26): Show | 40 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1572+3525A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971346 | ||||||
chr11:65971359
|
T | G | 1 | a0001c0003t0003g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1572+3538T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971359 | ||||||
chr11:65971361
|
A | AGCT | 83 | a0001c0002t0002g0033a0001c0003t0002g0162a0001c0003t0002g0163others(80): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1572+3542_1572+354 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971361 | |||||
chr11:65971368
|
G | A | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+3547G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971368 | ||||||
chr11:65971369
|
A | G | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+3548A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971369 | ||||||
chr11:65971370
|
G | A | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+3549G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971370 | ||||||
chr11:65971375
|
A | G | 5 | a0001c0003t0004g0013a0001c0003t0004g0166a0001c0003t0004g0167others(2): Show | 7 | HG01243.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+3554A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971375 | ||||||
chr11:65971388
|
T | G | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3567T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971388 | ||||||
chr11:65971388
|
T | TGAGCTGA others(144): Show |
1 | a0001c0002t0003g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1572+3573_1572+357 others(155): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971388 | |||||
chr11:65971390
|
AGCT | A | 10 | a0001c0003t0003g0065a0001c0005t0001g0007a0001c0005t0001g0012others(7): Show | 18 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1572+3574_1572+357 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971390 | |||||
chr11:65971393
|
T | TGAGGAGG others(173): Show |
1 | a0001c0002t0003g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3573_1572+357 others(184): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGAGGAGG others(115): Show |
5 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+3573_1572+357 others(126): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(22): Show |
1 | a0001c0002t0003g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1572+3577_1572+360 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(963): Show |
2 | a0001c0002t0002g0219a0001c0002t0002g0220 | 2 | HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1572+3605_1572+360 others(974): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(960): Show |
1 | a0001c0002t0002g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1572+3605_1572+360 others(971): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(960): Show |
1 | a0001c0002t0002g0227 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1572+3605_1572+360 others(971): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(266): Show |
1 | a0001c0002t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(277): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(266): Show |
1 | a0001c0002t0002g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(277): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(266): Show |
74 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(71): Show | 104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(277): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971393
|
T | TGCTGAGG others(1358): Show |
1 | a0001c0002t0002g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(1369): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | |||||
chr11:65971425
|
T | TGAGGAGG others(19): Show |
1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3605_1572+360 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | |||||
chr11:65971425
|
T | TGAGGAGG others(388): Show |
4 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(1): Show | 4 | HG01109.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3605_1572+360 others(399): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | |||||
chr11:65971425
|
T | TGCTGAGG others(205): Show |
1 | a0001c0017t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3621_1572+362 others(216): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | |||||
chr11:65971425
|
T | TGCTGAGG others(234): Show |
2 | a0001c0002t0002g0170a0001c0002t0011g0226 | 2 | HG01099.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(245): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | |||||
chr11:65971452
|
T | G | 44 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0261others(41): Show | 66 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1572+3631T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971452 | ||||||
chr11:65971452
|
T | TGAGCTGA others(115): Show |
1 | a0002c0001t0001g0083 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(126): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971452 | |||||
chr11:65971457
|
T | TGAGGAGG others(234): Show |
1 | a0002c0001t0001g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(245): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGAGGAGG others(144): Show |
18 | a0002c0001t0001g0001a0002c0001t0001g0006a0002c0001t0001g0009others(15): Show | 28 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(155): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGAGGAGG others(115): Show |
2 | a0002c0001t0001g0072a0002c0001t0001g0106 | 2 | NA18954.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(126): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(519): Show |
1 | a0002c0001t0001g0011 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(530): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(517): Show |
1 | a0002c0001t0001g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(528): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(1019): Show |
1 | a0002c0001t0001g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(1030): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(426): Show |
1 | a0002c0001t0001g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(437): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(519): Show |
13 | a0001c0006t0001g0143a0002c0001t0001g0003a0002c0001t0001g0075others(10): Show | 19 | HG00099.hp2 HG01070.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1572+3662_1572+366 others(530): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(54): Show |
1 | a0002c0001t0001g0027 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
T | TGCTGAGG others(22): Show |
1 | a0001c0002t0002g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1572+3728_1572+375 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971457
|
TGCTGAGG others(22): Show |
T | 19 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(16): Show | 30 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1572+3728_1572+375 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | |||||
chr11:65971471
|
A | G | 1 | a0002c0001t0001g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1572+3650A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971471 | ||||||
chr11:65971484
|
T | G | 27 | a0001c0004t0007g0069a0001c0005t0001g0007a0001c0005t0001g0012others(24): Show | 40 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1572+3663T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971484 | ||||||
chr11:65971485
|
G | A | 12 | a0001c0006t0001g0142a0002c0001t0001g0003a0002c0001t0001g0074others(9): Show | 16 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3664G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971485 | ||||||
chr11:65971486
|
A | AGCT | 20 | a0001c0002t0002g0170a0001c0002t0011g0226a0001c0003t0002g0162others(17): Show | 21 | HG00673.hp2 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1572+3667_1572+366 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | |||||
chr11:65971486
|
A | AGCTGCTG others(60): Show |
8 | a0001c0005t0001g0007a0001c0005t0001g0012a0001c0005t0001g0022others(5): Show | 16 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3669_1572+367 others(71): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | |||||
chr11:65971486
|
A | AGCTGCTG others(371): Show |
6 | a0001c0003t0003g0021a0001c0003t0003g0060a0001c0003t0003g0061others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1572+3669_1572+367 others(382): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | |||||
chr11:65971486
|
A | AGCTGCTG others(403): Show |
1 | a0001c0003t0003g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1572+3669_1572+367 others(414): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | |||||
chr11:65971486
|
A | AGCTGCTG others(563): Show |
1 | a0001c0003t0003g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1572+3669_1572+367 others(574): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | |||||
chr11:65971513
|
T | G | 36 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(33): Show | 47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+3692T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971513 | ||||||
chr11:65971513
|
T | TGAGCTGA others(949): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3727_1572+372 others(960): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971513 | |||||
chr11:65971515
|
A | AGCT | 42 | a0001c0003t0002g0193a0001c0003t0002g0194a0001c0006t0001g0143others(39): Show | 58 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1572+3696_1572+369 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971515 | |||||
chr11:65971515
|
A | AGCTGAGG others(25): Show |
4 | a0002c0001t0001g0085a0002c0001t0001g0104a0002c0001t0001g0115others(1): Show | 4 | HG01123.hp1 HG02015.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3696_1572+372 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971515 | |||||
chr11:65971515
|
A | AGCTGAGG others(179): Show |
11 | a0002c0001t0001g0001a0002c0001t0001g0009a0002c0001t0001g0024others(8): Show | 13 | HG00099.hp1 HG00438.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1572+3727_1572+372 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971515 | |||||
chr11:65971529
|
ATGG | A | 8 | a0001c0005t0001g0007a0001c0005t0001g0012a0001c0005t0001g0022others(5): Show | 16 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3712_1572+371 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971529 | |||||
chr11:65971542
|
T | G | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3721T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971542 | ||||||
chr11:65971544
|
A | AGCT | 60 | a0001c0003t0002g0193a0001c0003t0002g0194a0001c0005t0002g0042others(57): Show | 87 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1572+3725_1572+372 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971544 | |||||
chr11:65971550
|
GGAGGGGG others(25): Show |
G | 4 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0261others(1): Show | 4 | HG01106.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3750_1572+378 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971550 | |||||
chr11:65971552
|
A | G | 1 | a0002c0001t0001g0105 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1572+3731A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971552 | ||||||
chr11:65971571
|
T | G | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3750T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971571 | ||||||
chr11:65971571
|
T | TGAGCTGC others(25): Show |
1 | a0001c0002t0003g0040 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971571 | |||||
chr11:65971573
|
AGCT | A | 49 | a0001c0005t0002g0264a0001c0006t0001g0143a0002c0001t0001g0001others(46): Show | 71 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1572+3757_1572+375 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971573 | |||||
chr11:65971576
|
T | TGAGGAGG others(19): Show |
34 | a0001c0006t0001g0141a0002c0001t0001g0001a0002c0001t0001g0005others(31): Show | 56 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1572+3756_1572+375 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | |||||
chr11:65971576
|
T | TGAGGAGG others(1074): Show |
1 | a0002c0001t0001g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1572+3756_1572+375 others(1085): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | |||||
chr11:65971576
|
T | TGCTGAGG others(173): Show |
2 | a0002c0001t0001g0086a0002c0001t0001g0105 | 2 | HG00597.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(184): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | |||||
chr11:65971576
|
T | TGCTGAGG others(920): Show |
1 | a0002c0001t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1572+3760_1572+376 others(931): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | |||||
chr11:65971576
|
T | TGCTGAGG others(516): Show |
12 | a0001c0006t0001g0142a0002c0001t0001g0003a0002c0001t0001g0074others(9): Show | 16 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(527): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | |||||
chr11:65971576
|
T | TGCTGAGG others(798): Show |
3 | a0002c0001t0001g0117a0002c0001t0001g0118a0002c0001t0001g0151 | 3 | HG00673.hp2 HG02056.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(809): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | |||||
chr11:65971582
|
A | G | 265 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(262): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1572+3761A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971582 | ||||||
chr11:65971595
|
G | A | 1 | a0001c0004t0014g0053 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1572+3774G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971595 | ||||||
chr11:65971603
|
G | T | 2 | a0001c0003t0002g0193a0001c0003t0002g0194 | 2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1572+3782G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971603 | ||||||
chr11:65971635
|
G | T | 7 | a0001c0003t0002g0193a0001c0003t0002g0194a0002c0001t0001g0028others(4): Show | 8 | HG02074.hp1 HG02132.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+3814G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971635 | ||||||
chr11:65971637
|
A | AGCTGAGG others(452): Show |
2 | a0001c0003t0002g0193a0001c0003t0002g0194 | 2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1572+3840_1572+384 others(463): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971637 | |||||
chr11:65971637
|
A | AGCTGAGG others(182): Show |
5 | a0002c0001t0001g0028a0002c0001t0001g0124a0002c0001t0001g0125others(2): Show | 6 | HG02074.hp1 HG02132.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3840_1572+384 others(193): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971637 | |||||
chr11:65971678
|
G | A | 1 | a0001c0003t0003g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1572+3857G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971678 | ||||||
chr11:65971876
|
A | G | 1 | a0001c0002t0002g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1572+4055A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971876 | ||||||
chr11:65971887
|
A | G | 36 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(33): Show | 47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+4066A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971887 | ||||||
chr11:65971910
|
G | C | 36 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(33): Show | 47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+4089G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971910 | ||||||
chr11:65972078
|
T | G | 158 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(155): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1572+4257T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972078 | ||||||
chr11:65972464
|
T | C | 1 | a0001c0004t0002g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1573-3931T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972464 | ||||||
chr11:65972586
|
T | C | 35 | a0001c0003t0003g0021a0001c0003t0003g0059a0001c0003t0003g0060others(32): Show | 46 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.1573-3809T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972586 | ||||||
chr11:65972661
|
G | A | 1 | a0002c0001t0016g0091 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1573-3734G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972661 | ||||||
chr11:65972785
|
C | CA | 7 | a0001c0002t0002g0222a0001c0002t0002g0257a0001c0002t0003g0187others(4): Show | 7 | HG00597.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573-3595dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65972785 | |||||
chr11:65972801
|
C | A | 1 | a0001c0003t0002g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1573-3594C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972801 | ||||||
chr11:65972844
|
C | T | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1573-3551C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972844 | ||||||
chr11:65972863
|
G | A | 243 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(240): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1573-3532G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972863 | ||||||
chr11:65972873
|
A | G | 1 | a0001c0004t0002g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1573-3522A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972873 | ||||||
chr11:65972893
|
C | T | 1 | a0001c0003t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1573-3502C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972893 | ||||||
chr11:65972897
|
C | T | 1 | a0002c0001t0001g0025 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1573-3498C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972897 | ||||||
chr11:65972899
|
C | T | 111 | a0001c0002t0002g0031a0001c0005t0001g0007a0001c0005t0001g0012others(108): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1573-3496C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972899 | ||||||
chr11:65972900
|
G | C | 1 | a0001c0004t0002g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1573-3495G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972900 | ||||||
chr11:65972901
|
A | G | 9 | a0001c0002t0002g0031a0001c0002t0002g0170a0001c0002t0003g0039others(6): Show | 12 | HG01069.hp2 HG01071.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1573-3494A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972901 | ||||||
chr11:65972905
|
C | T | 1 | a0001c0004t0006g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1573-3490C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972905 | ||||||
chr11:65972909
|
C | T | 3 | a0001c0004t0007g0068a0001c0004t0007g0069a0001c0005t0001g0160 | 3 | HG02257.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1573-3486C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972909 | ||||||
chr11:65972943
|
G | A | 2 | a0001c0004t0006g0045a0001c0004t0006g0046 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1573-3452G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972943 | ||||||
chr11:65972946
|
C | A | 1 | a0001c0002t0003g0232 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1573-3449C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972946 | ||||||
chr11:65972969
|
G | A | 1 | a0002c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1573-3426G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972969 | ||||||
chr11:65972997
|
T | C | 42 | a0001c0002t0001g0036a0001c0002t0002g0233a0001c0002t0003g0002others(39): Show | 64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1573-3398T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972997 | ||||||
chr11:65973099
|
A | G | 1 | a0001c0005t0002g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1573-3296A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973099 | ||||||
chr11:65973131
|
A | G | 272 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(269): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1573-3264A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973131 | ||||||
chr11:65973148
|
T | A | 1 | a0001c0003t0003g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1573-3247T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973148 | ||||||
chr11:65973173
|
C | CA | 4 | a0001c0002t0003g0187a0001c0003t0002g0195a0002c0001t0001g0026others(1): Show | 5 | HG02293.hp1 NA18955.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1573-3213dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65973173 | |||||
chr11:65973391
|
A | G | 2 | a0001c0003t0002g0193a0001c0003t0002g0194 | 2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1573-3004A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973391 | ||||||
chr11:65973463
|
A | G | 1 | a0002c0001t0001g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1573-2932A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973463 | ||||||
chr11:65973520
|
C | T | 6 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(3): Show | 7 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573-2875C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973520 | ||||||
chr11:65973615
|
G | A | 43 | a0001c0002t0002g0008a0001c0002t0002g0010a0001c0002t0002g0031others(40): Show | 52 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1573-2780G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973615 | ||||||
chr11:65973690
|
C | T | 1 | a0002c0001t0017g0155 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1573-2705C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973690 | ||||||
chr11:65974091
|
G | A | 1 | a0001c0002t0002g0223 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1573-2304G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974091 | ||||||
chr11:65974159
|
G | A | 2 | a0001c0002t0002g0219a0001c0002t0002g0220 | 2 | HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1573-2236G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974159 | ||||||
chr11:65974198
|
T | TA | 51 | a0001c0002t0002g0008a0001c0002t0002g0010a0001c0002t0002g0031others(48): Show | 63 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1573-2171dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974198 | |||||
chr11:65974198
|
TA | T | 139 | a0001c0002t0001g0036a0001c0002t0003g0002a0001c0002t0003g0015others(136): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1573-2171delA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974198 | |||||
chr11:65974198
|
TAA | T | 19 | a0001c0002t0003g0253a0001c0003t0002g0178a0001c0004t0002g0004others(16): Show | 30 | HG00673.hp1 HG01099.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1573-2172_1573-217 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974198 | |||||
chr11:65974225
|
T | G | 1 | a0002c0001t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1573-2170T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974225 | ||||||
chr11:65974299
|
G | A | 111 | a0001c0002t0001g0036a0001c0005t0001g0007a0001c0005t0001g0012others(108): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1573-2096G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974299 | ||||||
chr11:65974346
|
C | T | 2 | a0002c0001t0001g0099a0002c0001t0001g0100 | 2 | NA18944.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1573-2049C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974346 | ||||||
chr11:65974371
|
C | CA | 51 | a0001c0002t0002g0215a0001c0002t0002g0219a0001c0002t0002g0224others(48): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1573-2004dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | |||||
chr11:65974371
|
C | CAA | 98 | a0001c0002t0001g0036a0001c0002t0002g0233a0001c0002t0003g0187others(95): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1573-2005_1573-200 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | |||||
chr11:65974371
|
C | CAAA | 17 | a0001c0002t0003g0244a0001c0005t0001g0158a0001c0006t0001g0142others(14): Show | 21 | HG00423.hp1 HG01069.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1573-2006_1573-200 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | |||||
chr11:65974371
|
CA | C | 8 | a0001c0002t0002g0035a0001c0002t0002g0231a0001c0004t0002g0018others(5): Show | 10 | HG02055.hp2 HG02155.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-2004delA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | |||||
chr11:65974371
|
CAA | C | 21 | a0001c0004t0002g0004a0001c0004t0002g0019a0001c0004t0002g0020others(18): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573-2005_1573-200 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | |||||
chr11:65974392
|
C | A | 117 | a0001c0002t0001g0036a0001c0005t0001g0007a0001c0005t0001g0012others(114): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1573-2003C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974392 | ||||||
chr11:65974395
|
T | C | 1 | a0001c0003t0003g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1573-2000T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974395 | ||||||
chr11:65974402
|
C | A | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1573-1993C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974402 | ||||||
chr11:65974462
|
C | T | 1 | a0001c0003t0002g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1573-1933C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974462 | ||||||
chr11:65974633
|
C | T | 1 | a0001c0002t0003g0229 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1573-1762C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974633 | ||||||
chr11:65974713
|
C | T | 2 | a0001c0002t0002g0181a0001c0003t0002g0067 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1573-1682C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974713 | ||||||
chr11:65974772
|
A | G | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1573-1623A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974772 | ||||||
chr11:65974812
|
A | G | 74 | a0001c0002t0002g0233a0001c0002t0003g0002a0001c0002t0003g0015others(71): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1573-1583A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974812 | ||||||
chr11:65974851
|
C | T | 1 | a0002c0001t0001g0121 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1573-1544C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974851 | ||||||
chr11:65974852
|
G | A | 4 | a0001c0005t0002g0042a0001c0005t0002g0260a0001c0005t0002g0261others(1): Show | 4 | HG01106.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573-1543G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974852 | ||||||
chr11:65974900
|
C | T | 1 | a0001c0003t0005g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1573-1495C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974900 | ||||||
chr11:65974901
|
G | C | 1 | a0001c0003t0004g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1573-1494G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974901 | ||||||
chr11:65974911
|
G | C | 3 | a0001c0002t0002g0222a0001c0002t0002g0227a0001c0002t0002g0257 | 3 | HG00642.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1573-1484G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974911 | ||||||
chr11:65974946
|
A | C | 3 | a0003c0008t0002g0050a0003c0008t0002g0051a0003c0008t0002g0052 | 3 | NA18950.hp2 NA18984.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1573-1449A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974946 | ||||||
chr11:65974955
|
C | G | 270 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(267): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1573-1440C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974955 | ||||||
chr11:65975061
|
GACAA | G | 1 | a0002c0001t0001g0011 | 3 | NA18961.hp2 NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1573-1320_1573-131 others(8): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975061 | |||||
chr11:65975065
|
A | G | 1 | a0001c0003t0010g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1573-1330A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975065 | ||||||
chr11:65975101
|
C | CT | 41 | a0001c0002t0002g0207a0001c0002t0002g0218a0001c0002t0002g0240others(38): Show | 59 | HG00673.hp1 HG01106.hp1 HG01433.hp2 others(56): Show |
intron_variant | MODIFIER | c.1573-1275dupT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975101 | |||||
chr11:65975101
|
C | CTT | 5 | a0001c0004t0002g0019a0001c0004t0002g0055a0001c0004t0002g0070others(2): Show | 6 | HG02074.hp2 HG02647.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1573-1276_1573-127 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975101 | |||||
chr11:65975367
|
T | C | 118 | a0001c0002t0001g0036a0001c0005t0001g0007a0001c0005t0001g0012others(115): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1573-1028T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975367 | ||||||
chr11:65975410
|
A | AT | 180 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(177): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1573-965dupT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975410 | |||||
chr11:65975410
|
A | ATT | 10 | a0001c0002t0002g0218a0001c0002t0002g0231a0001c0003t0002g0162others(7): Show | 10 | HG01109.hp1 HG03098.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-966_1573-965d others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975410 | |||||
chr11:65975430
|
T | C | 1 | a0003c0008t0002g0050 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1573-965T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975430 | ||||||
chr11:65975430
|
T | TC | 23 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(20): Show | 34 | HG00673.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1573-964dupC | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975430 | |||||
chr11:65975462
|
T | C | 113 | a0001c0002t0001g0036a0001c0002t0003g0236a0001c0005t0001g0007others(110): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1573-933T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975462 | ||||||
chr11:65975632
|
C | T | 5 | a0002c0001t0001g0011a0002c0001t0001g0118a0002c0001t0001g0130others(2): Show | 7 | HG00673.hp2 HG02027.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573-763C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975632 | ||||||
chr11:65975652
|
C | T | 1 | a0002c0001t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1573-743C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975652 | ||||||
chr11:65975809
|
T | C | 1 | a0001c0002t0003g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1573-586T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975809 | ||||||
chr11:65976039
|
G | A | 26 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(23): Show | 37 | HG00673.hp1 HG01891.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1573-356G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976039 | ||||||
chr11:65976040
|
G | A | 20 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(17): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573-355G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976040 | ||||||
chr11:65976049
|
G | A | 5 | a0001c0003t0002g0162a0001c0003t0002g0163a0001c0003t0002g0164others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1573-346G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976049 | ||||||
chr11:65976260
|
A | C | 1 | a0001c0003t0003g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1573-135A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976260 | ||||||
chr11:65976278
|
C | A | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1573-117C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976278 | ||||||
chr11:65976280
|
T | G | 1 | a0002c0001t0001g0088 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1573-115T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976280 | ||||||
chr11:65976308
|
C | T | 2 | a0001c0003t0004g0013a0001c0003t0004g0168 | 4 | HG01243.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573-87C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976308 | ||||||
chr11:65976633
|
G | C | 1 | a0001c0002t0002g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1747-23G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 13/19 | chr11 | 65976633 | ||||||
chr11:65976776
|
G | A | 46 | a0001c0002t0002g0008a0001c0002t0002g0010a0001c0002t0002g0031others(43): Show | 56 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1857+10G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976776 | ||||||
chr11:65976780
|
C | T | 1 | a0002c0001t0001g0128 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1857+14C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976780 | ||||||
chr11:65976794
|
C | T | 41 | a0002c0001t0001g0003a0002c0001t0001g0011a0002c0001t0001g0028others(38): Show | 55 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1857+28C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976794 | ||||||
chr11:65976804
|
T | C | 197 | a0001c0002t0001g0036a0001c0002t0002g0233a0001c0002t0003g0002others(194): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1857+38T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976804 | ||||||
chr11:65976832
|
C | T | 20 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(17): Show | 31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1857+66C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976832 | ||||||
chr11:65976950
|
C | T | 119 | a0001c0002t0001g0036a0001c0005t0001g0007a0001c0005t0001g0012others(116): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1858-64C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976950 | ||||||
chr11:65977126
|
C | T | 47 | a0001c0002t0002g0233a0001c0002t0003g0002a0001c0002t0003g0015others(44): Show | 67 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1945+25C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977126 | ||||||
chr11:65977165
|
C | T | 1 | a0001c0002t0003g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1945+64C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977165 | ||||||
chr11:65977266
|
G | A | 1 | a0001c0002t0003g0252 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1945+165G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977266 | ||||||
chr11:65977414
|
C | T | 1 | a0002c0001t0001g0119 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1946-149C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977414 | ||||||
chr11:65977550
|
C | T | 1 | a0001c0003t0003g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1946-13C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977550 | ||||||
chr11:65977760
|
C | T | 17 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(14): Show | 27 | HG00673.hp1 HG02074.hp2 HG02080.hp1 others(24): Show |
splice_region_variant&intron_variant | LOW | c.2037-4C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 16/19 | chr11 | 65977760 | ||||||
chr11:65977922
|
G | A | 9 | a0001c0005t0001g0007a0001c0005t0001g0012a0001c0005t0001g0022others(6): Show | 17 | HG01934.hp1 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2172+23G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65977922 | ||||||
chr11:65977932
|
C | G | 7 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(4): Show | 8 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2172+33C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65977932 | ||||||
chr11:65977955
|
AGGGCCAT others(10): Show |
A | 1 | a0002c0001t0001g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2172+74_2172+90del others(17): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr11 | 65977955 | |||||
chr11:65978017
|
T | C | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2172+118T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978017 | ||||||
chr11:65978145
|
G | A | 1 | a0008c0013t0001g0089 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2172+246G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978145 | ||||||
chr11:65978255
|
G | C | 273 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(270): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.2173-345G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978255 | ||||||
chr11:65978283
|
T | A | 6 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173-317T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978283 | ||||||
chr11:65978305
|
T | TCCAGCC | 16 | a0001c0004t0002g0004a0001c0004t0002g0018a0001c0004t0002g0019others(13): Show | 26 | HG00673.hp1 HG02074.hp2 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.2173-295_2173-294i others(8): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978305 | ||||||
chr11:65978306
|
G | C | 273 | a0001c0002t0001g0036a0001c0002t0002g0008a0001c0002t0002g0010others(270): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.2173-294G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978306 | ||||||
chr11:65978390
|
C | T | 1 | a0001c0005t0002g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2173-210C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978390 | ||||||
chr11:65978415
|
C | T | 1 | a0001c0002t0003g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2173-185C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978415 | ||||||
chr11:65978417
|
G | A | 4 | a0001c0003t0003g0059a0001c0003t0003g0061a0001c0003t0003g0062others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2173-183G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978417 | ||||||
chr11:65978418
|
G | A | 1 | a0001c0002t0003g0040 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2173-182G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978418 | ||||||
chr11:65978460
|
T | C | 5 | a0002c0001t0001g0009a0002c0001t0001g0081a0002c0001t0001g0094others(2): Show | 8 | HG00423.hp2 HG02523.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.2173-140T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978460 | ||||||
chr11:65978467
|
C | G | 1 | a0001c0003t0004g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2173-133C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978467 | ||||||
chr11:65978514
|
C | T | 18 | a0001c0003t0002g0014a0001c0003t0002g0176a0001c0003t0002g0178others(15): Show | 19 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2173-86C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978514 | ||||||
chr11:65978552
|
C | T | 5 | a0001c0005t0002g0041a0001c0005t0002g0042a0001c0005t0002g0260others(2): Show | 6 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2173-48C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978552 | ||||||
chr11:65978713
|
G | T | 1 | a0001c0005t0002g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2262+24G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/19 | chr11 | 65978713 | ||||||
chr11:65978742
|
C | T | 2 | a0001c0004t0007g0068a0001c0004t0007g0069 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2263-51C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/19 | chr11 | 65978742 | ||||||
chr11:65978782
|
C | T | 1 | a0002c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2263-11C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/19 | chr11 | 65978782 | ||||||
chr11:65978937
|
G | C | 2 | a0001c0002t0002g0181a0001c0003t0002g0067 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2384+23G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978937 | ||||||
chr11:65978985
|
G | A | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2385-27G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978985 | ||||||
chr11:65978987
|
C | G | 3 | a0001c0004t0006g0045a0001c0004t0006g0046a0001c0004t0006g0047 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2385-25C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978987 | ||||||
chr11:65978992
|
G | T | 2 | a0001c0005t0002g0041a0001c0005t0002g0262 | 3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2385-20G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978992 |