geneid | 51768 |
---|---|
ensemblid | ENSG00000064115.11 |
hgncid | 23049 |
symbol | TM7SF3 |
name | transmembrane 7 superfamily member 3 |
refseq_nuc | NM_016551.3 |
refseq_prot | NP_057635.1 |
ensembl_nuc | ENST00000343028.9 |
ensembl_prot | ENSP00000342322.4 |
mane_status | MANE Select |
chr | chr12 |
start | 26971579 |
end | 27014384 |
strand | - |
ver | v1.2 |
region | chr12:26971579-27014384 |
region5000 | chr12:26966579-27019384 |
regionname0 | TM7SF3_chr12_26971579_27014384 |
regionname5000 | TM7SF3_chr12_26966579_27019384 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 570 | 381 | 73 | 64 | 181 | 16 | 45 | 142 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002 | 0/0 | 570 | 31 | 2 | 7 | 22 | 0 | 0 | 19 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0003 | 0/0 | 570 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0004 | 0/0 | 570 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0005 | 0/0 | 570 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0006 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0007 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0008 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0009 | 0/0 | 570 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1713 | 379 | 73 | 64 | 179 | 16 | 45 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0002 | 0/0 | 1713 | 31 | 2 | 7 | 22 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0003 | 0/0 | 1713 | 9 | 9 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0004 | 0/0 | 1713 | 3 | 0 | 1 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0005 | 0/0 | 1713 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0006 | 0/0 | 1713 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0007 | 0/0 | 1713 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0008 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0009 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
c0010 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2603 | 117 | 24 | 10 | 65 | 3 | 15 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0002 | 0/0 | 2604 | 57 | 4 | 20 | 23 | 2 | 8 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0003 | 0/0 | 2604 | 51 | 6 | 2 | 37 | 1 | 5 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0004 | 0/0 | 2600 | 50 | 6 | 7 | 31 | 3 | 3 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0005 | 0/0 | 2604 | 32 | 0 | 8 | 24 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0006 | 0/0 | 2604 | 31 | 6 | 12 | 2 | 3 | 8 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0007 | 0/1 | 2604 | 14 | 5 | 4 | 0 | 2 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0008 | 1/0 | 2603 | 11 | 3 | 5 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0009 | 0/0 | 2604 | 9 | 9 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0010 | 0/0 | 2603 | 6 | 1 | 2 | 0 | 1 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0011 | 0/0 | 2602 | 5 | 0 | 0 | 5 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0012 | 0/0 | 2605 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0013 | 0/0 | 2603 | 4 | 4 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0014 | 0/0 | 2604 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0015 | 0/0 | 2603 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0016 | 0/0 | 2603 | 3 | 1 | 1 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0017 | 0/0 | 2602 | 3 | 1 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0018 | 0/0 | 2604 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0019 | 0/0 | 2603 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0020 | 0/0 | 2603 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0021 | 0/0 | 2604 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0022 | 0/0 | 2603 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0023 | 0/0 | 2604 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0024 | 0/0 | 2604 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0025 | 0/0 | 2605 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0026 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0027 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0028 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0029 | 0/0 | 2603 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0030 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0031 | 0/0 | 2605 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0032 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0033 | 0/0 | 2605 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0034 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0035 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0036 | 0/0 | 2603 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0037 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0038 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0039 | 0/0 | 2604 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
t0040 | 0/0 | 2603 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0002 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0356 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1713 | 379 | 73 | 64 | 179 | 16 | 45 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0005 | 0/0 | 1713 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002 | 0/0 | 1713 | 31 | 2 | 7 | 22 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0003c0003 | 0/0 | 1713 | 9 | 9 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0004c0004 | 0/0 | 1713 | 3 | 0 | 1 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0005c0006 | 0/0 | 1713 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0006c0010 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0007c0008 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0008c0009 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0009c0007 | 0/0 | 1713 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4315 | 113 | 24 | 10 | 61 | 3 | 15 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0002 | 0/0 | 4316 | 57 | 4 | 20 | 23 | 2 | 8 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0003 | 0/0 | 4316 | 50 | 6 | 2 | 36 | 1 | 5 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0004 | 0/0 | 4312 | 46 | 4 | 7 | 30 | 3 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0005 | 0/0 | 4316 | 12 | 0 | 1 | 11 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0006 | 0/0 | 4316 | 31 | 6 | 12 | 2 | 3 | 8 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0007 | 0/1 | 4316 | 14 | 5 | 4 | 0 | 2 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0008 | 1/0 | 4315 | 11 | 3 | 5 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0010 | 0/0 | 4315 | 4 | 1 | 2 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0011 | 0/0 | 4314 | 5 | 0 | 0 | 5 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0013 | 0/0 | 4315 | 4 | 4 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0014 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0015 | 0/0 | 4315 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0016 | 0/0 | 4315 | 2 | 1 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0017 | 0/0 | 4314 | 3 | 1 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0018 | 0/0 | 4316 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0019 | 0/0 | 4315 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0020 | 0/0 | 4315 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0024 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0025 | 0/0 | 4317 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0026 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0027 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0028 | 0/0 | 4315 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0029 | 0/0 | 4315 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0030 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0031 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0032 | 0/0 | 4313 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0033 | 0/0 | 4317 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0034 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0035 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0037 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0038 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0039 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0001t0040 | 0/0 | 4315 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0001c0005t0005 | 0/0 | 4316 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0001 | 0/0 | 4315 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0004 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0005 | 0/0 | 4316 | 18 | 0 | 7 | 11 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0012 | 0/0 | 4317 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0014 | 0/0 | 4316 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0021 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0022 | 0/0 | 4315 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0002c0002t0023 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0003c0003t0009 | 0/0 | 4316 | 9 | 9 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0004c0004t0010 | 0/0 | 4315 | 2 | 0 | 0 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0004c0004t0016 | 0/0 | 4315 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0005c0006t0004 | 0/0 | 4312 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0006c0010t0003 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0007c0008t0036 | 0/0 | 4315 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0008c0009t0001 | 0/0 | 4315 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
a0009c0007t0004 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | copy fasta | chr12 | 26966579 | 27019384 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0002 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0005g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0006g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0356 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0008g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0010g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0010g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0011g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0011g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0011g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0013g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0017g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0017g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0017g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0018g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0019g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0019g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0020g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0020g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0024g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0025g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0026g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0027g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0028g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0029g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0030g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0031g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0032g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0033g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0034g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0035g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0037g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0038g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0039g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0001t0040g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0005t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0001c0005t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0004g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0005g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0012g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0012g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0012g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0014g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0014g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0021g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0022g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0002c0002t0023g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0003c0003t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0004c0004t0010g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0004c0004t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0004c0004t0016g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0005c0006t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0005c0006t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0006c0010t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0007c0008t0036g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0008c0009t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
a0009c0007t0004g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0050 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0063 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00280 | hp2 | a0001 | c0001 | t0010 | g0255 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00323 | hp2 | a0001 | c0001 | t0006 | g0061 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00558 | hp2 | a0001 | c0001 | t0019 | g0275 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0152 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0064 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00738 | hp1 | a0004 | c0004 | t0016 | g0224 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0230 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01069 | hp1 | a0002 | c0002 | t0005 | g0374 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0161 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0065 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01071 | hp1 | a0002 | c0002 | t0005 | g0026 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0309 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0028 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0051 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0200 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01109 | hp1 | a0002 | c0002 | t0005 | g0337 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01109 | hp2 | a0001 | c0001 | t0025 | g0052 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0158 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0213 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01175 | hp2 | a0001 | c0001 | t0008 | g0082 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0362 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0048 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01261 | hp2 | a0001 | c0001 | t0010 | g0256 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0049 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01358 | hp2 | a0001 | c0001 | t0008 | g0353 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0033 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0058 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0013 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0062 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0013 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01928 | hp1 | a0002 | c0002 | t0005 | g0338 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0351 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0360 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01993 | hp1 | a0002 | c0002 | t0005 | g0373 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02004 | hp2 | a0002 | c0002 | t0005 | g0022 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02015 | hp2 | a0001 | c0001 | t0039 | g0047 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02027 | hp2 | a0002 | c0002 | t0005 | g0254 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02055 | hp1 | a0001 | c0001 | t0026 | g0150 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0333 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0364 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0070 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0287 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02135 | hp2 | a0002 | c0002 | t0005 | g0379 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02145 | hp2 | a0001 | c0001 | t0028 | g0151 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0346 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0335 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0078 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02300 | hp2 | a0002 | c0002 | t0005 | g0026 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02451 | hp1 | a0003 | c0003 | t0009 | g0006 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02523 | hp1 | a0001 | c0001 | t0016 | g0092 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02523 | hp2 | a0001 | c0001 | t0038 | g0308 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0239 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02572 | hp2 | a0001 | c0001 | t0013 | g0262 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0017 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0376 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0162 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0128 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0261 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02723 | hp2 | a0002 | c0002 | t0014 | g0372 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02809 | hp2 | a0001 | c0001 | t0020 | g0375 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02886 | hp1 | a0003 | c0003 | t0009 | g0233 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02897 | hp2 | a0001 | c0001 | t0037 | g0130 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02922 | hp2 | a0001 | c0001 | t0027 | g0231 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02965 | hp1 | a0003 | c0003 | t0009 | g0234 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02976 | hp2 | a0003 | c0003 | t0009 | g0237 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03017 | hp2 | a0001 | c0001 | t0035 | g0032 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03041 | hp2 | a0002 | c0002 | t0014 | g0363 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0355 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0079 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03209 | hp1 | a0003 | c0003 | t0009 | g0232 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0148 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0226 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0246 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03453 | hp1 | a0001 | c0001 | t0018 | g0127 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03453 | hp2 | a0001 | c0001 | t0014 | g0081 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0329 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0017 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03491 | hp1 | a0004 | c0004 | t0010 | g0253 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03492 | hp2 | a0004 | c0004 | t0010 | g0252 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0080 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03516 | hp2 | a0003 | c0003 | t0009 | g0006 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0164 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0225 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03669 | hp1 | a0001 | c0001 | t0040 | g0390 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0067 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0350 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0075 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0332 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0074 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03831 | hp2 | a0009 | c0007 | t0004 | g0365 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0244 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0193 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0366 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0109 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0357 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0066 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG04228 | hp2 | a0001 | c0001 | t0033 | g0059 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18906 | hp1 | a0003 | c0003 | t0009 | g0236 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18906 | hp2 | a0005 | c0006 | t0004 | g0186 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18946 | hp1 | a0001 | c0001 | t0024 | g0195 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18949 | hp1 | a0002 | c0002 | t0005 | g0371 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18952 | hp2 | a0001 | c0005 | t0005 | g0167 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18956 | hp2 | a0002 | c0002 | t0005 | g0383 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18966 | hp2 | a0002 | c0002 | t0005 | g0380 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18968 | hp1 | a0002 | c0002 | t0005 | g0385 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18973 | hp1 | a0006 | c0010 | t0003 | g0110 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18975 | hp1 | a0001 | c0001 | t0019 | g0276 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18977 | hp2 | a0002 | c0002 | t0005 | g0197 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18981 | hp1 | a0001 | c0001 | t0032 | g0311 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18984 | hp1 | a0001 | c0001 | t0017 | g0265 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18989 | hp1 | a0002 | c0002 | t0012 | g0388 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18991 | hp2 | a0001 | c0001 | t0011 | g0286 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18992 | hp1 | a0002 | c0002 | t0022 | g0384 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18999 | hp1 | a0002 | c0002 | t0023 | g0381 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19000 | hp1 | a0001 | c0001 | t0031 | g0191 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19002 | hp2 | a0001 | c0001 | t0017 | g0331 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19003 | hp2 | a0007 | c0008 | t0036 | g0133 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19006 | hp2 | a0001 | c0001 | t0011 | g0300 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19010 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19012 | hp1 | a0001 | c0001 | t0011 | g0348 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0377 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19055 | hp1 | a0008 | c0009 | t0001 | g0263 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19057 | hp2 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19060 | hp2 | a0002 | c0002 | t0005 | g0378 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19062 | hp2 | a0002 | c0002 | t0005 | g0022 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19064 | hp1 | a0001 | c0005 | t0005 | g0165 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19067 | hp2 | a0002 | c0002 | t0005 | g0382 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19068 | hp2 | a0002 | c0002 | t0012 | g0016 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19076 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19077 | hp1 | a0001 | c0001 | t0011 | g0349 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19078 | hp1 | a0002 | c0002 | t0005 | g0389 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19080 | hp1 | a0001 | c0001 | t0034 | g0285 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19081 | hp1 | a0001 | c0001 | t0011 | g0289 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19082 | hp2 | a0002 | c0002 | t0012 | g0387 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19084 | hp2 | a0002 | c0002 | t0012 | g0016 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19089 | hp2 | a0002 | c0002 | t0021 | g0339 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19091 | hp1 | a0002 | c0002 | t0004 | g0386 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19240 | hp1 | a0003 | c0003 | t0009 | g0006 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20752 | hp2 | a0001 | c0001 | t0029 | g0326 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0160 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0053 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0068 | SAS | GIH | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | GIH | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG01123 | hp2 | a0001 | c0001 | t0008 | g0352 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02109 | hp1 | a0001 | c0001 | t0020 | g0361 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0354 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0251 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0126 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG06807 | hp1 | a0005 | c0006 | t0004 | g0187 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20300 | hp1 | a0003 | c0003 | t0009 | g0235 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0245 | REF | REF | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0356 | REF | REF | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:26990518
|
G | A | 1 | a0004 | 3 | HG00738.hp1 HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.800C>T | p.Ala267Val | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 1016/4315 | 800/1713 | 267/570 | chr12 | 26990518 | ||
chr12:26990539
|
T | G | 1 | a0007 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.779A>C | p.Asp260Ala | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 995/4315 | 779/1713 | 260/570 | chr12 | 26990539 | ||
chr12:26990540
|
C | T | 1 | a0007 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.778G>A | p.Asp260Asn | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 994/4315 | 778/1713 | 260/570 | chr12 | 26990540 | ||
chr12:26990543
|
A | C | 1 | a0007 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.775T>G | p.Trp259Gly | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 991/4315 | 775/1713 | 259/570 | chr12 | 26990543 | ||
chr12:26990575
|
G | A | 1 | a0002 | 31 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
missense_variant | MODERATE | c.743C>T | p.Pro248Leu | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 959/4315 | 743/1713 | 248/570 | chr12 | 26990575 | ||
chr12:26995244
|
G | A | 1 | a0005 | 2 | HG06807.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.683C>T | p.Ala228Val | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/12 | 899/4315 | 683/1713 | 228/570 | chr12 | 26995244 | ||
chr12:26995391
|
G | C | 1 | a0003 | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
missense_variant | MODERATE | c.536C>G | p.Pro179Arg | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/12 | 752/4315 | 536/1713 | 179/570 | chr12 | 26995391 | ||
chr12:26996745
|
G | A | 1 | a0008 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.515C>T | p.Ala172Val | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/12 | 731/4315 | 515/1713 | 172/570 | chr12 | 26996745 | ||
chr12:26996781
|
G | A | 1 | a0006 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.479C>T | p.Thr160Met | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/12 | 695/4315 | 479/1713 | 160/570 | chr12 | 26996781 | ||
chr12:27003328
|
C | G | 1 | a0009 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.154G>C | p.Glu52Gln | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/12 | 370/4315 | 154/1713 | 52/570 | chr12 | 27003328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:26990466
|
A | T | 1 | a0001c0005 | 2 | NA18952.hp2 NA19064.hp1 |
synonymous_variant | LOW | c.852T>A | p.Gly284Gly | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 1068/4315 | 852/1713 | 284/570 | chr12 | 26990466 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:26971595
|
GATTT | G | 9 | a0001c0001t0004a0001c0001t0032a0001c0001t0034others(6): Show | 55 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2369delAAAT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2366 | chr12 | 26971595 | |||||
chr12:26971660
|
G | A | 1 | a0001c0001t0027 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2305 | chr12 | 26971660 | |||||
chr12:26971721
|
T | C | 4 | a0001c0001t0014a0001c0001t0026a0001c0001t0028others(1): Show | 5 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2244A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2244 | chr12 | 26971721 | |||||
chr12:26971722
|
A | G | 5 | a0001c0001t0006a0001c0001t0015a0001c0001t0018others(2): Show | 39 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2243T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2243 | chr12 | 26971722 | |||||
chr12:26971806
|
C | A | 1 | a0001c0001t0007 | 14 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2159G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2159 | chr12 | 26971806 | |||||
chr12:26971851
|
T | C | 4 | a0001c0001t0006a0001c0001t0018a0001c0001t0033others(1): Show | 36 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2114A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2114 | chr12 | 26971851 | |||||
chr12:26971943
|
T | G | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
3_prime_UTR_variant | MODIFIER | c.*2022A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2022 | chr12 | 26971943 | |||||
chr12:26972058
|
A | G | 1 | a0001c0001t0035 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1907 | chr12 | 26972058 | |||||
chr12:26972420
|
CT | C | 16 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(13): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1544delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1544 | chr12 | 26972420 | |||||
chr12:26972438
|
C | T | 2 | a0001c0001t0010a0004c0004t0010 | 6 | HG00280.hp2 HG01175.hp1 HG01261.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1527G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1527 | chr12 | 26972438 | |||||
chr12:26972452
|
G | A | 1 | a0001c0001t0019 | 2 | HG00558.hp2 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1513 | chr12 | 26972452 | |||||
chr12:26972477
|
G | A | 1 | a0003c0003t0009 | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1488 | chr12 | 26972477 | |||||
chr12:26972527
|
T | C | 1 | a0001c0001t0029 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1438A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1438 | chr12 | 26972527 | |||||
chr12:26972800
|
T | C | 1 | a0001c0001t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1165 | chr12 | 26972800 | |||||
chr12:26972870
|
G | A | 1 | a0001c0001t0038 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1095 | chr12 | 26972870 | |||||
chr12:26972959
|
CA | C | 1 | a0001c0001t0011 | 5 | NA18991.hp2 NA19006.hp2 NA19012.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1005delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1005 | chr12 | 26972959 | |||||
chr12:26973006
|
G | A | 1 | a0001c0001t0020 | 2 | HG02109.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 959 | chr12 | 26973006 | |||||
chr12:26973023
|
A | G | 1 | a0001c0001t0034 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*942T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 942 | chr12 | 26973023 | |||||
chr12:26973109
|
G | A | 1 | a0001c0001t0039 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 856 | chr12 | 26973109 | |||||
chr12:26973169
|
A | C | 2 | a0001c0001t0014a0002c0002t0014 | 3 | HG02723.hp2 HG03041.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*796T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 796 | chr12 | 26973169 | |||||
chr12:26973175
|
G | GT | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*789dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 789 | chr12 | 26973175 | |||||
chr12:26973175
|
G | GTT | 6 | a0001c0001t0025a0001c0001t0026a0001c0001t0031others(3): Show | 9 | HG01109.hp2 HG02055.hp1 HG04228.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*789dupAA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 789 | chr12 | 26973175 | |||||
chr12:26973179
|
T | G | 1 | a0001c0001t0020 | 2 | HG02109.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*786A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 786 | chr12 | 26973179 | |||||
chr12:26973179
|
T | TG | 2 | a0001c0001t0018a0002c0002t0023 | 4 | HG02717.hp1 HG03453.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786insC | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 785 | chr12 | 26973179 | |||||
chr12:26973237
|
A | G | 1 | a0002c0002t0021 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 728 | chr12 | 26973237 | |||||
chr12:26973263
|
T | G | 18 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(15): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*702A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 702 | chr12 | 26973263 | |||||
chr12:26973335
|
G | A | 1 | a0001c0001t0013 | 4 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*630C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 630 | chr12 | 26973335 | |||||
chr12:26973367
|
G | T | 1 | a0001c0001t0024 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*598C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 598 | chr12 | 26973367 | |||||
chr12:26973743
|
A | G | 7 | a0001c0001t0005a0001c0005t0005a0002c0002t0005others(4): Show | 39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*222T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 222 | chr12 | 26973743 | |||||
chr12:27014233
|
C | A | 1 | a0001c0001t0040 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-65G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/12 | 65 | chr12 | 27014233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:26974392
|
T | C | 1 | a0001c0001t0016g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1451-165A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26974392 | ||||||
chr12:26974704
|
C | T | 46 | a0001c0001t0002g0090a0001c0001t0002g0107a0001c0001t0003g0004others(43): Show | 51 | HG00099.hp2 HG00642.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1451-477G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26974704 | ||||||
chr12:26974711
|
A | G | 1 | a0001c0001t0003g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1451-484T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26974711 | ||||||
chr12:26975078
|
ACT | A | 36 | a0001c0001t0005g0098a0001c0001t0005g0100a0001c0001t0005g0104others(33): Show | 39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1450+416_1450+417d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26975078 | ||||||
chr12:26975341
|
C | T | 1 | a0001c0001t0004g0160 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1450+155G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26975341 | ||||||
chr12:26975395
|
T | C | 1 | a0001c0001t0004g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1450+101A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26975395 | ||||||
chr12:26975661
|
G | GT | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
splice_region_variant&intron_variant | LOW | c.1288-4dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26975661 | ||||||
chr12:26975791
|
C | A | 1 | a0001c0001t0004g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1288-133G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26975791 | ||||||
chr12:26975814
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1288-156T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26975814 | ||||||
chr12:26976018
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1287+242A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26976018 | ||||||
chr12:26976105
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(1): Show | 4 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+155C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26976105 | ||||||
chr12:26976204
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1287+56T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26976204 | ||||||
chr12:26976440
|
T | C | 1 | a0002c0002t0005g0338 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1190-83A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26976440 | ||||||
chr12:26976453
|
T | C | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1190-96A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26976453 | ||||||
chr12:26976582
|
C | G | 1 | a0001c0001t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1190-225G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26976582 | ||||||
chr12:26977016
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1190-659T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977016 | ||||||
chr12:26977153
|
T | C | 2 | a0001c0001t0004g0131a0001c0001t0037g0130 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1190-796A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977153 | ||||||
chr12:26977232
|
C | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1190-875G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977232 | ||||||
chr12:26977293
|
G | C | 1 | a0001c0001t0006g0048 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1190-936C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977293 | ||||||
chr12:26977396
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1190-1039T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977396 | ||||||
chr12:26977408
|
A | G | 1 | a0002c0002t0023g0381 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1190-1051T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977408 | ||||||
chr12:26977520
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1190-1163C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977520 | ||||||
chr12:26977702
|
T | C | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.1190-1345A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977702 | ||||||
chr12:26977766
|
ATG | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1190-1411_1190-141 others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977766 | ||||||
chr12:26977766
|
ATGTG | A | 114 | a0001c0001t0002g0014a0001c0001t0002g0023a0001c0001t0002g0024others(111): Show | 123 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1190-1413_1190-141 others(8): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977766 | ||||||
chr12:26977946
|
G | A | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.1190-1589C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977946 | ||||||
chr12:26978506
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02155.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1189+1278G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978506 | ||||||
chr12:26978627
|
A | G | 37 | a0001c0001t0006g0028a0001c0001t0006g0042a0001c0001t0006g0043others(34): Show | 37 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1189+1157T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978627 | ||||||
chr12:26978634
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0279a0001c0001t0001g0280others(7): Show | 11 | HG00597.hp2 HG01257.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189+1150A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978634 | ||||||
chr12:26978744
|
AT | A | 94 | a0001c0001t0001g0259a0001c0001t0002g0014a0001c0001t0002g0023others(91): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1189+1039delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978744 | ||||||
chr12:26978744
|
ATT | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1189+1038_1189+103 others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978744 | ||||||
chr12:26978976
|
A | C | 3 | a0001c0001t0014g0081a0002c0002t0014g0363a0002c0002t0014g0372 | 3 | HG02723.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1189+808T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978976 | ||||||
chr12:26979013
|
G | GA | 12 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0096others(9): Show | 14 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1189+770dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979013 | ||||||
chr12:26979021
|
A | C | 3 | a0001c0001t0002g0035a0001c0001t0002g0054a0001c0001t0002g0202 | 3 | HG00280.hp1 HG00738.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1189+763T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979021 | ||||||
chr12:26979025
|
C | T | 1 | a0001c0001t0004g0364 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1189+759G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979025 | ||||||
chr12:26979096
|
A | G | 36 | a0001c0001t0005g0098a0001c0001t0005g0100a0001c0001t0005g0104others(33): Show | 39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1189+688T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979096 | ||||||
chr12:26979174
|
C | T | 1 | a0001c0001t0014g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1189+610G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979174 | ||||||
chr12:26979281
|
T | C | 1 | a0001c0001t0016g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1189+503A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979281 | ||||||
chr12:26979309
|
T | A | 2 | a0001c0001t0002g0173a0001c0001t0002g0204 | 2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1189+475A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979309 | ||||||
chr12:26979510
|
C | T | 1 | a0004c0004t0016g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1189+274G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979510 | ||||||
chr12:26979758
|
C | CA | 96 | a0001c0001t0002g0090a0001c0001t0002g0107a0001c0001t0002g0132others(93): Show | 104 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.1189+25dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979758 | ||||||
chr12:26979989
|
C | T | 1 | a0001c0001t0030g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1037-53G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26979989 | ||||||
chr12:26980018
|
G | C | 1 | a0001c0001t0017g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1037-82C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980018 | ||||||
chr12:26980060
|
T | C | 36 | a0001c0001t0005g0098a0001c0001t0005g0100a0001c0001t0005g0104others(33): Show | 39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1037-124A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980060 | ||||||
chr12:26980134
|
A | G | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1037-198T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980134 | ||||||
chr12:26980150
|
C | T | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1037-214G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980150 | ||||||
chr12:26980292
|
A | G | 1 | a0002c0002t0023g0381 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1036+274T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980292 | ||||||
chr12:26980516
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1036+50G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980516 | ||||||
chr12:26980835
|
A | G | 1 | a0001c0001t0006g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.956-189T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26980835 | ||||||
chr12:26980894
|
A | G | 1 | a0001c0001t0002g0344 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.956-248T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26980894 | ||||||
chr12:26981142
|
A | G | 2 | a0001c0001t0018g0126a0001c0001t0018g0128 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.956-496T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981142 | ||||||
chr12:26981548
|
C | T | 1 | a0002c0002t0005g0389 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.956-902G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981548 | ||||||
chr12:26981856
|
A | G | 152 | a0001c0001t0002g0014a0001c0001t0002g0023a0001c0001t0002g0024others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.955+917T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981856 | ||||||
chr12:26981868
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.955+905A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981868 | ||||||
chr12:26981931
|
A | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.955+842T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981931 | ||||||
chr12:26981981
|
C | T | 2 | a0001c0001t0007g0008a0001c0001t0007g0051 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.955+792G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981981 | ||||||
chr12:26982426
|
C | T | 1 | a0004c0004t0016g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.955+347G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982426 | ||||||
chr12:26982472
|
C | T | 1 | a0001c0001t0003g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.955+301G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982472 | ||||||
chr12:26982498
|
C | T | 2 | a0001c0001t0003g0106a0001c0001t0003g0211 | 2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.955+275G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982498 | ||||||
chr12:26982587
|
C | T | 15 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0135others(12): Show | 15 | NA18943.hp2 NA18946.hp1 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.955+186G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982587 | ||||||
chr12:26982736
|
T | G | 58 | a0001c0001t0001g0096a0001c0001t0002g0090a0001c0001t0002g0107others(55): Show | 63 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.955+37A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982736 | ||||||
chr12:26982861
|
T | TA | 12 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0178others(9): Show | 13 | HG00642.hp1 HG02109.hp1 HG02809.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.869-3dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982861 | ||||||
chr12:26982969
|
C | T | 9 | a0001c0001t0003g0119a0001c0001t0004g0083a0001c0001t0004g0085others(6): Show | 9 | HG00558.hp1 HG00673.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.869-110G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982969 | ||||||
chr12:26982979
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.869-120A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982979 | ||||||
chr12:26982985
|
A | G | 58 | a0001c0001t0001g0096a0001c0001t0002g0090a0001c0001t0002g0107others(55): Show | 63 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.869-126T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982985 | ||||||
chr12:26983247
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.869-388C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983247 | ||||||
chr12:26983320
|
A | T | 1 | a0001c0001t0017g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.869-461T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983320 | ||||||
chr12:26983332
|
ATTCAAAC others(6): Show |
A | 1 | a0001c0001t0003g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.869-486_869-474del others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983332 | ||||||
chr12:26983339
|
C | T | 1 | a0001c0001t0017g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.869-480G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983339 | ||||||
chr12:26983492
|
C | G | 1 | a0001c0001t0002g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.869-633G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983492 | ||||||
chr12:26983635
|
G | T | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.869-776C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983635 | ||||||
chr12:26983693
|
G | T | 30 | a0001c0001t0006g0042a0001c0001t0006g0043a0001c0001t0006g0056others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-834C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983693 | ||||||
chr12:26983721
|
C | T | 3 | a0001c0001t0002g0137a0001c0001t0002g0138a0007c0008t0036g0133 | 3 | NA18979.hp2 NA19000.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.869-862G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983721 | ||||||
chr12:26983726
|
A | G | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.869-867T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983726 | ||||||
chr12:26984060
|
C | T | 8 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0007g0008others(5): Show | 9 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.869-1201G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984060 | ||||||
chr12:26984151
|
C | T | 26 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.869-1292G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984151 | ||||||
chr12:26984168
|
G | A | 1 | a0001c0001t0030g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869-1309C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984168 | ||||||
chr12:26984205
|
G | A | 1 | a0001c0001t0025g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.869-1346C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984205 | ||||||
chr12:26984255
|
A | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 171 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.869-1396T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984255 | ||||||
chr12:26984257
|
C | T | 1 | a0004c0004t0016g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.869-1398G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984257 | ||||||
chr12:26984300
|
A | G | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.869-1441T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984300 | ||||||
chr12:26984355
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.869-1496C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984355 | ||||||
chr12:26984406
|
G | C | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.869-1547C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984406 | ||||||
chr12:26984442
|
C | T | 1 | a0002c0002t0023g0381 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.869-1583G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984442 | ||||||
chr12:26984449
|
C | CA | 30 | a0001c0001t0006g0074a0001c0001t0006g0162a0001c0001t0015g0080others(27): Show | 33 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.869-1591dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984449 | ||||||
chr12:26984449
|
C | CAA | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.869-1592_869-1591d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984449 | ||||||
chr12:26984477
|
C | T | 1 | a0001c0001t0004g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.869-1618G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984477 | ||||||
chr12:26984550
|
C | G | 1 | a0001c0001t0004g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.869-1691G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984550 | ||||||
chr12:26984639
|
C | T | 1 | a0001c0001t0006g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.869-1780G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984639 | ||||||
chr12:26984828
|
G | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00639.hp1 HG01243.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-1969C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984828 | ||||||
chr12:26984861
|
C | T | 4 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(1): Show | 4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2002G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984861 | ||||||
chr12:26985122
|
C | T | 57 | a0001c0001t0001g0101a0001c0001t0001g0112a0001c0001t0001g0243others(54): Show | 62 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.869-2263G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985122 | ||||||
chr12:26985129
|
A | G | 26 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.869-2270T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985129 | ||||||
chr12:26985201
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.869-2342C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985201 | ||||||
chr12:26985367
|
C | T | 4 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(1): Show | 4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2508G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985367 | ||||||
chr12:26985485
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.869-2626A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985485 | ||||||
chr12:26985621
|
CA | C | 22 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0002g0139others(19): Show | 24 | HG01433.hp1 HG01943.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.869-2763delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAA | C | 26 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(23): Show | 27 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.869-2764_869-2763d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0010g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.869-2773_869-2763d others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0003g0077a0001c0001t0005g0104a0001c0001t0006g0066others(2): Show | 5 | HG03471.hp2 HG04204.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-2774_869-2763d others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0108others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-2775_869-2763d others(15): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0003g0010a0001c0001t0003g0109a0001c0001t0003g0115others(4): Show | 8 | HG00099.hp2 HG01358.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.869-2776_869-2763d others(16): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0003g0216 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.869-2777_869-2763d others(17): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(9): Show |
C | 39 | a0001c0001t0001g0112a0001c0001t0002g0090a0001c0001t0002g0107others(36): Show | 41 | HG00597.hp1 HG00642.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.869-2778_869-2763d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0003g0099a0001c0001t0003g0102 | 2 | HG04204.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.869-2779_869-2763d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985621
|
CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0006g0075a0001c0001t0006g0333a0001c0001t0006g0351others(1): Show | 4 | HG01934.hp1 HG02015.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2780_869-2763d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | ||||||
chr12:26985635
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0016g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.869-2795_869-2777d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985635 | ||||||
chr12:26985636
|
AAAAAAAA others(11): Show |
A | 14 | a0001c0001t0006g0042a0001c0001t0006g0043a0001c0001t0006g0049others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.869-2795_869-2778d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985636 | ||||||
chr12:26985637
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.869-2795_869-2779d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985637 | ||||||
chr12:26985637
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0030g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869-2797_869-2779d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985637 | ||||||
chr12:26985638
|
AAAAAAAA others(9): Show |
A | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(5): Show | 10 | HG02074.hp1 HG02523.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-2795_869-2780d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985638 | ||||||
chr12:26985638
|
AAAAAAAA others(11): Show |
A | 6 | a0001c0001t0006g0048a0001c0001t0006g0058a0001c0001t0006g0069others(3): Show | 6 | HG00733.hp1 HG01256.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-2797_869-2780d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985638 | ||||||
chr12:26985638
|
AAAAAAAA others(21): Show |
A | 1 | a0004c0004t0016g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.869-2807_869-2780d others(30): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985638 | ||||||
chr12:26985639
|
AAAAAAAA others(10): Show |
A | 11 | a0001c0001t0001g0157a0001c0001t0001g0180a0001c0001t0001g0181others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.869-2797_869-2781d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985639 | ||||||
chr12:26985639
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0003g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.869-2799_869-2781d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985639 | ||||||
chr12:26985640
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0243a0001c0001t0004g0091 | 2 | HG00544.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.869-2797_869-2782d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985640 | ||||||
chr12:26985640
|
AAAAAAAA others(11): Show |
A | 6 | a0001c0001t0001g0073a0001c0001t0001g0182a0001c0001t0001g0248others(3): Show | 6 | HG02486.hp1 HG02922.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-2799_869-2782d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985640 | ||||||
chr12:26985641
|
AAAAAAAA others(8): Show |
A | 4 | a0001c0001t0001g0259a0001c0001t0001g0291a0001c0001t0001g0294others(1): Show | 4 | HG00438.hp2 NA18939.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2797_869-2783d others(17): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985641 | ||||||
chr12:26985641
|
AAAAAAAA others(10): Show |
A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 93 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.869-2799_869-2783d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985641 | ||||||
chr12:26985641
|
AAAAAAAA others(12): Show |
A | 3 | a0002c0002t0005g0380a0002c0002t0005g0382a0002c0002t0022g0384 | 3 | NA18966.hp2 NA18992.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.869-2801_869-2783d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985641 | ||||||
chr12:26985642
|
AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0001g0267a0001c0001t0001g0296a0001c0001t0001g0302 | 3 | HG00544.hp2 NA18943.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.869-2799_869-2784d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985642 | ||||||
chr12:26985642
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0323 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.869-2801_869-2784d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985642 | ||||||
chr12:26985642
|
AAAAAAAA others(13): Show |
A | 1 | a0002c0002t0004g0386 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.869-2803_869-2784d others(22): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985642 | ||||||
chr12:26985643
|
AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0019a0001c0001t0001g0192 | 3 | HG02602.hp1 NA18985.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.869-2799_869-2785d others(17): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985643 | ||||||
chr12:26985643
|
AAAAAAAA others(10): Show |
A | 10 | a0001c0001t0001g0146a0001c0001t0001g0279a0001c0001t0001g0280others(7): Show | 10 | HG00597.hp2 HG01257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-2801_869-2785d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985643 | ||||||
chr12:26985643
|
AAAAAAAA others(12): Show |
A | 19 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(16): Show | 22 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.869-2803_869-2785d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985643 | ||||||
chr12:26985644
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0027a0001c0001t0020g0361a0001c0001t0020g0375 | 3 | HG01496.hp2 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.869-2795_869-2786d others(12): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985644 | ||||||
chr12:26985644
|
AAAAAAAA others(9): Show |
A | 4 | a0001c0001t0001g0145a0001c0001t0001g0281a0001c0001t0001g0284others(1): Show | 4 | HG02145.hp1 HG04199.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2801_869-2786d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985644 | ||||||
chr12:26985644
|
AAAAAAAA others(11): Show |
A | 2 | a0002c0002t0005g0254a0002c0002t0005g0379 | 2 | HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.869-2803_869-2786d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985644 | ||||||
chr12:26985645
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0282 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.869-2803_869-2787d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985645 | ||||||
chr12:26985645
|
AAAAAAAA others(12): Show |
A | 1 | a0002c0002t0005g0337 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.869-2805_869-2787d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985645 | ||||||
chr12:26985646
|
A | T | 2 | a0001c0001t0002g0173a0001c0001t0027g0231 | 2 | HG02922.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.869-2787T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985646 | ||||||
chr12:26985648
|
A | ATAT | 9 | a0001c0001t0001g0277a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 11 | HG00733.hp2 HG00741.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.869-2790_869-2789i others(5): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985648 | ||||||
chr12:26985648
|
A | T | 5 | a0001c0001t0002g0039a0001c0001t0002g0173a0001c0001t0003g0115others(2): Show | 5 | HG01358.hp1 HG02523.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-2789T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985648 | ||||||
chr12:26985650
|
A | ATAT | 4 | a0001c0001t0002g0170a0001c0001t0002g0341a0001c0001t0002g0345others(1): Show | 4 | HG02004.hp1 HG02300.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2792_869-2791i others(5): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985650 | ||||||
chr12:26985650
|
A | T | 36 | a0001c0001t0001g0277a0001c0001t0002g0023a0001c0001t0002g0024others(33): Show | 38 | HG00558.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.869-2791T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985650 | ||||||
chr12:26985652
|
A | AAAATATA others(5): Show |
2 | a0003c0003t0009g0006a0003c0003t0009g0235 | 4 | HG02451.hp1 HG03516.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2794_869-2793i others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | ||||||
chr12:26985652
|
A | AAATATAT others(4): Show |
1 | a0003c0003t0009g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.869-2794_869-2793i others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | ||||||
chr12:26985652
|
A | ATATATAT others(4): Show |
1 | a0003c0003t0009g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.869-2794_869-2793i others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | ||||||
chr12:26985652
|
A | ATATATAT others(6): Show |
1 | a0003c0003t0009g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.869-2794_869-2793i others(15): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | ||||||
chr12:26985652
|
A | T | 82 | a0001c0001t0001g0203a0001c0001t0001g0274a0001c0001t0001g0277others(79): Show | 86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.869-2793T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | ||||||
chr12:26985652
|
AAT | A | 8 | a0001c0001t0001g0025a0001c0001t0002g0132a0001c0001t0004g0030others(5): Show | 9 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.869-2795_869-2794d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | ||||||
chr12:26985653
|
AT | A | 4 | a0001c0001t0002g0140a0001c0001t0004g0122a0001c0001t0004g0201others(1): Show | 4 | NA18973.hp2 NA18991.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2795delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985653 | ||||||
chr12:26985654
|
T | A | 4 | a0001c0001t0002g0093a0001c0001t0008g0226a0001c0001t0008g0355others(1): Show | 4 | HG03130.hp1 HG03225.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2795A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985654 | ||||||
chr12:26985656
|
T | A | 1 | a0001c0001t0004g0307 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.869-2797A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985656 | ||||||
chr12:26985658
|
T | A | 1 | a0001c0001t0008g0352 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.869-2799A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985658 | ||||||
chr12:26985678
|
T | C | 7 | a0001c0001t0007g0328a0001c0001t0027g0231a0003c0003t0009g0006others(4): Show | 9 | HG02451.hp1 HG02818.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.869-2819A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985678 | ||||||
chr12:26985678
|
T | TATATATA others(5): Show |
1 | a0003c0003t0009g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.869-2820_869-2819i others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985678 | ||||||
chr12:26985678
|
T | TATATATA others(7): Show |
1 | a0003c0003t0009g0232 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.869-2820_869-2819i others(16): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985678 | ||||||
chr12:26985680
|
C | T | 91 | a0001c0001t0001g0101a0001c0001t0001g0112a0001c0001t0001g0243others(88): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.869-2821G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985680 | ||||||
chr12:26985806
|
G | GT | 88 | a0001c0001t0001g0027a0001c0001t0001g0055a0001c0001t0001g0101others(85): Show | 94 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.869-2948dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985806
|
G | GTT | 109 | a0001c0001t0001g0203a0001c0001t0001g0274a0001c0001t0001g0277others(106): Show | 116 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.869-2949_869-2948d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985806
|
G | GTTT | 7 | a0001c0001t0002g0034a0001c0001t0002g0137a0001c0001t0002g0174others(4): Show | 7 | HG00735.hp2 HG00738.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-2950_869-2948d others(5): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985806
|
G | GTTTTT | 7 | a0002c0002t0001g0198a0002c0002t0004g0386a0002c0002t0005g0374others(4): Show | 7 | HG01069.hp1 NA18969.hp1 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-2952_869-2948d others(7): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985806
|
G | GTTTTTT | 18 | a0002c0002t0001g0199a0002c0002t0001g0336a0002c0002t0005g0022others(15): Show | 21 | HG00609.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.869-2953_869-2948d others(8): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985806
|
GT | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(62): Show | 76 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.869-2948delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985806
|
GTT | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(54): Show | 68 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.869-2949_869-2948d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | ||||||
chr12:26985845
|
G | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0096others(13): Show | 18 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.869-2986C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985845 | ||||||
chr12:26985888
|
A | ACTGCCAG | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 166 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.869-3036_869-3030d others(9): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985888 | ||||||
chr12:26985929
|
T | C | 1 | a0001c0001t0003g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.869-3070A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985929 | ||||||
chr12:26985946
|
A | G | 27 | a0001c0001t0004g0118a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-3087T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985946 | ||||||
chr12:26985968
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.869-3109G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985968 | ||||||
chr12:26985981
|
G | A | 2 | a0002c0002t0014g0363a0002c0002t0014g0372 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.869-3122C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985981 | ||||||
chr12:26985998
|
G | GT | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.869-3140dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985998 | ||||||
chr12:26985998
|
G | GTT | 5 | a0001c0001t0013g0017a0001c0001t0013g0261a0001c0001t0013g0262others(2): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-3141_869-3140d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985998 | ||||||
chr12:26986018
|
C | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.869-3159G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986018 | ||||||
chr12:26986029
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.869-3170A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986029 | ||||||
chr12:26986123
|
C | T | 10 | a0001c0001t0015g0078a0001c0001t0015g0079a0001c0001t0027g0231others(7): Show | 12 | HG02257.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.869-3264G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986123 | ||||||
chr12:26986124
|
G | A | 1 | a0001c0001t0019g0276 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.869-3265C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986124 | ||||||
chr12:26986175
|
C | T | 7 | a0003c0003t0009g0006a0003c0003t0009g0232a0003c0003t0009g0233others(4): Show | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.869-3316G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986175 | ||||||
chr12:26986383
|
C | A | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.869-3524G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986383 | ||||||
chr12:26986405
|
C | T | 1 | a0001c0001t0007g0050 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.869-3546G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986405 | ||||||
chr12:26986541
|
C | T | 3 | a0001c0001t0008g0082a0001c0001t0008g0352a0001c0001t0008g0353 | 3 | HG01123.hp2 HG01175.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.869-3682G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986541 | ||||||
chr12:26986618
|
G | A | 4 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(1): Show | 4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3759C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986618 | ||||||
chr12:26986790
|
C | T | 1 | a0001c0001t0004g0201 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.868+3660G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986790 | ||||||
chr12:26986791
|
T | A | 2 | a0001c0001t0026g0150a0001c0001t0028g0151 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.868+3659A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986791 | ||||||
chr12:26986928
|
T | G | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.868+3522A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986928 | ||||||
chr12:26986994
|
C | T | 7 | a0003c0003t0009g0006a0003c0003t0009g0232a0003c0003t0009g0233others(4): Show | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.868+3456G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986994 | ||||||
chr12:26987019
|
T | C | 1 | a0002c0002t0005g0380 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.868+3431A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987019 | ||||||
chr12:26987044
|
G | T | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.868+3406C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987044 | ||||||
chr12:26987054
|
T | A | 26 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.868+3396A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987054 | ||||||
chr12:26987104
|
C | A | 4 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(1): Show | 4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+3346G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987104 | ||||||
chr12:26987335
|
C | A | 1 | a0002c0002t0005g0338 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.868+3115G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987335 | ||||||
chr12:26987426
|
C | A | 7 | a0001c0001t0004g0377a0001c0001t0020g0361a0001c0001t0020g0375others(4): Show | 7 | HG00738.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.868+3024G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987426 | ||||||
chr12:26987593
|
T | C | 2 | a0001c0001t0006g0149a0001c0001t0016g0148 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.868+2857A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987593 | ||||||
chr12:26987616
|
C | T | 6 | a0001c0001t0010g0213a0001c0001t0010g0251a0001c0001t0010g0255others(3): Show | 6 | HG00280.hp2 HG01175.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.868+2834G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987616 | ||||||
chr12:26988062
|
TA | T | 12 | a0001c0001t0001g0209a0001c0001t0003g0095a0001c0001t0004g0212others(9): Show | 12 | HG01256.hp1 HG01993.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.868+2387delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988062 | ||||||
chr12:26988177
|
C | T | 4 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(1): Show | 4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+2273G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988177 | ||||||
chr12:26988212
|
G | C | 33 | a0001c0001t0001g0027a0001c0001t0006g0042a0001c0001t0006g0043others(30): Show | 33 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.868+2238C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988212 | ||||||
chr12:26988231
|
C | T | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.868+2219G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988231 | ||||||
chr12:26988281
|
A | G | 1 | a0001c0001t0006g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.868+2169T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988281 | ||||||
chr12:26988462
|
C | T | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.868+1988G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988462 | ||||||
chr12:26988471
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 162 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.868+1979T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988471 | ||||||
chr12:26988484
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.868+1966A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988484 | ||||||
chr12:26988628
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0189 | 2 | HG02055.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.868+1822A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988628 | ||||||
chr12:26988672
|
T | TTG | 10 | a0001c0001t0001g0271a0001c0001t0002g0345a0001c0001t0004g0329others(7): Show | 10 | HG01256.hp1 HG02004.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+1776_868+1777d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
T | TTGTG | 17 | a0001c0001t0003g0004a0001c0001t0003g0086a0001c0001t0003g0087others(14): Show | 19 | HG00642.hp2 HG01255.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.868+1774_868+1777d others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
T | TTGTGTG | 25 | a0001c0001t0003g0142a0001c0001t0003g0215a0001c0001t0003g0216others(22): Show | 25 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.868+1772_868+1777d others(8): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
T | TTGTGTGT others(1): Show |
50 | a0001c0001t0001g0027a0001c0001t0001g0088a0001c0001t0001g0089others(47): Show | 52 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.868+1770_868+1777d others(10): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
T | TTGTGTGT others(3): Show |
12 | a0001c0001t0002g0107a0001c0001t0002g0141a0001c0001t0003g0045others(9): Show | 12 | HG02129.hp1 HG02257.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.868+1768_868+1777d others(12): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
T | TTGTGTGT others(5): Show |
7 | a0001c0001t0003g0010a0001c0001t0003g0057a0001c0001t0003g0077others(4): Show | 8 | HG00099.hp2 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.868+1766_868+1777d others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0003g0156 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.868+1764_868+1777d others(16): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
TTG | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.868+1776_868+1777d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26988672
|
TTGTG | T | 26 | a0001c0001t0001g0334a0002c0002t0001g0198a0002c0002t0001g0199others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.868+1774_868+1777d others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | ||||||
chr12:26989008
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 159 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.868+1442A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989008 | ||||||
chr12:26989054
|
C | T | 2 | a0001c0001t0008g0082a0001c0001t0008g0352 | 2 | HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.868+1396G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989054 | ||||||
chr12:26989092
|
G | A | 2 | a0001c0001t0003g0154a0001c0001t0016g0092 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.868+1358C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989092 | ||||||
chr12:26989144
|
G | A | 10 | a0001c0001t0002g0014a0001c0001t0002g0166a0001c0001t0002g0174others(7): Show | 11 | NA18941.hp2 NA18942.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.868+1306C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989144 | ||||||
chr12:26989253
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.868+1197A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989253 | ||||||
chr12:26989465
|
G | A | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(334): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.868+985C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989465 | ||||||
chr12:26989668
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 122 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.868+782A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989668 | ||||||
chr12:26989668
|
T | TAC | 61 | a0001c0001t0001g0203a0001c0001t0001g0274a0001c0001t0001g0277others(58): Show | 64 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.868+780_868+781dup others(2): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989668 | ||||||
chr12:26989668
|
T | TACAC | 58 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0135others(55): Show | 61 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.868+778_868+781dup others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989668 | ||||||
chr12:26989898
|
A | G | 1 | a0001c0001t0006g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.868+552T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989898 | ||||||
chr12:26990083
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 284 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.868+367A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26990083 | ||||||
chr12:26990160
|
G | A | 1 | a0001c0001t0002g0376 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.868+290C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26990160 | ||||||
chr12:26990370
|
T | C | 1 | a0001c0001t0006g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.868+80A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26990370 | ||||||
chr12:26990646
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-19G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26990646 | ||||||
chr12:26990646
|
CAT | C | 3 | a0001c0001t0027g0231a0002c0002t0014g0363a0002c0002t0014g0372 | 3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.691-21_691-20delAT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26990646 | ||||||
chr12:26990699
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 126 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.691-72G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26990699 | ||||||
chr12:26991059
|
G | A | 5 | a0001c0001t0003g0057a0001c0001t0014g0081a0001c0001t0015g0078others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-432C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991059 | ||||||
chr12:26991089
|
A | G | 26 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-462T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991089 | ||||||
chr12:26991139
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.691-512A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991139 | ||||||
chr12:26991141
|
C | CT | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 155 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.691-515dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | ||||||
chr12:26991141
|
C | CTT | 12 | a0001c0001t0001g0178a0001c0001t0001g0243a0001c0001t0001g0264others(9): Show | 12 | HG00642.hp1 HG02723.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-516_691-515dup others(2): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | ||||||
chr12:26991141
|
CT | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0271a0001c0001t0002g0038others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-515delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | ||||||
chr12:26991141
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0020g0361a0001c0001t0020g0375a0001c0001t0027g0231others(3): Show | 6 | HG00738.hp1 HG02109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-523_691-515del others(9): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | ||||||
chr12:26991176
|
C | T | 8 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0007g0008others(5): Show | 9 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.691-549G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991176 | ||||||
chr12:26991242
|
T | C | 70 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0096others(67): Show | 75 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.691-615A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991242 | ||||||
chr12:26991253
|
C | T | 3 | a0001c0001t0027g0231a0002c0002t0014g0363a0002c0002t0014g0372 | 3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.691-626G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991253 | ||||||
chr12:26991301
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.691-674G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991301 | ||||||
chr12:26991302
|
G | A | 71 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0096others(68): Show | 76 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.691-675C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991302 | ||||||
chr12:26991320
|
T | C | 26 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-693A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991320 | ||||||
chr12:26991373
|
C | T | 1 | a0001c0001t0027g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-746G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991373 | ||||||
chr12:26991379
|
C | T | 1 | a0001c0001t0017g0331 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.691-752G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991379 | ||||||
chr12:26991418
|
C | CTGGGATT others(4): Show |
1 | a0002c0002t0012g0388 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.691-802_691-792dup others(11): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991418 | ||||||
chr12:26991527
|
C | T | 26 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0336others(23): Show | 29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-900G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991527 | ||||||
chr12:26991629
|
G | A | 2 | a0001c0001t0004g0193a0001c0001t0035g0032 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.691-1002C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991629 | ||||||
chr12:26991793
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.691-1166G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991793 | ||||||
chr12:26991865
|
G | C | 3 | a0001c0001t0018g0126a0001c0001t0018g0127a0001c0001t0018g0128 | 3 | HG02717.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.691-1238C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991865 | ||||||
chr12:26991904
|
C | A | 1 | a0007c0008t0036g0133 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691-1277G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991904 | ||||||
chr12:26991905
|
A | C | 1 | a0007c0008t0036g0133 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691-1278T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991905 | ||||||
chr12:26991906
|
C | A | 1 | a0007c0008t0036g0133 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691-1279G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991906 | ||||||
chr12:26991947
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-1320G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991947 | ||||||
chr12:26992001
|
T | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-1374A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992001 | ||||||
chr12:26992156
|
G | A | 1 | a0001c0001t0004g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.691-1529C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992156 | ||||||
chr12:26992225
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.691-1598C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992225 | ||||||
chr12:26992270
|
T | A | 10 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0006g0048others(7): Show | 11 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-1643A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992270 | ||||||
chr12:26992273
|
A | T | 4 | a0001c0001t0003g0057a0001c0001t0004g0163a0001c0001t0014g0081others(1): Show | 4 | HG02886.hp2 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1646T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992273 | ||||||
chr12:26992364
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(2): Show | 5 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-1737A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992364 | ||||||
chr12:26992428
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.691-1801C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992428 | ||||||
chr12:26992506
|
G | A | 1 | a0001c0001t0004g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.691-1879C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992506 | ||||||
chr12:26992576
|
G | A | 1 | a0001c0001t0005g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.691-1949C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992576 | ||||||
chr12:26992580
|
G | A | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.691-1953C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992580 | ||||||
chr12:26992654
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0002g0054 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.691-2027C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992654 | ||||||
chr12:26992659
|
C | T | 1 | a0001c0001t0020g0361 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.691-2032G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992659 | ||||||
chr12:26992666
|
C | T | 1 | a0001c0001t0006g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.691-2039G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992666 | ||||||
chr12:26992668
|
G | A | 1 | a0001c0001t0006g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.691-2041C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992668 | ||||||
chr12:26992864
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 126 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.691-2237A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992864 | ||||||
chr12:26992905
|
C | CT | 51 | a0001c0001t0001g0203a0001c0001t0001g0227a0001c0001t0001g0238others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.691-2279dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | ||||||
chr12:26992905
|
C | CTT | 71 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0096others(68): Show | 76 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.691-2280_691-2279d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | ||||||
chr12:26992905
|
CT | C | 39 | a0001c0001t0004g0201a0001c0001t0013g0017a0001c0001t0013g0261others(36): Show | 45 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.691-2279delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | ||||||
chr12:26992905
|
CTT | C | 12 | a0001c0001t0004g0377a0001c0001t0015g0080a0001c0001t0017g0225others(9): Show | 12 | HG00738.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-2280_691-2279d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | ||||||
chr12:26992980
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.690+2257C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992980 | ||||||
chr12:26993108
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.690+2129C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993108 | ||||||
chr12:26993509
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(340): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.690+1728T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993509 | ||||||
chr12:26993586
|
C | A | 1 | a0001c0001t0002g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.690+1651G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993586 | ||||||
chr12:26993645
|
C | T | 1 | a0001c0001t0029g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.690+1592G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993645 | ||||||
chr12:26994084
|
T | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.690+1153A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994084 | ||||||
chr12:26994146
|
G | A | 1 | a0001c0001t0004g0324 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.690+1091C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994146 | ||||||
chr12:26994307
|
G | T | 2 | a0002c0002t0014g0363a0002c0002t0014g0372 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.690+930C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994307 | ||||||
chr12:26994422
|
T | C | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.690+815A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994422 | ||||||
chr12:26994578
|
C | T | 1 | a0001c0001t0027g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.690+659G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994578 | ||||||
chr12:26994672
|
C | G | 5 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(2): Show | 5 | HG00738.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+565G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994672 | ||||||
chr12:26994951
|
G | A | 1 | a0001c0001t0010g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.690+286C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994951 | ||||||
chr12:26994967
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+270G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994967 | ||||||
chr12:26995181
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.690+56G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26995181 | ||||||
chr12:26995464
|
TA | T | 5 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(2): Show | 5 | HG00738.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-57delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995464 | ||||||
chr12:26995578
|
T | C | 3 | a0001c0001t0018g0126a0001c0001t0018g0127a0001c0001t0018g0128 | 3 | HG02717.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519-170A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995578 | ||||||
chr12:26995797
|
C | T | 2 | a0001c0001t0003g0057a0001c0001t0014g0081 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.519-389G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995797 | ||||||
chr12:26995930
|
A | T | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.519-522T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995930 | ||||||
chr12:26996008
|
G | A | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.519-600C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996008 | ||||||
chr12:26996016
|
A | T | 1 | a0009c0007t0004g0365 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.519-608T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996016 | ||||||
chr12:26996024
|
T | A | 2 | a0001c0001t0004g0131a0001c0001t0037g0130 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.519-616A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996024 | ||||||
chr12:26996025
|
A | T | 1 | a0001c0001t0002g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.519-617T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996025 | ||||||
chr12:26996153
|
TA | T | 7 | a0001c0001t0003g0194a0001c0001t0005g0223a0001c0001t0017g0331others(4): Show | 7 | HG02723.hp2 HG02897.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+588delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996153 | ||||||
chr12:26996317
|
C | T | 6 | a0001c0001t0010g0213a0001c0001t0010g0251a0001c0001t0010g0255others(3): Show | 6 | HG00280.hp2 HG01175.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+425G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996317 | ||||||
chr12:26996376
|
G | T | 6 | a0001c0001t0002g0029a0001c0001t0002g0035a0001c0001t0002g0036others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+366C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996376 | ||||||
chr12:26996535
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.518+207T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996535 | ||||||
chr12:26996624
|
C | A | 2 | a0002c0002t0014g0363a0002c0002t0014g0372 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.518+118G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996624 | ||||||
chr12:26996973
|
A | G | 4 | a0001c0001t0015g0080a0001c0001t0017g0225a0001c0001t0026g0150others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-111T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26996973 | ||||||
chr12:26996981
|
C | T | 1 | a0001c0001t0002g0343 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.398-119G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26996981 | ||||||
chr12:26997095
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-233A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997095 | ||||||
chr12:26997177
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 143 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.398-315T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997177 | ||||||
chr12:26997330
|
G | A | 1 | a0001c0001t0003g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.398-468C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997330 | ||||||
chr12:26997479
|
T | C | 1 | a0001c0001t0004g0122 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.398-617A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997479 | ||||||
chr12:26997481
|
T | C | 3 | a0001c0001t0006g0066a0001c0001t0006g0067a0001c0001t0006g0068 | 3 | HG03669.hp2 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.398-619A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997481 | ||||||
chr12:26997546
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 129 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.398-684C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997546 | ||||||
chr12:26997823
|
C | CT | 18 | a0001c0001t0001g0009a0001c0001t0003g0011a0001c0001t0003g0012others(15): Show | 21 | HG00544.hp1 HG00673.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.398-962dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997823 | ||||||
chr12:26997823
|
C | CTTT | 85 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0073others(82): Show | 92 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.398-964_398-962dup others(3): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997823 | ||||||
chr12:26997823
|
CT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.398-962delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997823 | ||||||
chr12:26997853
|
TCTTGCTC others(11): Show |
T | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.398-1009_398-992de others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997853 | ||||||
chr12:26997940
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.398-1078G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997940 | ||||||
chr12:26997984
|
CCTGA | C | 21 | a0001c0001t0003g0119a0001c0001t0004g0005a0001c0001t0004g0013others(18): Show | 24 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.398-1126_398-1123d others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997984 | ||||||
chr12:26998123
|
G | A | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.398-1261C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998123 | ||||||
chr12:26998385
|
C | T | 1 | a0001c0001t0004g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.397+1141G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998385 | ||||||
chr12:26998457
|
G | A | 3 | a0001c0001t0027g0231a0002c0002t0014g0363a0002c0002t0014g0372 | 3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.397+1069C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998457 | ||||||
chr12:26998747
|
A | G | 130 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0088others(127): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.397+779T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998747 | ||||||
chr12:26998856
|
G | T | 1 | a0001c0001t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.397+670C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998856 | ||||||
chr12:26998888
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.397+638G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998888 | ||||||
chr12:26998958
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.397+568G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998958 | ||||||
chr12:26999338
|
G | C | 1 | a0001c0001t0004g0325 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.397+188C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999338 | ||||||
chr12:26999395
|
C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(115): Show | 139 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.397+130dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999395 | ||||||
chr12:26999395
|
CA | C | 21 | a0001c0001t0001g0027a0001c0001t0006g0042a0001c0001t0006g0043others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.397+130delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999395 | ||||||
chr12:26999411
|
G | A | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+115C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999411 | ||||||
chr12:26999446
|
A | G | 3 | a0001c0001t0027g0231a0002c0002t0014g0363a0002c0002t0014g0372 | 3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.397+80T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999446 | ||||||
chr12:26999733
|
T | C | 370 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(367): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.247-57A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999733 | ||||||
chr12:26999742
|
C | T | 1 | a0001c0001t0007g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.247-66G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999742 | ||||||
chr12:26999751
|
A | G | 4 | a0001c0001t0003g0057a0001c0001t0014g0081a0001c0001t0015g0078others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-75T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999751 | ||||||
chr12:26999794
|
C | A | 1 | a0001c0001t0001g0267 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.247-118G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999794 | ||||||
chr12:26999894
|
T | G | 4 | a0001c0001t0001g0112a0001c0001t0005g0113a0001c0001t0005g0153others(1): Show | 4 | HG00597.hp1 NA19058.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-218A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999894 | ||||||
chr12:27000056
|
C | T | 3 | a0001c0001t0027g0231a0002c0002t0014g0363a0002c0002t0014g0372 | 3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.247-380G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000056 | ||||||
chr12:27000101
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.247-425A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000101 | ||||||
chr12:27000142
|
G | A | 1 | a0001c0001t0008g0357 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.247-466C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000142 | ||||||
chr12:27000255
|
C | G | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.247-579G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000255 | ||||||
chr12:27000307
|
T | C | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247-631A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000307 | ||||||
chr12:27000522
|
C | T | 4 | a0001c0001t0015g0080a0001c0001t0017g0225a0001c0001t0026g0150others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-846G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000522 | ||||||
chr12:27000567
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.247-891G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000567 | ||||||
chr12:27000584
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-908G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000584 | ||||||
chr12:27000585
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-909T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000585 | ||||||
chr12:27000597
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.247-921G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000597 | ||||||
chr12:27000600
|
C | T | 21 | a0001c0001t0003g0119a0001c0001t0004g0005a0001c0001t0004g0013others(18): Show | 24 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-924G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000600 | ||||||
chr12:27000650
|
G | A | 1 | a0001c0001t0003g0114 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.247-974C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000650 | ||||||
chr12:27000701
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.247-1025G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000701 | ||||||
chr12:27000739
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.247-1063C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000739 | ||||||
chr12:27000785
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0288a0001c0001t0005g0287others(5): Show | 9 | HG02135.hp1 HG02165.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-1109T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000785 | ||||||
chr12:27000821
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.247-1145A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000821 | ||||||
chr12:27000835
|
A | C | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247-1159T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000835 | ||||||
chr12:27000857
|
C | T | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.247-1181G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000857 | ||||||
chr12:27001197
|
G | A | 21 | a0001c0001t0001g0027a0001c0001t0006g0042a0001c0001t0006g0043others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.247-1521C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001197 | ||||||
chr12:27001238
|
G | T | 64 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0089others(61): Show | 70 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.247-1562C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001238 | ||||||
chr12:27001437
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.247-1761G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001437 | ||||||
chr12:27001609
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.246+1627G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001609 | ||||||
chr12:27001679
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.246+1557G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001679 | ||||||
chr12:27001726
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.246+1510T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001726 | ||||||
chr12:27001812
|
C | A | 2 | a0001c0001t0003g0057a0001c0001t0014g0081 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.246+1424G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001812 | ||||||
chr12:27001891
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.246+1345G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001891 | ||||||
chr12:27001938
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.246+1298C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001938 | ||||||
chr12:27002037
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.246+1199A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002037 | ||||||
chr12:27002117
|
G | A | 8 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0007g0008others(5): Show | 9 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+1119C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002117 | ||||||
chr12:27002187
|
G | T | 1 | a0001c0001t0027g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.246+1049C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002187 | ||||||
chr12:27002235
|
G | A | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.246+1001C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002235 | ||||||
chr12:27002237
|
C | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.246+999G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002237 | ||||||
chr12:27002297
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.246+939A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002297 | ||||||
chr12:27002299
|
C | CA | 183 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0044others(180): Show | 198 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.246+936dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002299 | ||||||
chr12:27002352
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 129 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.246+884G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002352 | ||||||
chr12:27002454
|
T | A | 1 | a0002c0002t0005g0382 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.246+782A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002454 | ||||||
chr12:27002630
|
G | C | 1 | a0001c0001t0006g0028 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.246+606C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002630 | ||||||
chr12:27002709
|
T | C | 5 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(2): Show | 5 | HG00738.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+527A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002709 | ||||||
chr12:27003095
|
T | C | 1 | a0001c0001t0006g0043 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.246+141A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003095 | ||||||
chr12:27003111
|
T | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 139 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.246+125A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003111 | ||||||
chr12:27003143
|
A | G | 1 | a0002c0002t0005g0382 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.246+93T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003143 | ||||||
chr12:27003180
|
T | TACCAGAC others(4): Show |
1 | a0002c0002t0005g0382 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.246+45_246+55dupGG others(9): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003180 | ||||||
chr12:27003609
|
T | C | 1 | a0001c0001t0004g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.92-219A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003609 | ||||||
chr12:27003713
|
G | C | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-323C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003713 | ||||||
chr12:27003783
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.92-393C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003783 | ||||||
chr12:27003803
|
A | G | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-413T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003803 | ||||||
chr12:27003859
|
T | C | 1 | a0001c0001t0006g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-469A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003859 | ||||||
chr12:27004153
|
T | A | 1 | a0001c0001t0008g0350 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92-763A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004153 | ||||||
chr12:27004260
|
C | A | 1 | a0002c0002t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.92-870G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004260 | ||||||
chr12:27004285
|
C | G | 1 | a0001c0001t0002g0340 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.92-895G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004285 | ||||||
chr12:27004589
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.92-1199C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004589 | ||||||
chr12:27004671
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 133 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.92-1281T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004671 | ||||||
chr12:27004964
|
G | A | 4 | a0001c0001t0006g0147a0001c0001t0027g0231a0002c0002t0014g0363others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-1574C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004964 | ||||||
chr12:27004964
|
G | T | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-1574C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004964 | ||||||
chr12:27005173
|
C | A | 1 | a0001c0001t0029g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.92-1783G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005173 | ||||||
chr12:27005223
|
A | T | 12 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0004g0131others(9): Show | 13 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-1833T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005223 | ||||||
chr12:27005347
|
T | C | 7 | a0001c0001t0003g0045a0001c0001t0003g0057a0001c0001t0003g0076others(4): Show | 7 | HG00738.hp1 HG02257.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-1957A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005347 | ||||||
chr12:27005355
|
A | G | 1 | a0004c0004t0016g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-1965T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005355 | ||||||
chr12:27005356
|
C | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG00642.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.92-1966G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005356 | ||||||
chr12:27005405
|
C | A | 1 | a0001c0001t0004g0327 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.92-2015G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005405 | ||||||
chr12:27005506
|
T | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0089others(72): Show | 81 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.92-2116A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005506 | ||||||
chr12:27005555
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 83 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.92-2165G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005555 | ||||||
chr12:27005561
|
A | G | 2 | a0002c0002t0014g0363a0002c0002t0014g0372 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-2171T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005561 | ||||||
chr12:27005764
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.92-2374C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005764 | ||||||
chr12:27005788
|
G | C | 12 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0004g0131others(9): Show | 13 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-2398C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005788 | ||||||
chr12:27005804
|
A | AT | 6 | a0001c0001t0001g0116a0001c0001t0003g0057a0001c0001t0004g0298others(3): Show | 6 | HG02886.hp2 HG03453.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-2415dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005804 | ||||||
chr12:27005877
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.92-2487A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005877 | ||||||
chr12:27005958
|
C | T | 1 | a0001c0001t0008g0350 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92-2568G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005958 | ||||||
chr12:27005989
|
G | A | 3 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0005g0197 | 3 | HG00609.hp2 NA18969.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.92-2599C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005989 | ||||||
chr12:27006015
|
G | T | 71 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0089others(68): Show | 77 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.92-2625C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006015 | ||||||
chr12:27006019
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.92-2629G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006019 | ||||||
chr12:27006029
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 143 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.92-2639T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006029 | ||||||
chr12:27006096
|
G | A | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.92-2706C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006096 | ||||||
chr12:27006140
|
C | CT | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0027others(21): Show | 26 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-2751dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006140 | ||||||
chr12:27006144
|
T | C | 5 | a0001c0001t0006g0147a0001c0001t0006g0149a0001c0001t0027g0231others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-2754A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006144 | ||||||
chr12:27006146
|
T | C | 6 | a0001c0001t0003g0045a0001c0001t0003g0076a0001c0001t0003g0077others(3): Show | 6 | HG00738.hp1 HG02132.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-2756A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006146 | ||||||
chr12:27006178
|
C | T | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.92-2788G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006178 | ||||||
chr12:27006200
|
G | A | 27 | a0001c0001t0035g0032a0002c0002t0001g0198a0002c0002t0001g0199others(24): Show | 30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-2810C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006200 | ||||||
chr12:27006284
|
T | G | 1 | a0001c0001t0003g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.92-2894A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006284 | ||||||
chr12:27006372
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0279a0001c0001t0001g0280others(7): Show | 11 | HG00597.hp2 HG01257.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-2982G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006372 | ||||||
chr12:27006415
|
G | A | 1 | a0001c0001t0017g0331 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.92-3025C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006415 | ||||||
chr12:27006490
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.92-3100C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006490 | ||||||
chr12:27006493
|
C | T | 2 | a0001c0001t0003g0057a0001c0001t0014g0081 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-3103G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006493 | ||||||
chr12:27006545
|
T | C | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.92-3155A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006545 | ||||||
chr12:27006701
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.92-3311C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006701 | ||||||
chr12:27006796
|
A | G | 27 | a0001c0001t0001g0027a0001c0001t0006g0042a0001c0001t0006g0043others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-3406T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006796 | ||||||
chr12:27006851
|
A | G | 54 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0001t0004g0131others(51): Show | 60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.92-3461T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006851 | ||||||
chr12:27007028
|
T | C | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.92-3638A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007028 | ||||||
chr12:27007243
|
C | T | 3 | a0001c0001t0010g0251a0004c0004t0010g0252a0004c0004t0010g0253 | 3 | HG02486.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.92-3853G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007243 | ||||||
chr12:27007278
|
C | G | 1 | a0001c0001t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.92-3888G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007278 | ||||||
chr12:27007350
|
A | G | 3 | a0001c0001t0006g0147a0001c0001t0006g0149a0001c0001t0027g0231 | 3 | HG02559.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.92-3960T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007350 | ||||||
chr12:27007422
|
C | T | 64 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0089others(61): Show | 70 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.92-4032G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007422 | ||||||
chr12:27007461
|
T | C | 2 | a0001c0001t0015g0080a0001c0001t0017g0225 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.92-4071A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007461 | ||||||
chr12:27007535
|
A | T | 1 | a0001c0001t0001g0272 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.92-4145T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007535 | ||||||
chr12:27007729
|
G | A | 30 | a0001c0001t0001g0027a0001c0001t0001g0046a0001c0001t0001g0071others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-4339C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007729 | ||||||
chr12:27007800
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-4410A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007800 | ||||||
chr12:27007897
|
T | A | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.92-4507A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007897 | ||||||
chr12:27008073
|
CTGTGAGT others(1351): Show |
C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4647_92-4684del | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008073 | ||||||
chr12:27008196
|
G | A | 32 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0340others(29): Show | 36 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-4806C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008196 | ||||||
chr12:27008262
|
T | C | 2 | a0002c0002t0014g0363a0002c0002t0014g0372 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-4872A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008262 | ||||||
chr12:27008269
|
C | T | 46 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0029others(43): Show | 50 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-4879G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008269 | ||||||
chr12:27008446
|
C | T | 46 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0029others(43): Show | 50 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-5056G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008446 | ||||||
chr12:27008592
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 185 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.92-5202A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008592 | ||||||
chr12:27008670
|
C | T | 1 | a0001c0001t0005g0153 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.92-5280G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008670 | ||||||
chr12:27008695
|
G | A | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.92-5305C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008695 | ||||||
chr12:27008975
|
C | T | 45 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0029others(42): Show | 49 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.91+5103G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008975 | ||||||
chr12:27009055
|
T | C | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+5023A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009055 | ||||||
chr12:27009122
|
CTTAT | C | 2 | a0001c0001t0003g0211a0002c0002t0012g0016 | 3 | NA18982.hp2 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.91+4952_91+4955del others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009122 | ||||||
chr12:27009161
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+4917T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009161 | ||||||
chr12:27009270
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0008g0033 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.91+4808T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009270 | ||||||
chr12:27009285
|
C | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(86): Show | 99 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.91+4793G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009285 | ||||||
chr12:27009287
|
A | C | 14 | a0001c0001t0002g0029a0001c0001t0002g0034a0001c0001t0002g0035others(11): Show | 14 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+4791T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009287 | ||||||
chr12:27009343
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(313): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.91+4735T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009343 | ||||||
chr12:27009401
|
G | A | 2 | a0002c0002t0014g0363a0002c0002t0014g0372 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.91+4677C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009401 | ||||||
chr12:27009432
|
T | C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4646A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009432 | ||||||
chr12:27009434
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4644A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009434 | ||||||
chr12:27009436
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4642A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009436 | ||||||
chr12:27009442
|
A | C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4636T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009442 | ||||||
chr12:27009443
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4635A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009443 | ||||||
chr12:27009444
|
G | GCAC | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4633_91+4634ins others(3): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009444 | ||||||
chr12:27009447
|
GA | G | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4630delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009447 | ||||||
chr12:27009449
|
G | C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4629C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009449 | ||||||
chr12:27009451
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4627A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009451 | ||||||
chr12:27009452
|
G | C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4626C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009452 | ||||||
chr12:27009455
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4623A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009455 | ||||||
chr12:27009456
|
T | C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4622A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009456 | ||||||
chr12:27009457
|
A | C | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4621T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009457 | ||||||
chr12:27009458
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4620A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009458 | ||||||
chr12:27009460
|
T | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4618A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009460 | ||||||
chr12:27009461
|
T | G | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4617A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009461 | ||||||
chr12:27009464
|
T | G | 4 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0129others(1): Show | 6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4614A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009464 | ||||||
chr12:27009539
|
T | C | 2 | a0001c0001t0004g0131a0001c0001t0037g0130 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.91+4539A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009539 | ||||||
chr12:27009651
|
A | G | 1 | a0001c0001t0005g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.91+4427T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009651 | ||||||
chr12:27009679
|
G | A | 1 | a0001c0001t0006g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.91+4399C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009679 | ||||||
chr12:27009839
|
T | G | 2 | a0001c0001t0026g0150a0001c0001t0028g0151 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.91+4239A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009839 | ||||||
chr12:27009842
|
A | AT | 45 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0029others(42): Show | 49 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.91+4235dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009842 | ||||||
chr12:27009901
|
T | C | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+4177A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009901 | ||||||
chr12:27010157
|
A | T | 2 | a0001c0001t0007g0239a0001c0001t0007g0240 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.91+3921T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010157 | ||||||
chr12:27010303
|
A | C | 1 | a0001c0001t0001g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.91+3775T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010303 | ||||||
chr12:27010332
|
C | T | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+3746G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010332 | ||||||
chr12:27010341
|
T | C | 1 | a0001c0001t0001g0334 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.91+3737A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010341 | ||||||
chr12:27010410
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 156 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.91+3668A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010410 | ||||||
chr12:27010426
|
C | T | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+3652G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010426 | ||||||
chr12:27010533
|
C | T | 4 | a0001c0001t0003g0194a0001c0001t0004g0196a0001c0001t0004g0207others(1): Show | 4 | NA18946.hp1 NA18961.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+3545G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010533 | ||||||
chr12:27011159
|
C | T | 1 | a0001c0001t0004g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.91+2919G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011159 | ||||||
chr12:27011275
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.91+2803G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011275 | ||||||
chr12:27011316
|
C | T | 1 | a0001c0001t0015g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+2762G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011316 | ||||||
chr12:27011317
|
G | A | 33 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0340others(30): Show | 37 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.91+2761C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011317 | ||||||
chr12:27011786
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+2292G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011786 | ||||||
chr12:27012075
|
T | G | 2 | a0001c0001t0006g0149a0001c0001t0007g0206 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.91+2003A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012075 | ||||||
chr12:27012088
|
G | A | 9 | a0001c0001t0006g0230a0001c0001t0027g0231a0003c0003t0009g0006others(6): Show | 11 | HG00741.hp1 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1990C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012088 | ||||||
chr12:27012162
|
G | A | 2 | a0001c0001t0011g0348a0001c0001t0011g0349 | 2 | NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.91+1916C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012162 | ||||||
chr12:27012170
|
T | C | 4 | a0001c0001t0003g0004a0001c0001t0003g0142a0001c0001t0003g0143others(1): Show | 6 | NA18945.hp2 NA18948.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+1908A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012170 | ||||||
chr12:27012205
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 174 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.91+1873A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012205 | ||||||
chr12:27012231
|
C | T | 3 | a0002c0002t0005g0026a0002c0002t0005g0373a0002c0002t0005g0374 | 4 | HG01069.hp1 HG01071.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+1847G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012231 | ||||||
chr12:27012249
|
G | A | 2 | a0001c0001t0015g0078a0001c0001t0015g0079 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.91+1829C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012249 | ||||||
chr12:27012264
|
A | C | 349 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(346): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.91+1814T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012264 | ||||||
chr12:27012270
|
T | C | 8 | a0001c0001t0003g0194a0001c0001t0004g0196a0001c0001t0004g0207others(5): Show | 8 | HG00609.hp2 NA18946.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+1808A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012270 | ||||||
chr12:27012297
|
C | T | 1 | a0001c0001t0004g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.91+1781G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012297 | ||||||
chr12:27012299
|
C | A | 2 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | NA18961.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.91+1779G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012299 | ||||||
chr12:27012338
|
T | A | 1 | a0001c0001t0005g0360 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.91+1740A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012338 | ||||||
chr12:27012343
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91+1735G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012343 | ||||||
chr12:27012358
|
G | C | 30 | a0001c0001t0002g0029a0001c0001t0002g0034a0001c0001t0002g0035others(27): Show | 31 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+1720C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012358 | ||||||
chr12:27012449
|
T | C | 2 | a0001c0001t0020g0361a0001c0001t0020g0375 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.91+1629A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012449 | ||||||
chr12:27012566
|
A | C | 1 | a0001c0001t0010g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.91+1512T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012566 | ||||||
chr12:27012751
|
G | A | 74 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0089others(71): Show | 80 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.91+1327C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012751 | ||||||
chr12:27012810
|
C | T | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(3): Show | 7 | HG02155.hp1 NA18946.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+1268G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012810 | ||||||
chr12:27012965
|
T | C | 4 | a0001c0001t0006g0149a0001c0001t0016g0148a0001c0001t0026g0150others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+1113A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012965 | ||||||
chr12:27012988
|
A | T | 37 | a0001c0001t0002g0029a0001c0001t0002g0034a0001c0001t0002g0035others(34): Show | 38 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.91+1090T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012988 | ||||||
chr12:27012994
|
T | C | 1 | a0001c0001t0008g0362 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.91+1084A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012994 | ||||||
chr12:27012995
|
C | CA | 124 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0044others(121): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.91+1082dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | ||||||
chr12:27012995
|
C | CAA | 35 | a0001c0001t0002g0029a0001c0001t0002g0034a0001c0001t0002g0035others(32): Show | 36 | HG00597.hp1 HG00639.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+1081_91+1082dup others(2): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | ||||||
chr12:27012995
|
C | CAAA | 51 | a0001c0001t0001g0015a0001c0001t0001g0157a0001c0001t0001g0178others(48): Show | 56 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+1080_91+1082dup others(3): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | ||||||
chr12:27012995
|
C | CAAAA | 8 | a0001c0001t0001g0203a0001c0001t0002g0202a0001c0001t0002g0204others(5): Show | 8 | HG01106.hp2 HG01981.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+1079_91+1082dup others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | ||||||
chr12:27013087
|
A | C | 2 | a0001c0001t0001g0044a0001c0001t0003g0045 | 2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.91+991T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013087 | ||||||
chr12:27013225
|
A | C | 2 | a0001c0001t0006g0042a0001c0001t0006g0043 | 2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.91+853T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013225 | ||||||
chr12:27013289
|
C | A | 1 | a0001c0001t0004g0377 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+789G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013289 | ||||||
chr12:27013642
|
C | T | 177 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0027others(174): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.91+436G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013642 | ||||||
chr12:27013743
|
T | C | 12 | a0002c0002t0004g0386a0002c0002t0005g0378a0002c0002t0005g0379others(9): Show | 12 | HG02135.hp2 NA18956.hp2 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+335A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013743 | ||||||
chr12:27013763
|
C | T | 14 | a0001c0001t0002g0029a0001c0001t0002g0034a0001c0001t0002g0035others(11): Show | 14 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+315G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013763 | ||||||
chr12:27014021
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.91+57G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27014021 |