geneid | 2960 |
---|---|
ensemblid | ENSG00000153767.10 |
hgncid | 4650 |
symbol | GTF2E1 |
name | general transcription factor IIE subunit 1 |
refseq_nuc | NM_005513.3 |
refseq_prot | NP_005504.2 |
ensembl_nuc | ENST00000283875.6 |
ensembl_prot | ENSP00000283875.5 |
mane_status | MANE Select |
chr | chr3 |
start | 120742744 |
end | 120783069 |
strand | + |
ver | v1.2 |
region | chr3:120742744-120783069 |
region5000 | chr3:120737744-120788069 |
regionname0 | GTF2E1_chr3_120742744_120783069 |
regionname5000 | GTF2E1_chr3_120737744_120788069 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 439 | 284 | 77 | 55 | 99 | 14 | 37 | 76 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0002 | 0/0 | 439 | 84 | 0 | 17 | 65 | 0 | 2 | 52 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0003 | 0/0 | 439 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0004 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0005 | 0/0 | 439 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0006 | 0/0 | 439 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0007 | 0/0 | 439 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1320 | 283 | 76 | 55 | 99 | 14 | 37 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0002 | 0/0 | 1320 | 84 | 0 | 17 | 65 | 0 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0003 | 0/0 | 1320 | 4 | 3 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0004 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0005 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0006 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0007 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
c0008 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1681 | 156 | 37 | 27 | 55 | 7 | 28 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0002 | 0/0 | 1682 | 112 | 27 | 19 | 64 | 0 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0003 | 0/0 | 1681 | 80 | 3 | 24 | 36 | 7 | 10 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0004 | 0/0 | 1681 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0005 | 0/0 | 1681 | 4 | 3 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0006 | 0/0 | 1681 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0007 | 0/0 | 1682 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0008 | 0/0 | 1681 | 2 | 1 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0009 | 0/0 | 1681 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0010 | 0/0 | 1682 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0011 | 0/0 | 1681 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0012 | 0/0 | 1681 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0013 | 0/0 | 1681 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0014 | 0/0 | 1682 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0015 | 0/0 | 1681 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0016 | 0/0 | 1682 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
t0017 | 0/0 | 1681 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 23 | 0 | 5 | 17 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0002 | 0/0 | 19 | 0 | 0 | 17 | 0 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0003 | 0/0 | 17 | 1 | 0 | 16 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0004 | 0/0 | 16 | 2 | 6 | 0 | 4 | 4 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0005 | 0/0 | 13 | 0 | 3 | 10 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0006 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0008 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0009 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0011 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0013 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0015 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0041 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1320 | 283 | 76 | 55 | 99 | 14 | 37 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0006 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0002c0002 | 0/0 | 1320 | 84 | 0 | 17 | 65 | 0 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0003c0003 | 0/0 | 1320 | 4 | 3 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0004c0008 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0005c0005 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0006c0007 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0007c0004 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3000 | 150 | 34 | 27 | 53 | 7 | 27 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0002 | 0/0 | 3001 | 30 | 27 | 2 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0003 | 0/0 | 3000 | 79 | 3 | 23 | 36 | 7 | 10 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0004 | 0/0 | 3000 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0006 | 0/0 | 3000 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0007 | 0/0 | 3001 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0008 | 0/0 | 3000 | 2 | 1 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0009 | 0/0 | 3000 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0010 | 0/0 | 3001 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0011 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0012 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0013 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0014 | 0/0 | 3001 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0015 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0016 | 0/0 | 3001 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0001t0017 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0001c0006t0001 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0002c0002t0001 | 0/0 | 3000 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0002c0002t0002 | 0/0 | 3001 | 82 | 0 | 17 | 63 | 0 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0003c0003t0005 | 0/0 | 3000 | 4 | 3 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0004c0008t0003 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0005c0005t0001 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0006c0007t0001 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
a0007c0004t0001 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | copy fasta | chr3 | 120737744 | 120788069 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 16 | 1 | 0 | 15 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0004 | 0/0 | 15 | 2 | 5 | 0 | 4 | 4 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0041 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0002 | 0/0 | 15 | 0 | 0 | 13 | 0 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0013 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0015 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0004g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0004g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0006g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0007g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0010g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0013g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0015g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0016g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0001t0017g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0001 | 0/0 | 23 | 0 | 5 | 17 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0005 | 0/0 | 13 | 0 | 3 | 10 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0009 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0003c0003t0005g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0003c0003t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0004c0008t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0005c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0006c0007t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
a0007c0004t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0144 | EUR | GBR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | GBR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0048 | EUR | GBR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0192 | EUR | FIN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00639 | hp1 | a0001 | c0001 | t0008 | g0157 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | CHS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00738 | hp1 | a0004 | c0008 | t0003 | g0190 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00738 | hp2 | a0001 | c0001 | t0015 | g0004 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01243 | hp1 | a0003 | c0003 | t0005 | g0018 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01433 | hp1 | a0001 | c0001 | t0016 | g0029 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0046 | EUR | IBS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0046 | EUR | IBS | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0164 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0002 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02055 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02145 | hp2 | a0005 | c0005 | t0001 | g0081 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | CDX | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | CDX | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02280 | hp2 | a0003 | c0003 | t0005 | g0018 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0079 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02572 | hp1 | a0001 | c0006 | t0001 | g0094 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02602 | hp1 | a0007 | c0004 | t0001 | g0006 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0182 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02809 | hp1 | a0006 | c0007 | t0001 | g0119 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02922 | hp2 | a0003 | c0003 | t0005 | g0018 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03195 | hp1 | a0001 | c0001 | t0017 | g0189 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03209 | hp1 | a0003 | c0003 | t0005 | g0071 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | CHB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18941 | hp2 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18966 | hp2 | a0001 | c0001 | t0013 | g0014 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18986 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | LWK | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | LWK | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | ASW | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | GIH | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | USA | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | USA | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | LWK | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0041 | REF | REF | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0085 | REF | REF | GTF2E1_chr3_120737744_120788069 | GTF2E1 | chr3 | 120737744 | 120788069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120750575
|
C | T | 1 | a0004 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.23C>T | p.Thr8Ile | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/5 | 104/3000 | 23/1320 | 8/439 | chr3 | 120750575 | ||
chr3:120750819
|
T | A | 1 | a0007 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.267T>A | p.His89Gln | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/5 | 348/3000 | 267/1320 | 89/439 | chr3 | 120750819 | ||
chr3:120750920
|
A | G | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.368A>G | p.Asn123Ser | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/5 | 449/3000 | 368/1320 | 123/439 | chr3 | 120750920 | ||
chr3:120781246
|
C | T | 1 | a0002 | 84 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
missense_variant | MODERATE | c.1096C>T | p.Pro366Ser | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1177/3000 | 1096/1320 | 366/439 | chr3 | 120781246 | ||
chr3:120781252
|
C | T | 1 | a0005 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1102C>T | p.Arg368Cys | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1183/3000 | 1102/1320 | 368/439 | chr3 | 120781252 | ||
chr3:120781256
|
C | T | 1 | a0003 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.1106C>T | p.Pro369Leu | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1187/3000 | 1106/1320 | 369/439 | chr3 | 120781256 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120781218
|
C | T | 1 | a0001c0006 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1068C>T | p.Ser356Ser | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1149/3000 | 1068/1320 | 356/439 | chr3 | 120781218 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120742751
|
G | T | 2 | a0001c0001t0010a0001c0001t0017 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-74G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/5 | 7802 | chr3 | 120742751 | |||||
chr3:120781599
|
T | A | 11 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(8): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*129T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 129 | chr3 | 120781599 | |||||
chr3:120781643
|
A | G | 1 | a0001c0001t0009 | 2 | HG03453.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*173A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 173 | chr3 | 120781643 | |||||
chr3:120781669
|
T | G | 1 | a0003c0003t0005 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*199T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 199 | chr3 | 120781669 | |||||
chr3:120781715
|
C | CT | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(3): Show | 119 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*261dupT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 262 | INFO_REALIGN_3_PRIME | chr3 | 120781715 | ||||
chr3:120781719
|
T | C | 1 | a0001c0001t0011 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 249 | chr3 | 120781719 | |||||
chr3:120781737
|
T | C | 4 | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(1): Show | 9 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*267T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 267 | chr3 | 120781737 | |||||
chr3:120781784
|
C | T | 1 | a0001c0001t0006 | 3 | NA18986.hp1 NA19056.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*314C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 314 | chr3 | 120781784 | |||||
chr3:120781790
|
A | G | 1 | a0001c0001t0010 | 2 | HG02055.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 320 | chr3 | 120781790 | |||||
chr3:120781872
|
T | C | 11 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(8): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*402T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 402 | chr3 | 120781872 | |||||
chr3:120782098
|
G | T | 1 | a0003c0003t0005 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*628G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 628 | chr3 | 120782098 | |||||
chr3:120782317
|
T | C | 1 | a0001c0001t0004 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*847T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 847 | chr3 | 120782317 | |||||
chr3:120782326
|
C | T | 1 | a0001c0001t0016 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 856 | chr3 | 120782326 | |||||
chr3:120782347
|
A | G | 1 | a0001c0001t0013 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*877A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 877 | chr3 | 120782347 | |||||
chr3:120782400
|
A | G | 1 | a0001c0001t0007 | 3 | NA18984.hp2 NA18991.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 930 | chr3 | 120782400 | |||||
chr3:120782533
|
C | T | 1 | a0001c0001t0015 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1063C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1063 | chr3 | 120782533 | |||||
chr3:120782715
|
C | T | 3 | a0001c0001t0004a0001c0001t0010a0001c0001t0017 | 8 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1245C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1245 | chr3 | 120782715 | |||||
chr3:120782783
|
A | G | 2 | a0001c0001t0008a0001c0001t0009 | 4 | HG00639.hp1 HG03195.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1313A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 5/5 | 1313 | chr3 | 120782783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120742872
|
C | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG00280.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-31+78C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120742872 | ||||||
chr3:120742936
|
A | G | 1 | a0002c0002t0002g0009 | 6 | HG00639.hp2 HG01081.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+142A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120742936 | ||||||
chr3:120743183
|
A | G | 1 | a0004c0008t0003g0190 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-31+389A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120743183 | ||||||
chr3:120743393
|
A | G | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-31+599A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120743393 | ||||||
chr3:120743477
|
T | C | 27 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0072others(24): Show | 35 | HG00558.hp1 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-31+683T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120743477 | ||||||
chr3:120744003
|
C | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+1209C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744003 | ||||||
chr3:120744032
|
A | G | 1 | a0001c0001t0004g0055 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-31+1238A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744032 | ||||||
chr3:120744173
|
A | G | 2 | a0002c0002t0002g0186a0002c0002t0002g0187 | 2 | NA18999.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-31+1379A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744173 | ||||||
chr3:120744621
|
A | G | 1 | a0002c0002t0002g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-31+1827A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744621 | ||||||
chr3:120744656
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-31+1862G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744656 | ||||||
chr3:120744894
|
A | T | 1 | a0001c0001t0003g0192 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-31+2100A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744894 | ||||||
chr3:120744919
|
A | G | 1 | a0002c0002t0002g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-31+2125A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744919 | ||||||
chr3:120744927
|
C | CT | 32 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(29): Show | 81 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-31+2146dupT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 120744927 | |||||
chr3:120744990
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-31+2196C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120744990 | ||||||
chr3:120745124
|
A | G | 1 | a0001c0001t0011g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-31+2330A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745124 | ||||||
chr3:120745193
|
T | A | 1 | a0003c0003t0005g0018 | 3 | HG01243.hp1 HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-31+2399T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745193 | ||||||
chr3:120745257
|
G | C | 3 | a0001c0001t0002g0028a0001c0001t0002g0057a0001c0001t0002g0058 | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+2463G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745257 | ||||||
chr3:120745325
|
A | G | 1 | a0001c0001t0004g0055 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-31+2531A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745325 | ||||||
chr3:120745393
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-31+2599A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745393 | ||||||
chr3:120745645
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-31+2851C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745645 | ||||||
chr3:120745810
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-31+3016G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745810 | ||||||
chr3:120745813
|
C | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(13): Show | 22 | HG00639.hp1 HG00735.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31+3019C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745813 | ||||||
chr3:120745819
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-31+3025G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745819 | ||||||
chr3:120745984
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-31+3190C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120745984 | ||||||
chr3:120746052
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 8 | HG00544.hp1 HG01175.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+3258G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746052 | ||||||
chr3:120746279
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-31+3485A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746279 | ||||||
chr3:120746437
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-31+3643C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746437 | ||||||
chr3:120746489
|
C | CA | 10 | a0001c0001t0001g0080a0001c0001t0002g0028a0001c0001t0002g0029others(7): Show | 12 | HG01106.hp1 HG01192.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+3709dupA | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 120746489 | |||||
chr3:120746489
|
C | CAA | 8 | a0001c0001t0001g0016a0001c0001t0002g0010a0001c0001t0002g0016others(5): Show | 13 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+3708_-31+3709d others(4): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 120746489 | |||||
chr3:120746515
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-31+3721G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746515 | ||||||
chr3:120746675
|
C | A | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-3848C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746675 | ||||||
chr3:120746775
|
A | G | 187 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-30-3748A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746775 | ||||||
chr3:120746793
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-30-3730C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120746793 | ||||||
chr3:120747129
|
G | A | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-3394G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747129 | ||||||
chr3:120747154
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30-3369A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747154 | ||||||
chr3:120747363
|
C | T | 1 | a0002c0002t0002g0183 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-30-3160C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747363 | ||||||
chr3:120747401
|
C | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(40): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.-30-3122C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747401 | ||||||
chr3:120747422
|
A | G | 1 | a0001c0001t0001g0026 | 3 | HG02895.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-30-3101A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747422 | ||||||
chr3:120747494
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-30-3029C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747494 | ||||||
chr3:120747517
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 6 | HG02132.hp2 HG02683.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-3006C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747517 | ||||||
chr3:120747837
|
G | T | 2 | a0001c0001t0003g0024a0001c0001t0003g0141 | 4 | NA18940.hp1 NA18956.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-2686G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120747837 | ||||||
chr3:120748025
|
T | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-30-2498T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748025 | ||||||
chr3:120748027
|
T | C | 8 | a0001c0001t0001g0016a0001c0001t0002g0010a0001c0001t0002g0016others(5): Show | 13 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-2496T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748027 | ||||||
chr3:120748076
|
C | T | 40 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(37): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.-30-2447C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748076 | ||||||
chr3:120748166
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-2357A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748166 | ||||||
chr3:120748167
|
A | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-2356A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748167 | ||||||
chr3:120748170
|
G | A | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-2353G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748170 | ||||||
chr3:120748247
|
T | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0080others(2): Show | 11 | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30-2276T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748247 | ||||||
chr3:120748333
|
T | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(43): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-30-2190T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748333 | ||||||
chr3:120748413
|
G | C | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-30-2110G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748413 | ||||||
chr3:120748522
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-30-2001G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748522 | ||||||
chr3:120748563
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-30-1960A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748563 | ||||||
chr3:120748572
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-30-1951G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748572 | ||||||
chr3:120748652
|
A | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-1871A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748652 | ||||||
chr3:120748714
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-30-1809G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748714 | ||||||
chr3:120748728
|
G | A | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-1795G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748728 | ||||||
chr3:120748741
|
T | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(43): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-30-1782T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748741 | ||||||
chr3:120748805
|
C | G | 3 | a0001c0001t0002g0070a0003c0003t0005g0018a0003c0003t0005g0071 | 5 | HG01243.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30-1718C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748805 | ||||||
chr3:120748982
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-1541G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748982 | ||||||
chr3:120748985
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-1538T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120748985 | ||||||
chr3:120749130
|
T | G | 5 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188others(2): Show | 8 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-1393T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749130 | ||||||
chr3:120749203
|
A | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(183): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-30-1320A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749203 | ||||||
chr3:120749339
|
A | C | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-1184A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749339 | ||||||
chr3:120749371
|
T | G | 2 | a0001c0001t0001g0118a0006c0007t0001g0119 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-30-1152T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749371 | ||||||
chr3:120749403
|
C | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-30-1120C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749403 | ||||||
chr3:120749479
|
G | A | 1 | a0001c0001t0003g0038 | 2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-30-1044G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749479 | ||||||
chr3:120749518
|
G | T | 1 | a0001c0001t0008g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-30-1005G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749518 | ||||||
chr3:120749704
|
T | G | 1 | a0001c0006t0001g0094 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-30-819T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749704 | ||||||
chr3:120749883
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-30-640C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749883 | ||||||
chr3:120749887
|
C | T | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-30-636C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749887 | ||||||
chr3:120749931
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-30-592T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749931 | ||||||
chr3:120749953
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30-570T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749953 | ||||||
chr3:120749970
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-30-553A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749970 | ||||||
chr3:120749972
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-30-551C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120749972 | ||||||
chr3:120750031
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-30-492G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750031 | ||||||
chr3:120750106
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30-417T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750106 | ||||||
chr3:120750159
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-30-364G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750159 | ||||||
chr3:120750167
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-30-356A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750167 | ||||||
chr3:120750434
|
T | G | 3 | a0001c0001t0002g0028a0001c0001t0002g0057a0001c0001t0002g0058 | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-89T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750434 | ||||||
chr3:120750478
|
C | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-45C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750478 | ||||||
chr3:120750480
|
T | C | 1 | a0001c0001t0003g0038 | 2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-30-43T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 1/4 | chr3 | 120750480 | ||||||
chr3:120751223
|
T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(40): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.448+223T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751223 | ||||||
chr3:120751233
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.448+233G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751233 | ||||||
chr3:120751243
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+243A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751243 | ||||||
chr3:120751460
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.448+460A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751460 | ||||||
chr3:120751613
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+613A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751613 | ||||||
chr3:120751800
|
A | G | 15 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0002g0017others(12): Show | 17 | HG00558.hp1 HG01099.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.448+800A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751800 | ||||||
chr3:120751807
|
A | C | 2 | a0001c0001t0003g0015a0001c0001t0003g0140 | 5 | HG00099.hp2 HG01074.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+807A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120751807 | ||||||
chr3:120752005
|
T | C | 40 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(37): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.448+1005T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120752005 | ||||||
chr3:120752022
|
T | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(41): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.448+1022T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120752022 | ||||||
chr3:120752213
|
G | A | 1 | a0001c0001t0010g0056 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+1213G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120752213 | ||||||
chr3:120752248
|
C | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.448+1248C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120752248 | ||||||
chr3:120752582
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.448+1582G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120752582 | ||||||
chr3:120752686
|
C | T | 1 | a0002c0002t0002g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.448+1686C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120752686 | ||||||
chr3:120753012
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.448+2012T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753012 | ||||||
chr3:120753108
|
G | A | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+2108G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753108 | ||||||
chr3:120753160
|
T | C | 1 | a0002c0002t0002g0162 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.448+2160T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753160 | ||||||
chr3:120753229
|
C | T | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+2229C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753229 | ||||||
chr3:120753361
|
T | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(153): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.448+2361T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753361 | ||||||
chr3:120753363
|
G | A | 1 | a0001c0001t0003g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.448+2363G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753363 | ||||||
chr3:120753460
|
G | A | 1 | a0001c0001t0003g0038 | 2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.448+2460G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753460 | ||||||
chr3:120753681
|
G | C | 1 | a0002c0002t0002g0163 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.448+2681G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753681 | ||||||
chr3:120753758
|
A | G | 6 | a0001c0001t0001g0072a0001c0001t0002g0031a0001c0001t0002g0066others(3): Show | 7 | HG01099.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+2758A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120753758 | ||||||
chr3:120754191
|
C | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.448+3191C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754191 | ||||||
chr3:120754217
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.448+3217A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754217 | ||||||
chr3:120754273
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+3273A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754273 | ||||||
chr3:120754277
|
T | C | 1 | a0001c0001t0003g0043 | 2 | HG00642.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.448+3277T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754277 | ||||||
chr3:120754716
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0078a0001c0001t0001g0117others(1): Show | 4 | HG01109.hp1 HG02698.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+3716C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754716 | ||||||
chr3:120754723
|
C | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.448+3723C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754723 | ||||||
chr3:120754872
|
A | T | 51 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(48): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.448+3872A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754872 | ||||||
chr3:120754937
|
C | T | 6 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188others(3): Show | 9 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.448+3937C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120754937 | ||||||
chr3:120755223
|
C | T | 1 | a0006c0007t0001g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.448+4223C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755223 | ||||||
chr3:120755253
|
G | A | 1 | a0002c0002t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.448+4253G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755253 | ||||||
chr3:120755310
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.448+4310C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755310 | ||||||
chr3:120755319
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0089 | 2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.448+4319C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755319 | ||||||
chr3:120755382
|
A | C | 1 | a0002c0002t0002g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.448+4382A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755382 | ||||||
chr3:120755414
|
A | T | 1 | a0002c0002t0002g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.448+4414A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755414 | ||||||
chr3:120755493
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.448+4493A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755493 | ||||||
chr3:120755540
|
T | C | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+4540T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755540 | ||||||
chr3:120755575
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0115 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.448+4575G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755575 | ||||||
chr3:120755665
|
A | G | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.448+4665A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755665 | ||||||
chr3:120755676
|
C | T | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.448+4676C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755676 | ||||||
chr3:120755694
|
G | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0146a0006c0007t0001g0119 | 3 | HG01109.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.448+4694G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755694 | ||||||
chr3:120755706
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.448+4706T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755706 | ||||||
chr3:120755813
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.448+4813G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755813 | ||||||
chr3:120755990
|
A | C | 1 | a0001c0001t0002g0069 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.448+4990A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120755990 | ||||||
chr3:120756027
|
G | A | 1 | a0001c0001t0003g0129 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.448+5027G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756027 | ||||||
chr3:120756080
|
C | T | 1 | a0001c0001t0003g0048 | 2 | HG00140.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.448+5080C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756080 | ||||||
chr3:120756091
|
G | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.448+5091G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756091 | ||||||
chr3:120756101
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.448+5101T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756101 | ||||||
chr3:120756142
|
G | C | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+5142G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756142 | ||||||
chr3:120756236
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.448+5236G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756236 | ||||||
chr3:120756256
|
G | A | 1 | a0001c0001t0004g0055 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.448+5256G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756256 | ||||||
chr3:120756342
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.448+5342A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756342 | ||||||
chr3:120756523
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+5523A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756523 | ||||||
chr3:120756706
|
G | A | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.448+5706G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756706 | ||||||
chr3:120756787
|
G | A | 1 | a0001c0001t0004g0054 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.448+5787G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756787 | ||||||
chr3:120756799
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.448+5799G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756799 | ||||||
chr3:120756875
|
G | A | 3 | a0001c0001t0003g0012a0001c0001t0003g0130a0001c0001t0003g0131 | 7 | HG01123.hp2 HG01928.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+5875G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756875 | ||||||
chr3:120756879
|
T | C | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+5879T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756879 | ||||||
chr3:120756880
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.448+5880C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756880 | ||||||
chr3:120756881
|
G | A | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+5881G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756881 | ||||||
chr3:120756917
|
C | T | 1 | a0001c0001t0001g0052 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.448+5917C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120756917 | ||||||
chr3:120757059
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.448+6059C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757059 | ||||||
chr3:120757233
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.448+6233G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757233 | ||||||
chr3:120757465
|
TCTG | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0080others(2): Show | 11 | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.448+6466_448+6468d others(5): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757465 | ||||||
chr3:120757484
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.448+6484A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757484 | ||||||
chr3:120757707
|
C | T | 2 | a0002c0002t0002g0186a0002c0002t0002g0187 | 2 | NA18999.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.448+6707C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757707 | ||||||
chr3:120757780
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.448+6780T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757780 | ||||||
chr3:120757809
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.448+6809G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757809 | ||||||
chr3:120757863
|
A | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+6863A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120757863 | ||||||
chr3:120758037
|
G | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(13): Show | 22 | HG00639.hp1 HG00735.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.448+7037G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758037 | ||||||
chr3:120758079
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0115 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.448+7079G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758079 | ||||||
chr3:120758118
|
C | T | 1 | a0002c0002t0002g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.448+7118C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758118 | ||||||
chr3:120758138
|
A | C | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+7138A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758138 | ||||||
chr3:120758142
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0122a0001c0001t0001g0123 | 4 | HG01358.hp1 HG01433.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+7142C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758142 | ||||||
chr3:120758250
|
C | T | 2 | a0002c0002t0002g0178a0002c0002t0002g0179 | 2 | NA19057.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.448+7250C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758250 | ||||||
chr3:120758311
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.448+7311C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758311 | ||||||
chr3:120758502
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.448+7502A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758502 | ||||||
chr3:120758585
|
C | CT | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.448+7585_448+7586i others(3): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758585 | ||||||
chr3:120758633
|
C | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.448+7633C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758633 | ||||||
chr3:120758882
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.448+7882C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758882 | ||||||
chr3:120758889
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.448+7889A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758889 | ||||||
chr3:120758892
|
T | A | 12 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0044others(9): Show | 22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.448+7892T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120758892 | ||||||
chr3:120759063
|
C | T | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.448+8063C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759063 | ||||||
chr3:120759154
|
T | C | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+8154T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759154 | ||||||
chr3:120759205
|
G | A | 41 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.448+8205G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759205 | ||||||
chr3:120759224
|
G | A | 5 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188others(2): Show | 8 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+8224G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759224 | ||||||
chr3:120759226
|
A | G | 2 | a0001c0001t0004g0054a0001c0001t0004g0188 | 3 | HG02145.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.448+8226A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759226 | ||||||
chr3:120759331
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0002g0016a0001c0001t0002g0063 | 4 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+8331G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759331 | ||||||
chr3:120759772
|
G | A | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+8772G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759772 | ||||||
chr3:120759842
|
C | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+8842C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120759842 | ||||||
chr3:120760108
|
C | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+9108C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760108 | ||||||
chr3:120760171
|
G | A | 3 | a0001c0001t0002g0028a0001c0001t0002g0057a0001c0001t0002g0058 | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+9171G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760171 | ||||||
chr3:120760194
|
A | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0152others(4): Show | 11 | HG00735.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.448+9194A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760194 | ||||||
chr3:120760280
|
T | G | 3 | a0002c0002t0002g0053a0002c0002t0002g0164a0002c0002t0002g0165 | 4 | HG01074.hp1 HG01358.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+9280T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760280 | ||||||
chr3:120760316
|
A | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+9316A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760316 | ||||||
chr3:120760360
|
C | G | 15 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0002g0017others(12): Show | 17 | HG00558.hp1 HG01099.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.448+9360C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760360 | ||||||
chr3:120760657
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(200): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.448+9657A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760657 | ||||||
chr3:120760739
|
A | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+9739A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760739 | ||||||
chr3:120760775
|
C | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(8): Show | 17 | HG00735.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.448+9775C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760775 | ||||||
chr3:120760850
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0093a0001c0001t0001g0110others(1): Show | 6 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+9850C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760850 | ||||||
chr3:120760918
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.449-9810A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120760918 | ||||||
chr3:120761287
|
G | A | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-9441G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761287 | ||||||
chr3:120761304
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.449-9424C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761304 | ||||||
chr3:120761559
|
G | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-9169G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761559 | ||||||
chr3:120761633
|
T | C | 1 | a0002c0002t0002g0166 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.449-9095T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761633 | ||||||
chr3:120761651
|
T | G | 2 | a0001c0001t0001g0118a0006c0007t0001g0119 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.449-9077T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761651 | ||||||
chr3:120761759
|
A | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-8969A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761759 | ||||||
chr3:120761786
|
A | AT | 16 | a0001c0001t0001g0076a0001c0001t0001g0121a0001c0001t0001g0143others(13): Show | 17 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.449-8920dupT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120761786 | |||||
chr3:120761786
|
AT | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0034others(56): Show | 130 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.449-8920delT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120761786 | |||||
chr3:120761786
|
ATT | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0002g0028others(7): Show | 12 | HG01099.hp2 HG01975.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-8921_449-8920d others(4): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120761786 | |||||
chr3:120761786
|
ATTTTTTT others(7): Show |
A | 23 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(20): Show | 37 | HG00323.hp2 HG00621.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.449-8933_449-8920d others(16): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120761786 | |||||
chr3:120761898
|
C | A | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.449-8830C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761898 | ||||||
chr3:120761964
|
G | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-8764G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761964 | ||||||
chr3:120761983
|
G | A | 1 | a0001c0001t0010g0056 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.449-8745G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120761983 | ||||||
chr3:120762011
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.449-8717C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762011 | ||||||
chr3:120762079
|
C | A | 14 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0009others(11): Show | 38 | HG00423.hp2 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.449-8649C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762079 | ||||||
chr3:120762086
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.449-8642G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762086 | ||||||
chr3:120762169
|
T | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.449-8559T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762169 | ||||||
chr3:120762520
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0106 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.449-8208A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762520 | ||||||
chr3:120762559
|
A | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0036others(12): Show | 26 | HG00621.hp1 HG01243.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.449-8169A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762559 | ||||||
chr3:120762658
|
C | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-8070C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762658 | ||||||
chr3:120762767
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.449-7961A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762767 | ||||||
chr3:120762777
|
G | A | 1 | a0001c0001t0003g0140 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.449-7951G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762777 | ||||||
chr3:120762875
|
C | T | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-7853C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762875 | ||||||
chr3:120762931
|
A | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-7797A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120762931 | ||||||
chr3:120763028
|
A | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-7700A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120763028 | ||||||
chr3:120763142
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.449-7586G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120763142 | ||||||
chr3:120763282
|
C | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-7446C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120763282 | ||||||
chr3:120763485
|
G | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.449-7243G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120763485 | ||||||
chr3:120763676
|
A | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(38): Show | 77 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.449-7052A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120763676 | ||||||
chr3:120763719
|
C | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(43): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.449-7009C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120763719 | ||||||
chr3:120764089
|
C | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-6639C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764089 | ||||||
chr3:120764129
|
G | C | 1 | a0002c0002t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.449-6599G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764129 | ||||||
chr3:120764144
|
C | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0048 | 7 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-6584C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764144 | ||||||
chr3:120764198
|
T | A | 1 | a0002c0002t0002g0169 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.449-6530T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764198 | ||||||
chr3:120764252
|
C | A | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-6476C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764252 | ||||||
chr3:120764376
|
G | A | 2 | a0001c0001t0001g0118a0006c0007t0001g0119 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.449-6352G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764376 | ||||||
chr3:120764390
|
T | C | 51 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(48): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.449-6338T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764390 | ||||||
chr3:120764420
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0120others(5): Show | 11 | HG01358.hp1 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.449-6308A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764420 | ||||||
chr3:120764714
|
G | A | 6 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188others(3): Show | 9 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-6014G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764714 | ||||||
chr3:120764978
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.449-5750G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120764978 | ||||||
chr3:120764991
|
G | GT | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.449-5726dupT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120764991 | |||||
chr3:120764991
|
GT | G | 8 | a0001c0001t0001g0016a0001c0001t0002g0010a0001c0001t0002g0016others(5): Show | 13 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.449-5726delT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120764991 | |||||
chr3:120765125
|
C | T | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-5603C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120765125 | ||||||
chr3:120765298
|
AT | A | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.449-5423delT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120765298 | |||||
chr3:120765394
|
A | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-5334A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120765394 | ||||||
chr3:120765499
|
G | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0142others(3): Show | 8 | HG02132.hp2 HG02683.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-5229G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120765499 | ||||||
chr3:120765518
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.449-5210G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120765518 | ||||||
chr3:120765621
|
T | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-5107T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120765621 | ||||||
chr3:120765652
|
T | C | 2 | a0001c0001t0003g0129a0001c0001t0003g0134 | 2 | NA18964.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.449-5076T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120765652 | ||||||
chr3:120766059
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.449-4669A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766059 | ||||||
chr3:120766260
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0004g0188 | 3 | HG02145.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.449-4468C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766260 | ||||||
chr3:120766318
|
C | T | 1 | a0001c0001t0008g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.449-4410C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766318 | ||||||
chr3:120766351
|
G | T | 2 | a0002c0002t0002g0163a0002c0002t0002g0175 | 2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.449-4377G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766351 | ||||||
chr3:120766461
|
C | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-4267C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766461 | ||||||
chr3:120766469
|
T | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.449-4259T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766469 | ||||||
chr3:120766525
|
T | C | 1 | a0001c0001t0003g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.449-4203T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766525 | ||||||
chr3:120766674
|
C | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.449-4054C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766674 | ||||||
chr3:120766785
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0123 | 3 | HG01358.hp1 HG01433.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.449-3943G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766785 | ||||||
chr3:120766823
|
G | A | 1 | a0001c0001t0003g0022 | 3 | NA18974.hp1 NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.449-3905G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766823 | ||||||
chr3:120766862
|
G | A | 59 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0072others(56): Show | 116 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.449-3866G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120766862 | ||||||
chr3:120767281
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.449-3447G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120767281 | ||||||
chr3:120767396
|
A | G | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.449-3332A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120767396 | ||||||
chr3:120767536
|
C | T | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.449-3192C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120767536 | ||||||
chr3:120767720
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0091 | 3 | HG00280.hp2 HG00735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.449-3008T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120767720 | ||||||
chr3:120767741
|
C | T | 1 | a0001c0001t0003g0023 | 3 | NA18955.hp1 NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.449-2987C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120767741 | ||||||
chr3:120767770
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0105 | 4 | HG00621.hp1 NA18959.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-2958C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120767770 | ||||||
chr3:120767935
|
TTC | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(38): Show | 77 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.449-2789_449-2788d others(4): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120767935 | |||||
chr3:120768103
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(40): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.449-2625A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768103 | ||||||
chr3:120768116
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0069 | 2 | HG01099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.449-2612G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768116 | ||||||
chr3:120768209
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.449-2519A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768209 | ||||||
chr3:120768281
|
T | G | 1 | a0001c0001t0002g0039 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.449-2447T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768281 | ||||||
chr3:120768326
|
G | A | 1 | a0001c0001t0017g0189 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.449-2402G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768326 | ||||||
chr3:120768389
|
G | A | 1 | a0001c0001t0017g0189 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.449-2339G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768389 | ||||||
chr3:120768493
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.449-2235A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768493 | ||||||
chr3:120768495
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.449-2233A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768495 | ||||||
chr3:120768759
|
A | C | 1 | a0001c0001t0001g0050 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.449-1969A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120768759 | ||||||
chr3:120769091
|
A | G | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.449-1637A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769091 | ||||||
chr3:120769093
|
T | G | 1 | a0001c0001t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.449-1635T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769093 | ||||||
chr3:120769196
|
T | TA | 7 | a0001c0001t0001g0110a0001c0001t0008g0051a0001c0001t0009g0051others(4): Show | 8 | HG02055.hp1 HG02738.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-1517dupA | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120769196 | |||||
chr3:120769196
|
T | TAAA | 4 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188others(1): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-1519_449-1517d others(5): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 120769196 | |||||
chr3:120769241
|
A | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(40): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.449-1487A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769241 | ||||||
chr3:120769322
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-1406A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769322 | ||||||
chr3:120769520
|
A | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1208A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769520 | ||||||
chr3:120769702
|
A | G | 2 | a0001c0001t0001g0118a0006c0007t0001g0119 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.449-1026A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769702 | ||||||
chr3:120769810
|
C | T | 1 | a0001c0001t0003g0038 | 2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.449-918C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769810 | ||||||
chr3:120769824
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.449-904T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769824 | ||||||
chr3:120769850
|
A | G | 2 | a0001c0001t0003g0022a0001c0001t0003g0138 | 4 | NA18974.hp1 NA18980.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-878A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769850 | ||||||
chr3:120769853
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.449-875T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120769853 | ||||||
chr3:120770092
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.449-636C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120770092 | ||||||
chr3:120770272
|
T | A | 2 | a0001c0001t0004g0054a0001c0001t0004g0188 | 3 | HG02145.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.449-456T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120770272 | ||||||
chr3:120770547
|
G | A | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.449-181G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120770547 | ||||||
chr3:120770680
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0003g0014a0001c0001t0003g0137others(1): Show | 6 | HG00609.hp1 NA18962.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-48A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120770680 | ||||||
chr3:120770684
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0002g0010a0001c0001t0002g0016others(5): Show | 13 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.449-44G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 2/4 | chr3 | 120770684 | ||||||
chr3:120770980
|
G | GT | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.650+55dupT | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 120770980 | |||||
chr3:120771079
|
G | T | 51 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(48): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.650+150G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771079 | ||||||
chr3:120771105
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0152others(4): Show | 11 | HG00735.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.650+176C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771105 | ||||||
chr3:120771166
|
G | A | 1 | a0002c0002t0002g0165 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.650+237G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771166 | ||||||
chr3:120771337
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.650+408C>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771337 | ||||||
chr3:120771606
|
T | C | 1 | a0001c0001t0009g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.650+677T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771606 | ||||||
chr3:120771637
|
A | C | 1 | a0001c0001t0008g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.650+708A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771637 | ||||||
chr3:120771665
|
T | C | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.650+736T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120771665 | ||||||
chr3:120772041
|
C | T | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.650+1112C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772041 | ||||||
chr3:120772069
|
G | A | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.650+1140G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772069 | ||||||
chr3:120772092
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.650+1163T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772092 | ||||||
chr3:120772109
|
C | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.650+1180C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772109 | ||||||
chr3:120772146
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.650+1217C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772146 | ||||||
chr3:120772147
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.650+1218G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772147 | ||||||
chr3:120772175
|
T | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0142others(3): Show | 8 | HG02132.hp2 HG02683.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.650+1246T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772175 | ||||||
chr3:120772184
|
G | T | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.650+1255G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772184 | ||||||
chr3:120772210
|
T | G | 7 | a0001c0001t0003g0046a0001c0001t0003g0074a0001c0001t0003g0127others(4): Show | 8 | HG00099.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.650+1281T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772210 | ||||||
chr3:120772239
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(169): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.650+1310G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772239 | ||||||
chr3:120772286
|
A | G | 3 | a0002c0002t0002g0007a0002c0002t0002g0167a0002c0002t0002g0177 | 10 | HG00423.hp2 NA18952.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.650+1357A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772286 | ||||||
chr3:120772313
|
T | TA | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.650+1385dupA | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 120772313 | |||||
chr3:120772540
|
A | G | 33 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0007others(30): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.650+1611A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772540 | ||||||
chr3:120772659
|
G | A | 34 | a0001c0001t0001g0095a0002c0002t0002g0001a0002c0002t0002g0005others(31): Show | 83 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.650+1730G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772659 | ||||||
chr3:120772897
|
A | G | 1 | a0002c0002t0002g0174 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.650+1968A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772897 | ||||||
chr3:120772946
|
A | G | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(8): Show | 17 | HG00735.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.650+2017A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772946 | ||||||
chr3:120772949
|
T | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(8): Show | 17 | HG00735.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.650+2020T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120772949 | ||||||
chr3:120773062
|
G | C | 1 | a0005c0005t0001g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.650+2133G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773062 | ||||||
chr3:120773153
|
AAAAC | A | 40 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(37): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.650+2225_650+2228d others(6): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773153 | ||||||
chr3:120773220
|
C | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.650+2291C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773220 | ||||||
chr3:120773456
|
C | A | 1 | a0001c0001t0003g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.650+2527C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773456 | ||||||
chr3:120773557
|
T | C | 1 | a0001c0001t0003g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.650+2628T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773557 | ||||||
chr3:120773581
|
A | G | 45 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(42): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.650+2652A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773581 | ||||||
chr3:120773732
|
A | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(127): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.651-2691A>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773732 | ||||||
chr3:120773922
|
A | G | 1 | a0001c0001t0003g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.651-2501A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120773922 | ||||||
chr3:120774069
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.651-2354G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774069 | ||||||
chr3:120774077
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.651-2346C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774077 | ||||||
chr3:120774175
|
T | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.651-2248T>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774175 | ||||||
chr3:120774403
|
C | T | 15 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0002g0017others(12): Show | 17 | HG00558.hp1 HG01099.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.651-2020C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774403 | ||||||
chr3:120774545
|
A | G | 11 | a0001c0001t0001g0016a0001c0001t0002g0010a0001c0001t0002g0016others(8): Show | 17 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.651-1878A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774545 | ||||||
chr3:120774551
|
A | T | 1 | a0001c0001t0002g0031 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.651-1872A>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774551 | ||||||
chr3:120774606
|
A | G | 1 | a0002c0002t0002g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.651-1817A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774606 | ||||||
chr3:120774633
|
CA | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(110): Show | 214 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.651-1774delA | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 120774633 | |||||
chr3:120774633
|
CAA | C | 51 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0049others(48): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.651-1775_651-1774d others(4): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 120774633 | |||||
chr3:120774633
|
CAAA | C | 6 | a0001c0001t0003g0038a0001c0001t0003g0046a0001c0001t0003g0127others(3): Show | 9 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.651-1776_651-1774d others(5): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 120774633 | |||||
chr3:120774786
|
C | T | 1 | a0001c0001t0003g0141 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.651-1637C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774786 | ||||||
chr3:120774803
|
T | C | 1 | a0002c0002t0002g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.651-1620T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774803 | ||||||
chr3:120774803
|
TG | T | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.651-1617delG | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 120774803 | |||||
chr3:120774866
|
C | T | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.651-1557C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120774866 | ||||||
chr3:120775085
|
C | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0188 | 5 | HG01891.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.651-1338C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120775085 | ||||||
chr3:120775248
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.651-1175G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120775248 | ||||||
chr3:120775442
|
C | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(94): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.651-981C>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120775442 | ||||||
chr3:120775556
|
G | C | 1 | a0002c0002t0002g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.651-867G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120775556 | ||||||
chr3:120775870
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.651-553G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120775870 | ||||||
chr3:120776262
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.651-161G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 3/4 | chr3 | 120776262 | ||||||
chr3:120776821
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.892+157A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120776821 | ||||||
chr3:120777125
|
G | C | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.892+461G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777125 | ||||||
chr3:120777151
|
C | T | 1 | a0001c0001t0004g0055 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.892+487C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777151 | ||||||
chr3:120777195
|
G | C | 51 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0013others(48): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.892+531G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777195 | ||||||
chr3:120777262
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.892+598G>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777262 | ||||||
chr3:120777526
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0108 | 2 | HG02015.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.892+862C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777526 | ||||||
chr3:120777702
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.892+1038C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777702 | ||||||
chr3:120777710
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.892+1046C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777710 | ||||||
chr3:120777868
|
C | T | 1 | a0001c0001t0004g0055 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.892+1204C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777868 | ||||||
chr3:120777913
|
G | A | 1 | a0001c0001t0017g0189 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.892+1249G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120777913 | ||||||
chr3:120778032
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.892+1368T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778032 | ||||||
chr3:120778055
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.892+1391A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778055 | ||||||
chr3:120778405
|
G | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(13): Show | 22 | HG00639.hp1 HG00735.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.892+1741G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778405 | ||||||
chr3:120778446
|
A | G | 1 | a0001c0001t0012g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.892+1782A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778446 | ||||||
chr3:120778473
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.892+1809A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778473 | ||||||
chr3:120778737
|
G | A | 2 | a0002c0002t0002g0171a0002c0002t0002g0176 | 2 | NA18949.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.892+2073G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778737 | ||||||
chr3:120778943
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.893-2100T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778943 | ||||||
chr3:120778988
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(43): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.893-2055G>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778988 | ||||||
chr3:120778998
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.893-2045C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120778998 | ||||||
chr3:120779278
|
T | TA | 2 | a0001c0001t0010g0056a0001c0001t0017g0189 | 3 | HG02055.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.893-1764dupA | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 120779278 | |||||
chr3:120779422
|
G | T | 1 | a0002c0002t0002g0162 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.893-1621G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120779422 | ||||||
chr3:120779669
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(9): Show | 18 | HG00735.hp1 HG02257.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.893-1374C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120779669 | ||||||
chr3:120779983
|
C | T | 1 | a0002c0002t0002g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.893-1060C>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120779983 | ||||||
chr3:120780265
|
A | G | 1 | a0006c0007t0001g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.893-778A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120780265 | ||||||
chr3:120780491
|
A | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0071 | 4 | HG01243.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.893-552A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120780491 | ||||||
chr3:120780613
|
G | GAGTGAGC others(3): Show |
4 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0145others(1): Show | 6 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.893-424_893-423ins others(10): Show |
GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 120780613 | |||||
chr3:120780834
|
T | A | 1 | a0002c0002t0002g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.893-209T>A | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120780834 | ||||||
chr3:120780848
|
T | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0082 | 3 | HG01106.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.893-195T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120780848 | ||||||
chr3:120780878
|
G | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(40): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.893-165G>T | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120780878 | ||||||
chr3:120780980
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.893-63A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120780980 | ||||||
chr3:120781014
|
A | G | 1 | a0001c0001t0001g0037 | 2 | NA18971.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.893-29A>G | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120781014 | ||||||
chr3:120781024
|
T | C | 1 | a0001c0001t0003g0044 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.893-19T>C | GTF2E1 | ENSG00000153767.10 | transcript | ENST00000283875.6 | protein_coding | 4/4 | chr3 | 120781024 |