geneid | 57117 |
---|---|
ensemblid | ENSG00000138785.16 |
hgncid | 25067 |
symbol | INTS12 |
name | integrator complex subunit 12 |
refseq_nuc | NM_020395.4 |
refseq_prot | NP_065128.2 |
ensembl_nuc | ENST00000340139.10 |
ensembl_prot | ENSP00000340737.5 |
mane_status | MANE Select |
chr | chr4 |
start | 105682627 |
end | 105708689 |
strand | - |
ver | v1.2 |
region | chr4:105682627-105708689 |
region5000 | chr4:105677627-105713689 |
regionname0 | INTS12_chr4_105682627_105708689 |
regionname5000 | INTS12_chr4_105677627_105713689 |
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 | 462 | 309 | 90 | 56 | 131 | 14 | 16 | 99 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0002 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0003 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0004 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
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 | 1389 | 289 | 83 | 46 | 130 | 13 | 15 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0002 | 0/0 | 1389 | 10 | 0 | 8 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0003 | 0/0 | 1389 | 5 | 3 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0004 | 0/0 | 1389 | 3 | 3 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0005 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0006 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0007 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0008 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
c0009 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
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 | 330 | 300 | 90 | 56 | 123 | 14 | 15 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
t0002 | 0/0 | 330 | 5 | 0 | 0 | 5 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
t0003 | 0/0 | 330 | 4 | 0 | 0 | 3 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
t0004 | 0/0 | 330 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
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 | 1/0 | 29 | 1 | 6 | 12 | 5 | 4 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0002 | 0/0 | 18 | 4 | 4 | 9 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0005 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0011 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0012 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0015 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
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 | 1389 | 289 | 83 | 46 | 130 | 13 | 15 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0002 | 0/0 | 1389 | 10 | 0 | 8 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0003 | 0/0 | 1389 | 5 | 3 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0004 | 0/0 | 1389 | 3 | 3 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0005 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0009 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0002c0008 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0003c0007 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0004c0006 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1718 | 277 | 83 | 46 | 119 | 13 | 14 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0001t0002 | 0/0 | 1718 | 5 | 0 | 0 | 5 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0001t0003 | 0/0 | 1718 | 4 | 0 | 0 | 3 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0001t0004 | 0/0 | 1718 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0002t0001 | 0/0 | 1718 | 10 | 0 | 8 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0003t0001 | 0/0 | 1718 | 5 | 3 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0004t0001 | 0/0 | 1718 | 3 | 3 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0005t0001 | 0/0 | 1718 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0001c0009t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0002c0008t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0003c0007t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
a0004c0006t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | copy fasta | chr4 | 105677627 | 105713689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 29 | 1 | 6 | 12 | 5 | 4 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0002 | 0/0 | 18 | 4 | 4 | 9 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0005 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0015 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0002t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0003t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0001c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0002c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0003c0007t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
a0004c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02129 | hp2 | a0001 | c0009 | t0001 | g0117 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0147 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0073 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18954 | hp2 | a0002 | c0008 | t0001 | g0150 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19060 | hp2 | a0003 | c0007 | t0001 | g0115 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19086 | hp2 | a0004 | c0006 | t0001 | g0089 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0183 | REF | REF | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105682822
|
C | T | 1 | a0004 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.1300G>A | p.Gly434Ser | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1523/1718 | 1300/1389 | 434/462 | chr4 | 105682822 | ||
chr4:105683151
|
G | A | 1 | a0003 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.971C>T | p.Ser324Leu | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1194/1718 | 971/1389 | 324/462 | chr4 | 105683151 | ||
chr4:105683278
|
C | A | 1 | a0002 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.844G>T | p.Val282Phe | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1067/1718 | 844/1389 | 282/462 | chr4 | 105683278 | ||
chr4:105700012
|
C | T | 1 | a0001 | 5 | NA18942.hp1 NA18968.hp1 NA19005.hp1 others(2): Show |
splice_region_variant | LOW | c.-7G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/8 | chr4 | 105700012 | ||||||
chr4:105700013
|
G | A | 1 | a0001 | 3 | NA18952.hp2 NA18953.hp2 NA18954.hp1 |
splice_region_variant | LOW | c.-8C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/8 | chr4 | 105700013 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105682823
|
T | C | 1 | a0004c0006 | 1 | NA19086.hp2 | synonymous_variant | LOW | c.1299A>G | p.Lys433Lys | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1522/1718 | 1299/1389 | 433/462 | chr4 | 105682823 | ||
chr4:105682913
|
C | T | 1 | a0001c0005 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1209G>A | p.Gly403Gly | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1432/1718 | 1209/1389 | 403/462 | chr4 | 105682913 | ||
chr4:105683033
|
A | G | 1 | a0001c0002 | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
synonymous_variant | LOW | c.1089T>C | p.Pro363Pro | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1312/1718 | 1089/1389 | 363/462 | chr4 | 105683033 | ||
chr4:105683207
|
A | G | 2 | a0001c0002a0001c0003 | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
synonymous_variant | LOW | c.915T>C | p.Pro305Pro | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1138/1718 | 915/1389 | 305/462 | chr4 | 105683207 | ||
chr4:105692054
|
G | C | 1 | a0001c0004 | 3 | HG02630.hp2 HG03516.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.579C>G | p.Pro193Pro | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/8 | 802/1718 | 579/1389 | 193/462 | chr4 | 105692054 | ||
chr4:105695534
|
T | C | 1 | a0001c0009 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.291A>G | p.Glu97Glu | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/8 | 514/1718 | 291/1389 | 97/462 | chr4 | 105695534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105682704
|
A | G | 1 | a0001c0001t0003 | 4 | HG00673.hp1 HG02056.hp1 HG02074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*29T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 29 | chr4 | 105682704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105683428
|
T | C | 1 | a0001c0005t0001g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.805-111A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683428 | ||||||
chr4:105683525
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.805-208C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683525 | ||||||
chr4:105683629
|
G | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-312C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683629 | ||||||
chr4:105683672
|
A | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016others(19): Show | 35 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.805-355T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683672 | ||||||
chr4:105683690
|
C | A | 1 | a0001c0001t0001g0145 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.805-373G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683690 | ||||||
chr4:105683733
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.805-416A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683733 | ||||||
chr4:105683835
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.805-518T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683835 | ||||||
chr4:105683840
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0130a0001c0001t0001g0131 | 4 | NA18971.hp1 NA19003.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-523A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683840 | ||||||
chr4:105683892
|
G | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0004t0001g0071others(2): Show | 5 | HG01070.hp1 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-575C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683892 | ||||||
chr4:105684085
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.805-768C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684085 | ||||||
chr4:105684136
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.805-819G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684136 | ||||||
chr4:105684302
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0075others(1): Show | 6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-985A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684302 | ||||||
chr4:105684563
|
A | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-1246T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684563 | ||||||
chr4:105684795
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.805-1478A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684795 | ||||||
chr4:105684859
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0187a0001c0001t0001g0193 | 4 | NA18990.hp1 NA18994.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1542G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684859 | ||||||
chr4:105685013
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.804+1679T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685013 | ||||||
chr4:105685154
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0075others(1): Show | 6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+1538A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685154 | ||||||
chr4:105685392
|
C | T | 1 | a0001c0005t0001g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.804+1300G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685392 | ||||||
chr4:105685412
|
C | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.804+1280G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685412 | ||||||
chr4:105685451
|
A | G | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.804+1241T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685451 | ||||||
chr4:105685660
|
AT | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+1031delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685660 | ||||||
chr4:105685694
|
T | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0165 | 3 | HG02074.hp2 NA18974.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.804+998A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685694 | ||||||
chr4:105685816
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.804+876A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685816 | ||||||
chr4:105686084
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(92): Show | 142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.804+608A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686084 | ||||||
chr4:105686157
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0132a0001c0001t0001g0152 | 3 | HG00642.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.804+535C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686157 | ||||||
chr4:105686336
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.804+356C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686336 | ||||||
chr4:105686389
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.804+303A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686389 | ||||||
chr4:105686650
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.804+42T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686650 | ||||||
chr4:105687054
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.658-216C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105687054 | ||||||
chr4:105687821
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0076 | 4 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-983G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105687821 | ||||||
chr4:105687908
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0157 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.658-1070C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105687908 | ||||||
chr4:105688247
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0119others(1): Show | 8 | HG00438.hp2 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.658-1409C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105688247 | ||||||
chr4:105689193
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.658-2355A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689193 | ||||||
chr4:105689211
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0129a0001c0001t0001g0162 | 4 | HG00408.hp2 NA18747.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-2373C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689211 | ||||||
chr4:105689241
|
C | T | 1 | a0001c0001t0001g0039 | 2 | NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.658-2403G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689241 | ||||||
chr4:105689274
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.658-2436C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689274 | ||||||
chr4:105689280
|
T | A | 2 | a0001c0001t0001g0030a0003c0007t0001g0115 | 3 | HG00544.hp2 NA18979.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.658-2442A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689280 | ||||||
chr4:105689499
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0075others(1): Show | 6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+2477G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689499 | ||||||
chr4:105689502
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.657+2474T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689502 | ||||||
chr4:105689642
|
C | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0098 | 4 | HG01175.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+2334G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689642 | ||||||
chr4:105689764
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.657+2212C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689764 | ||||||
chr4:105689774
|
C | T | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.657+2202G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689774 | ||||||
chr4:105689782
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.657+2194A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689782 | ||||||
chr4:105689857
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.657+2119C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689857 | ||||||
chr4:105690052
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.657+1924T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690052 | ||||||
chr4:105690103
|
A | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(93): Show | 143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.657+1873T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690103 | ||||||
chr4:105690380
|
A | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+1596T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690380 | ||||||
chr4:105690458
|
CAT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 48 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.657+1516_657+1517d others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690458 | ||||||
chr4:105690486
|
G | A | 2 | a0001c0003t0001g0018a0001c0003t0001g0065 | 3 | HG00735.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.657+1490C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690486 | ||||||
chr4:105690648
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.657+1328T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690648 | ||||||
chr4:105690950
|
G | T | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+1026C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690950 | ||||||
chr4:105691119
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.657+857G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691119 | ||||||
chr4:105691461
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657+515A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691461 | ||||||
chr4:105691576
|
G | A | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0127others(4): Show | 9 | HG00544.hp1 NA18939.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.657+400C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691576 | ||||||
chr4:105691692
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0076 | 4 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+284A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691692 | ||||||
chr4:105691696
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0155a0001c0001t0001g0161others(1): Show | 5 | HG01433.hp2 NA18990.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+280A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691696 | ||||||
chr4:105691837
|
A | T | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+139T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691837 | ||||||
chr4:105691839
|
A | G | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0069others(11): Show | 16 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+137T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691839 | ||||||
chr4:105691929
|
A | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0157 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.657+47T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691929 | ||||||
chr4:105692342
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498-207C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692342 | ||||||
chr4:105692479
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0075others(1): Show | 6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-344C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692479 | ||||||
chr4:105692483
|
C | CA | 20 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0075others(17): Show | 21 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.498-349dupT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692483 | ||||||
chr4:105692483
|
CA | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0134others(3): Show | 6 | HG01167.hp1 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-349delT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692483 | ||||||
chr4:105692596
|
T | C | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-461A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692596 | ||||||
chr4:105692664
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(51): Show | 84 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.498-529T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692664 | ||||||
chr4:105693127
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.497+172A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105693127 | ||||||
chr4:105693180
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.497+119T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105693180 | ||||||
chr4:105693539
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.310-53A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693539 | ||||||
chr4:105693570
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0075others(1): Show | 6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-84A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693570 | ||||||
chr4:105693598
|
T | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(8): Show | 22 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.310-112A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693598 | ||||||
chr4:105693620
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.310-134C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693620 | ||||||
chr4:105693649
|
T | C | 20 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 24 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.310-163A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693649 | ||||||
chr4:105693869
|
CA | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.310-384delT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693869 | ||||||
chr4:105693874
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.310-388A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693874 | ||||||
chr4:105694446
|
C | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.310-960G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694446 | ||||||
chr4:105694480
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.310-994G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694480 | ||||||
chr4:105694581
|
T | C | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+935A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694581 | ||||||
chr4:105694865
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.309+651G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694865 | ||||||
chr4:105694885
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.309+631A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694885 | ||||||
chr4:105694987
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.309+529G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694987 | ||||||
chr4:105695034
|
C | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+482G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695034 | ||||||
chr4:105695041
|
C | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+475G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695041 | ||||||
chr4:105695043
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.309+473G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695043 | ||||||
chr4:105695057
|
C | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+459G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695057 | ||||||
chr4:105695210
|
C | T | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.309+306G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695210 | ||||||
chr4:105695935
|
C | A | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-267G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105695935 | ||||||
chr4:105695979
|
G | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.157-311C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105695979 | ||||||
chr4:105695996
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.157-328C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105695996 | ||||||
chr4:105696014
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 51 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-346C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696014 | ||||||
chr4:105696044
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.157-376C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696044 | ||||||
chr4:105696093
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0112a0001c0001t0001g0118 | 5 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-425G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696093 | ||||||
chr4:105696133
|
G | A | 2 | a0001c0002t0001g0009a0001c0002t0001g0020 | 6 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-465C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696133 | ||||||
chr4:105696204
|
G | A | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-536C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696204 | ||||||
chr4:105696394
|
T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0124others(1): Show | 7 | NA18747.hp2 NA18952.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-726A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696394 | ||||||
chr4:105697062
|
A | G | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-1394T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697062 | ||||||
chr4:105697205
|
T | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.157-1537A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697205 | ||||||
chr4:105697344
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157-1676C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697344 | ||||||
chr4:105697382
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-1714A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697382 | ||||||
chr4:105697429
|
G | GA | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-1762dupT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697429 | ||||||
chr4:105697459
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.157-1791G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697459 | ||||||
chr4:105697597
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.157-1929G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697597 | ||||||
chr4:105697705
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157-2037C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697705 | ||||||
chr4:105697791
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0069others(11): Show | 16 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+2059A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697791 | ||||||
chr4:105697793
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0004t0001g0071others(2): Show | 5 | HG01070.hp1 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+2057A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697793 | ||||||
chr4:105697912
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 51 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+1938A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697912 | ||||||
chr4:105697914
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.156+1936C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697914 | ||||||
chr4:105697983
|
G | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+1867C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697983 | ||||||
chr4:105698072
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.156+1778T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698072 | ||||||
chr4:105698156
|
C | T | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.156+1694G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698156 | ||||||
chr4:105698187
|
T | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.156+1663A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698187 | ||||||
chr4:105698220
|
T | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(9): Show | 23 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.156+1630A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698220 | ||||||
chr4:105698554
|
A | AT | 45 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 69 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.156+1295dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698554 | ||||||
chr4:105698571
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.156+1279T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698571 | ||||||
chr4:105698852
|
G | A | 2 | a0001c0003t0001g0018a0001c0003t0001g0065 | 3 | HG00735.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.156+998C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698852 | ||||||
chr4:105699040
|
A | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0128a0001c0001t0001g0135others(2): Show | 6 | NA18939.hp1 NA18949.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+810T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699040 | ||||||
chr4:105699348
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0105a0001c0001t0001g0106 | 4 | HG01928.hp1 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+502A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699348 | ||||||
chr4:105699370
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.156+480G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699370 | ||||||
chr4:105699468
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0173 | 7 | NA18993.hp2 NA19007.hp1 NA19060.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+382A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699468 | ||||||
chr4:105699601
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.156+249C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699601 | ||||||
chr4:105699669
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.156+181G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699669 | ||||||
chr4:105699757
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.156+93G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699757 | ||||||
chr4:105699808
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0187a0001c0001t0001g0193 | 4 | NA18990.hp1 NA18994.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+42C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699808 | ||||||
chr4:105699826
|
C | T | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+24G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699826 | ||||||
chr4:105700100
|
A | G | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-86T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700100 | ||||||
chr4:105700101
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-9-87A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700101 | ||||||
chr4:105700351
|
G | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-337C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700351 | ||||||
chr4:105700361
|
C | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0189others(3): Show | 6 | HG01070.hp1 HG02630.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-347G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700361 | ||||||
chr4:105700486
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(51): Show | 84 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-9-472A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700486 | ||||||
chr4:105700553
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-9-539T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700553 | ||||||
chr4:105700589
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0157 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-9-575A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700589 | ||||||
chr4:105700706
|
A | AAC | 20 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0078others(17): Show | 23 | HG01256.hp2 HG01928.hp1 HG02129.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-694_-9-693dupGT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACAC | 8 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0057others(5): Show | 13 | HG01069.hp2 HG01167.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-696_-9-693dupGT others(2): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACAC | 5 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 6 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-698_-9-693dupGT others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(1): Show |
18 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0027others(15): Show | 37 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.-9-700_-9-693dupGT others(6): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(3): Show |
16 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0025others(13): Show | 30 | HG00741.hp1 HG01069.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9-702_-9-693dupGT others(8): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(5): Show |
13 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0054others(10): Show | 18 | HG00639.hp1 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-704_-9-693dupGT others(10): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(7): Show |
11 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0062others(8): Show | 14 | HG00735.hp2 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-706_-9-693dupGT others(12): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(9): Show |
8 | a0001c0001t0001g0081a0001c0001t0001g0090a0001c0001t0001g0180others(5): Show | 8 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-708_-9-693dupGT others(14): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(11): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0178others(4): Show | 9 | HG00280.hp2 HG02015.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-710_-9-693dupGT others(16): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(13): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 6 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-712_-9-693dupGT others(18): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(15): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0177 | 2 | HG02523.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-9-714_-9-693dupGT others(20): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | AACACACA others(17): Show |
1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9-716_-9-693dupGT others(22): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0048 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-9-693_-9-692insGT others(9): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0043 | 2 | NA18994.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-9-693_-9-692insGT others(15): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9-693_-9-692insGT others(17): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
A | ACACACAC others(18): Show |
1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-9-693_-9-692insGT others(23): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700706
|
AACACAC | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0158 | 3 | HG02615.hp1 HG02818.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-9-698_-9-693delGT others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | ||||||
chr4:105700861
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-9-847G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700861 | ||||||
chr4:105701033
|
T | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-1019A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701033 | ||||||
chr4:105701233
|
CT | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0015others(63): Show | 86 | HG00280.hp2 HG00408.hp2 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.-9-1220delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701233 | ||||||
chr4:105701233
|
CTT | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 67 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-9-1221_-9-1220del others(2): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701233 | ||||||
chr4:105701353
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-9-1339A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701353 | ||||||
chr4:105701416
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-9-1402A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701416 | ||||||
chr4:105701473
|
A | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0178a0001c0001t0001g0179others(3): Show | 8 | HG00280.hp2 HG01081.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1459T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701473 | ||||||
chr4:105701603
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-9-1589G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701603 | ||||||
chr4:105701880
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-10+1768G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701880 | ||||||
chr4:105702066
|
A | G | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1582T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702066 | ||||||
chr4:105702130
|
C | CT | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0034others(24): Show | 31 | HG00597.hp1 HG01346.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.-10+1517dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702130 | ||||||
chr4:105702130
|
C | CTT | 8 | a0001c0001t0001g0070a0001c0002t0001g0009a0001c0002t0001g0019others(5): Show | 14 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+1516_-10+1517d others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702130 | ||||||
chr4:105702130
|
CT | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0084others(4): Show | 7 | HG01167.hp1 HG02155.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+1517delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702130 | ||||||
chr4:105702180
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10+1468C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702180 | ||||||
chr4:105702285
|
G | A | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1363C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702285 | ||||||
chr4:105702425
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0105a0001c0001t0001g0106 | 4 | HG01928.hp1 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+1223G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702425 | ||||||
chr4:105702464
|
A | T | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1184T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702464 | ||||||
chr4:105702517
|
A | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1131T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702517 | ||||||
chr4:105702879
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-10+769T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702879 | ||||||
chr4:105703128
|
C | T | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+520G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703128 | ||||||
chr4:105703309
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-10+339T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703309 | ||||||
chr4:105703345
|
T | C | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+303A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703345 | ||||||
chr4:105703372
|
C | T | 5 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+276G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703372 | ||||||
chr4:105703415
|
A | T | 1 | a0001c0001t0001g0021 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-10+233T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703415 | ||||||
chr4:105703576
|
C | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG02257.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-10+72G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703576 | ||||||
chr4:105703614
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10+34T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703614 | ||||||
chr4:105703643
|
C | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-10+5G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703643 | ||||||
chr4:105703969
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-171-160A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105703969 | ||||||
chr4:105704014
|
C | CT | 20 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0083others(17): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-171-206dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704014 | ||||||
chr4:105704015
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-171-206A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704015 | ||||||
chr4:105704106
|
G | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(92): Show | 142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-171-297C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704106 | ||||||
chr4:105704223
|
G | A | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-414C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704223 | ||||||
chr4:105704250
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-171-441T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704250 | ||||||
chr4:105704253
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-171-444G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704253 | ||||||
chr4:105704305
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-171-496T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704305 | ||||||
chr4:105704479
|
G | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.-171-670C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704479 | ||||||
chr4:105704917
|
A | T | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0069others(9): Show | 14 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-1108T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704917 | ||||||
chr4:105705026
|
T | G | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-171-1217A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705026 | ||||||
chr4:105705027
|
C | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016others(19): Show | 35 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.-171-1218G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705027 | ||||||
chr4:105705115
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-171-1306C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705115 | ||||||
chr4:105705218
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-171-1409A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705218 | ||||||
chr4:105705232
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0130a0001c0001t0001g0131 | 4 | NA18971.hp1 NA19003.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-171-1423G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705232 | ||||||
chr4:105705359
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-171-1550T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705359 | ||||||
chr4:105705406
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0129 | 3 | NA18747.hp1 NA19007.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-171-1597T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705406 | ||||||
chr4:105705513
|
GCCAAAAA others(9): Show |
G | 4 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0065others(1): Show | 5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-1720_-171-170 others(20): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705513 | ||||||
chr4:105705712
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-171-1903A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705712 | ||||||
chr4:105705728
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-171-1919T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705728 | ||||||
chr4:105706244
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-172+2394T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706244 | ||||||
chr4:105706254
|
C | CT | 8 | a0001c0001t0001g0080a0001c0001t0001g0124a0001c0001t0001g0126others(5): Show | 8 | HG02523.hp1 HG02965.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-172+2383dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706254 | ||||||
chr4:105706254
|
CT | C | 10 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 11 | HG01257.hp1 HG02055.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-172+2383delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706254 | ||||||
chr4:105706254
|
CTT | C | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-172+2382_-172+238 others(6): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706254 | ||||||
chr4:105706410
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-172+2228C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706410 | ||||||
chr4:105706469
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-172+2169G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706469 | ||||||
chr4:105706532
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-172+2106C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706532 | ||||||
chr4:105706553
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-172+2085T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706553 | ||||||
chr4:105706618
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-172+2020C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706618 | ||||||
chr4:105706652
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-172+1986G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706652 | ||||||
chr4:105706681
|
C | T | 19 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.-172+1957G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706681 | ||||||
chr4:105706696
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-172+1942G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706696 | ||||||
chr4:105706791
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(16): Show | 36 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.-172+1847G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706791 | ||||||
chr4:105706792
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-172+1846C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706792 | ||||||
chr4:105706807
|
A | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 10 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+1831T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706807 | ||||||
chr4:105707065
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 10 | HG02109.hp2 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+1573T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707065 | ||||||
chr4:105707223
|
G | T | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0069others(9): Show | 14 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+1415C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707223 | ||||||
chr4:105707316
|
A | AT | 16 | a0001c0001t0001g0028a0001c0001t0001g0105a0001c0001t0001g0106others(13): Show | 23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-172+1321dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707316 | ||||||
chr4:105707316
|
AT | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0102others(8): Show | 18 | HG00673.hp1 HG01069.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-172+1321delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707316 | ||||||
chr4:105707500
|
A | T | 1 | a0001c0001t0004g0010 | 3 | NA18952.hp2 NA18953.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-172+1138T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707500 | ||||||
chr4:105707798
|
C | T | 9 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0020others(6): Show | 15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-172+840G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707798 | ||||||
chr4:105707852
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(92): Show | 142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-172+786C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707852 | ||||||
chr4:105708089
|
A | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 83 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-172+549T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708089 | ||||||
chr4:105708140
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-172+498A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708140 | ||||||
chr4:105708410
|
A | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016others(19): Show | 35 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.-172+228T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708410 | ||||||
chr4:105708481
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-172+157T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708481 |