geneid | 54766 |
---|---|
ensemblid | ENSG00000137707.14 |
hgncid | 13862 |
symbol | BTG4 |
name | BTG anti-proliferation factor 4 |
refseq_nuc | NM_001367975.1 |
refseq_prot | NP_001354904.1 |
ensembl_nuc | ENST00000692032.1 |
ensembl_prot | ENSP00000509850.1 |
mane_status | MANE Select |
chr | chr11 |
start | 111494815 |
end | 111512386 |
strand | - |
ver | v1.2 |
region | chr11:111494815-111512386 |
region5000 | chr11:111489815-111517386 |
regionname0 | BTG4_chr11_111494815_111512386 |
regionname5000 | BTG4_chr11_111489815_111517386 |
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 | 229 | 350 | 95 | 67 | 144 | 10 | 32 | 122 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0002 | 0/0 | 228 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0003 | 0/0 | 229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0004 | 0/0 | 229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
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 | 0/1 | 690 | 339 | 89 | 63 | 144 | 10 | 32 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
c0002 | 1/0 | 690 | 11 | 6 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
c0003 | 0/0 | 690 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
c0004 | 0/0 | 690 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
c0005 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
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 | 553 | 322 | 68 | 65 | 146 | 10 | 31 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
t0002 | 0/0 | 553 | 10 | 9 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
t0003 | 0/0 | 553 | 9 | 6 | 2 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
t0004 | 0/0 | 553 | 8 | 8 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
t0005 | 0/0 | 553 | 5 | 5 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 74 | 4 | 9 | 48 | 2 | 10 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0002 | 0/0 | 56 | 4 | 13 | 30 | 2 | 7 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0004 | 0/0 | 8 | 4 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0006 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0010 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0011 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0012 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
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 | 0/1 | 690 | 339 | 89 | 63 | 144 | 10 | 32 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0001c0002 | 1/0 | 690 | 11 | 6 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0002c0003 | 0/0 | 690 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0003c0005 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0004c0004 | 0/0 | 690 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1242 | 307 | 61 | 60 | 144 | 10 | 31 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0001c0001t0002 | 0/0 | 1242 | 10 | 9 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0001c0001t0003 | 0/0 | 1242 | 9 | 6 | 2 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0001c0001t0004 | 0/0 | 1242 | 8 | 8 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0001c0001t0005 | 0/0 | 1242 | 5 | 5 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0001c0002t0001 | 1/0 | 1242 | 11 | 6 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0002c0003t0001 | 0/0 | 1242 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0003c0005t0001 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
a0004c0004t0001 | 0/0 | 1242 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | copy fasta | chr11 | 111489815 | 111517386 |
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 | 0/1 | 74 | 4 | 9 | 48 | 2 | 10 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0002 | 0/0 | 56 | 4 | 13 | 30 | 2 | 7 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0006 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0002g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0012 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0002t0001g0004 | 0/0 | 8 | 4 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0002t0001g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0002c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0003c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0004c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02293 | hp1 | a0004 | c0004 | t0001 | g0073 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02895 | hp2 | a0003 | c0005 | t0001 | g0097 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18970 | hp1 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0095 | REF | REF | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111495140
|
G | A | 1 | a0002 | 2 | NA18970.hp1 NA18990.hp1 |
stop_gained | HIGH | c.685C>T | p.Arg229* | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 917/1242 | 685/690 | 229/229 | chr11 | 111495140 | ||
chr11:111495179
|
T | C | 1 | a0003 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.646A>G | p.Met216Val | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 878/1242 | 646/690 | 216/229 | chr11 | 111495179 | ||
chr11:111498719
|
C | T | 1 | a0004 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.58G>A | p.Asp20Asn | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/5 | 290/1242 | 58/690 | 20/229 | chr11 | 111498719 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111497322
|
G | T | 4 | a0001c0001a0002c0003a0003c0005others(1): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
synonymous_variant | LOW | c.399C>A | p.Ala133Ala | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/5 | 631/1242 | 399/690 | 133/229 | chr11 | 111497322 | ||
chr11:111498684
|
T | C | 1 | a0003c0005 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.93A>G | p.Ala31Ala | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/5 | 325/1242 | 93/690 | 31/229 | chr11 | 111498684 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111494934
|
C | T | 1 | a0001c0001t0003 | 9 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*201G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 201 | chr11 | 111494934 | |||||
chr11:111495134
|
G | A | 1 | a0001c0001t0005 | 5 | HG02630.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 1 | chr11 | 111495134 | |||||
chr11:111512223
|
G | A | 1 | a0001c0001t0002 | 10 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/5 | 13447 | chr11 | 111512223 | |||||
chr11:111512347
|
C | T | 1 | a0001c0001t0004 | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-193G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/5 | 13571 | chr11 | 111512347 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111495707
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.511-393A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495707 | ||||||
chr11:111495735
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(30): Show | 111 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.511-421A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495735 | ||||||
chr11:111495737
|
G | T | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-423C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495737 | ||||||
chr11:111495833
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.511-519C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495833 | ||||||
chr11:111495986
|
G | C | 1 | a0001c0001t0003g0055 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.511-672C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495986 | ||||||
chr11:111496067
|
A | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(29): Show | 110 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.511-753T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496067 | ||||||
chr11:111496119
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(39): Show | 125 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.511-805C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496119 | ||||||
chr11:111496299
|
T | C | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.510+912A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496299 | ||||||
chr11:111496331
|
T | G | 1 | a0001c0001t0001g0027 | 2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510+880A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496331 | ||||||
chr11:111496358
|
T | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(39): Show | 125 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.510+853A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496358 | ||||||
chr11:111496466
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.510+745T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496466 | ||||||
chr11:111496477
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+734T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496477 | ||||||
chr11:111496504
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.510+707C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496504 | ||||||
chr11:111496758
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.510+453A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496758 | ||||||
chr11:111496892
|
G | GA | 10 | a0001c0001t0001g0039a0001c0001t0001g0063a0001c0001t0001g0075others(7): Show | 21 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.510+318dupT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496892 | ||||||
chr11:111496892
|
G | GAA | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.510+317_510+318dup others(2): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496892 | ||||||
chr11:111496892
|
G | GAAA | 8 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0026others(5): Show | 19 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+316_510+318dup others(3): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496892 | ||||||
chr11:111497164
|
G | T | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0064others(1): Show | 4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+47C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111497164 | ||||||
chr11:111497444
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0003g0012a0001c0001t0003g0055 | 6 | HG00733.hp1 HG01099.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-35C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497444 | ||||||
chr11:111497522
|
A | G | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.312-113T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497522 | ||||||
chr11:111497555
|
T | A | 1 | a0001c0001t0004g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.312-146A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497555 | ||||||
chr11:111497571
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.312-162T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497571 | ||||||
chr11:111497819
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.311+179T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497819 | ||||||
chr11:111497866
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0031 | 5 | HG00733.hp2 HG02148.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+132T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497866 | ||||||
chr11:111497966
|
TCA | T | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.311+30_311+31delTG | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497966 | ||||||
chr11:111498368
|
A | G | 4 | a0001c0001t0004g0009a0001c0001t0004g0046a0001c0001t0004g0047others(1): Show | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.174-233T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498368 | ||||||
chr11:111498407
|
G | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.173+197C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498407 | ||||||
chr11:111498469
|
C | T | 1 | a0001c0001t0001g0030 | 2 | NA18952.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.173+135G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498469 | ||||||
chr11:111498570
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.173+34C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498570 | ||||||
chr11:111499026
|
G | GA | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 12 | HG01928.hp1 HG01928.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-225dupT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499026 | ||||||
chr11:111499027
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0070 | 8 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-225T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499027 | ||||||
chr11:111499034
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-232T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499034 | ||||||
chr11:111499630
|
T | C | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-828A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499630 | ||||||
chr11:111499690
|
C | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(38): Show | 126 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.-26-888G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499690 | ||||||
chr11:111499702
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-26-900C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499702 | ||||||
chr11:111499812
|
C | A | 1 | a0001c0001t0001g0016 | 4 | HG02965.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-1010G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499812 | ||||||
chr11:111499867
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-26-1065G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499867 | ||||||
chr11:111499870
|
G | A | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-1068C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499870 | ||||||
chr11:111499877
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-26-1075G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499877 | ||||||
chr11:111499970
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(28): Show | 104 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-26-1168G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499970 | ||||||
chr11:111500141
|
C | CA | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0054others(2): Show | 7 | HG02055.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-1340dupT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500141 | ||||||
chr11:111500147
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-26-1345T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500147 | ||||||
chr11:111500147
|
AT | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0003g0062 | 3 | NA19011.hp2 NA19043.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-26-1346delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500147 | ||||||
chr11:111500148
|
T | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-26-1346A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500148 | ||||||
chr11:111500179
|
T | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-1377A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500179 | ||||||
chr11:111500434
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-1632C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500434 | ||||||
chr11:111500543
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-26-1741G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500543 | ||||||
chr11:111500679
|
C | CT | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(55): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-26-1878dupA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500679 | ||||||
chr11:111500679
|
C | CTT | 6 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0026others(3): Show | 18 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-1879_-26-1878d others(4): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500679 | ||||||
chr11:111500679
|
CT | C | 12 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0063others(9): Show | 23 | HG00733.hp1 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-26-1878delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500679 | ||||||
chr11:111500752
|
TCCCTC | T | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-1955_-26-1951d others(7): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500752 | ||||||
chr11:111500780
|
A | G | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-1978T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500780 | ||||||
chr11:111500948
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26-2146C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500948 | ||||||
chr11:111501068
|
AG | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0105a0001c0001t0001g0115 | 5 | HG01255.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-2267delC | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501068 | ||||||
chr11:111501092
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0122 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-26-2290C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501092 | ||||||
chr11:111501136
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26-2334G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501136 | ||||||
chr11:111501256
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26-2454G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501256 | ||||||
chr11:111501340
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0005g0089 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-26-2538G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501340 | ||||||
chr11:111501381
|
A | T | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-2579T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501381 | ||||||
chr11:111501519
|
AATAG | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0019 | 10 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26-2721_-26-2718d others(6): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501519 | ||||||
chr11:111501520
|
A | C | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0064others(1): Show | 4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-2718T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501520 | ||||||
chr11:111501580
|
A | C | 1 | a0001c0001t0001g0043 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-26-2778T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501580 | ||||||
chr11:111501713
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-26-2911A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501713 | ||||||
chr11:111501774
|
C | T | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-2972G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501774 | ||||||
chr11:111502074
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 103 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-26-3272G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502074 | ||||||
chr11:111502077
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-26-3275A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502077 | ||||||
chr11:111502088
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-26-3286C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502088 | ||||||
chr11:111502120
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-3318G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502120 | ||||||
chr11:111502138
|
AT | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0082others(3): Show | 11 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-3337delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502138 | ||||||
chr11:111502150
|
TC | T | 4 | a0001c0001t0004g0009a0001c0001t0004g0046a0001c0001t0004g0047others(1): Show | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-3349delG | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502150 | ||||||
chr11:111502195
|
C | T | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-3393G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502195 | ||||||
chr11:111502301
|
G | A | 1 | a0001c0001t0001g0017 | 4 | NA18942.hp1 NA18957.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-3499C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502301 | ||||||
chr11:111502323
|
T | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-3521A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502323 | ||||||
chr11:111502329
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-3527A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502329 | ||||||
chr11:111502348
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-26-3546C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502348 | ||||||
chr11:111502378
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(34): Show | 115 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-26-3576T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502378 | ||||||
chr11:111502396
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0121 | 7 | NA18963.hp2 NA18968.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-3594T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502396 | ||||||
chr11:111502420
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0087 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-26-3618G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502420 | ||||||
chr11:111502487
|
G | A | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-3685C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502487 | ||||||
chr11:111502527
|
T | G | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0064others(1): Show | 4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-3725A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502527 | ||||||
chr11:111502637
|
C | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0122 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-26-3835G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502637 | ||||||
chr11:111503111
|
C | T | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-4309G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503111 | ||||||
chr11:111503214
|
C | A | 4 | a0001c0001t0004g0009a0001c0001t0004g0046a0001c0001t0004g0047others(1): Show | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-4412G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503214 | ||||||
chr11:111503379
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-26-4577G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503379 | ||||||
chr11:111503381
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-26-4579C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503381 | ||||||
chr11:111503439
|
A | G | 1 | a0001c0001t0001g0021 | 3 | HG01256.hp1 HG01258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-26-4637T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503439 | ||||||
chr11:111503466
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0087 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-26-4664A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503466 | ||||||
chr11:111503580
|
TC | T | 1 | a0001c0001t0001g0010 | 5 | HG01257.hp2 HG01258.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-4779delG | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503580 | ||||||
chr11:111503609
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(38): Show | 126 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.-26-4807G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503609 | ||||||
chr11:111503664
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-26-4862T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503664 | ||||||
chr11:111503710
|
T | G | 4 | a0001c0001t0004g0009a0001c0001t0004g0046a0001c0001t0004g0047others(1): Show | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-4908A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503710 | ||||||
chr11:111503711
|
T | C | 6 | a0001c0001t0003g0012a0001c0001t0003g0055a0001c0001t0003g0061others(3): Show | 9 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26-4909A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503711 | ||||||
chr11:111503770
|
A | G | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0064others(1): Show | 4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-4968T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503770 | ||||||
chr11:111503792
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-4990C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503792 | ||||||
chr11:111503861
|
G | A | 1 | a0001c0001t0003g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-26-5059C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503861 | ||||||
chr11:111503876
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-5074G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503876 | ||||||
chr11:111503905
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-26-5103C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503905 | ||||||
chr11:111503911
|
T | A | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5109A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503911 | ||||||
chr11:111504059
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-26-5257G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504059 | ||||||
chr11:111504105
|
C | A | 1 | a0003c0005t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-26-5303G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504105 | ||||||
chr11:111504383
|
G | T | 1 | a0001c0001t0005g0035 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-26-5581C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504383 | ||||||
chr11:111504412
|
A | G | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5610T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504412 | ||||||
chr11:111504575
|
C | A | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5773G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504575 | ||||||
chr11:111504724
|
A | C | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5922T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504724 | ||||||
chr11:111504806
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-26-6004C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504806 | ||||||
chr11:111504845
|
T | G | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-6043A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504845 | ||||||
chr11:111505062
|
A | C | 2 | a0001c0001t0001g0088a0001c0001t0005g0089 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-26-6260T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505062 | ||||||
chr11:111505382
|
C | G | 1 | a0001c0001t0001g0020 | 3 | HG00733.hp2 HG02148.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-26-6580G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505382 | ||||||
chr11:111505393
|
A | T | 1 | a0001c0001t0001g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26-6591T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505393 | ||||||
chr11:111505540
|
C | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-27+6641G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505540 | ||||||
chr11:111505617
|
CGAAG | C | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+6560_-27+6563d others(6): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505617 | ||||||
chr11:111505618
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0005g0089 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-27+6563C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505618 | ||||||
chr11:111505623
|
T | A | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+6558A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505623 | ||||||
chr11:111505740
|
T | A | 1 | a0001c0001t0001g0024 | 3 | HG01109.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-27+6441A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505740 | ||||||
chr11:111505828
|
T | A | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6353A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505828 | ||||||
chr11:111505829
|
T | C | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6352A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505829 | ||||||
chr11:111505830
|
T | A | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6351A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505830 | ||||||
chr11:111505831
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6350G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505831 | ||||||
chr11:111505832
|
T | A | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6349A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505832 | ||||||
chr11:111505835
|
G | A | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6346C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505835 | ||||||
chr11:111505838
|
G | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6343C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505838 | ||||||
chr11:111505840
|
A | T | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6341T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505840 | ||||||
chr11:111505953
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0084 | 4 | NA18955.hp1 NA18991.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+6228A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505953 | ||||||
chr11:111506066
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0005g0089 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-27+6115G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506066 | ||||||
chr11:111506101
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-27+6080G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506101 | ||||||
chr11:111506163
|
A | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-27+6018T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506163 | ||||||
chr11:111506210
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27+5971T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506210 | ||||||
chr11:111506264
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0003g0061others(4): Show | 8 | HG02145.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+5917A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506264 | ||||||
chr11:111506287
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+5894A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506287 | ||||||
chr11:111506510
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-27+5671T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506510 | ||||||
chr11:111506585
|
A | T | 1 | a0001c0001t0001g0014 | 4 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+5596T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506585 | ||||||
chr11:111506769
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0087 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-27+5412T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506769 | ||||||
chr11:111506921
|
C | CTATAGA | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+5254_-27+5259d others(8): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506921 | ||||||
chr11:111507033
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-27+5148C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507033 | ||||||
chr11:111507226
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4955G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507226 | ||||||
chr11:111507363
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27+4818A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507363 | ||||||
chr11:111507562
|
T | C | 1 | a0001c0002t0001g0037 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-27+4619A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507562 | ||||||
chr11:111507671
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-27+4510A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507671 | ||||||
chr11:111507793
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-27+4388G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507793 | ||||||
chr11:111507979
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-27+4202T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507979 | ||||||
chr11:111508032
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+4149T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508032 | ||||||
chr11:111508097
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0058 | 6 | HG00438.hp2 HG02165.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+4084C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508097 | ||||||
chr11:111508202
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-27+3979A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508202 | ||||||
chr11:111508311
|
C | T | 8 | a0001c0001t0001g0039a0001c0001t0003g0012a0001c0001t0003g0055others(5): Show | 12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+3870G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508311 | ||||||
chr11:111508329
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(28): Show | 104 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-27+3852G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508329 | ||||||
chr11:111508346
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-27+3835A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508346 | ||||||
chr11:111508366
|
C | CT | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.-27+3814dupA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508366 | ||||||
chr11:111508747
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0019 | 10 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27+3434T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508747 | ||||||
chr11:111508753
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-27+3428T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508753 | ||||||
chr11:111508841
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-27+3340A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508841 | ||||||
chr11:111508926
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-27+3255A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508926 | ||||||
chr11:111509108
|
A | G | 8 | a0001c0001t0001g0039a0001c0001t0003g0012a0001c0001t0003g0055others(5): Show | 12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+3073T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509108 | ||||||
chr11:111509134
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27+3047T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509134 | ||||||
chr11:111509178
|
G | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0092a0001c0001t0003g0012others(6): Show | 13 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-27+3003C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509178 | ||||||
chr11:111509179
|
C | A | 8 | a0001c0001t0001g0039a0001c0001t0003g0012a0001c0001t0003g0055others(5): Show | 12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+3002G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509179 | ||||||
chr11:111509191
|
T | A | 8 | a0001c0001t0001g0039a0001c0001t0003g0012a0001c0001t0003g0055others(5): Show | 12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2990A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509191 | ||||||
chr11:111509192
|
T | G | 8 | a0001c0001t0001g0039a0001c0001t0003g0012a0001c0001t0003g0055others(5): Show | 12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2989A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509192 | ||||||
chr11:111509193
|
T | A | 8 | a0001c0001t0001g0039a0001c0001t0003g0012a0001c0001t0003g0055others(5): Show | 12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2988A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509193 | ||||||
chr11:111509254
|
C | G | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-27+2927G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509254 | ||||||
chr11:111509273
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-27+2908C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509273 | ||||||
chr11:111509305
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27+2876A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509305 | ||||||
chr11:111509700
|
AAAAAAC | A | 5 | a0001c0001t0001g0116a0001c0001t0004g0009a0001c0001t0004g0046others(2): Show | 9 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27+2475_-27+2480d others(8): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509700 | ||||||
chr11:111509821
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2360T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509821 | ||||||
chr11:111509823
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2358G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509823 | ||||||
chr11:111509827
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2354C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509827 | ||||||
chr11:111509831
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2350C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509831 | ||||||
chr11:111509832
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2349T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509832 | ||||||
chr11:111509832
|
A | T | 2 | a0001c0001t0001g0063a0001c0001t0003g0064 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-27+2349T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509832 | ||||||
chr11:111509833
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2348A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509833 | ||||||
chr11:111509836
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2345A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509836 | ||||||
chr11:111509840
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2341A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509840 | ||||||
chr11:111509844
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2337A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509844 | ||||||
chr11:111509846
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2335A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509846 | ||||||
chr11:111509848
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2333A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509848 | ||||||
chr11:111509855
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2326C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509855 | ||||||
chr11:111509856
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2325C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509856 | ||||||
chr11:111509863
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2318A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509863 | ||||||
chr11:111509867
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2314A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509867 | ||||||
chr11:111509871
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2310G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509871 | ||||||
chr11:111509872
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2309A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509872 | ||||||
chr11:111509873
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2308G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509873 | ||||||
chr11:111509874
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2307G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509874 | ||||||
chr11:111509874
|
CA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-27+2306delT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509874 | ||||||
chr11:111509876
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2305T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509876 | ||||||
chr11:111509879
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2302C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509879 | ||||||
chr11:111509880
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2301A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509880 | ||||||
chr11:111509882
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2299A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509882 | ||||||
chr11:111509883
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2298G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509883 | ||||||
chr11:111509885
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2296T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509885 | ||||||
chr11:111509890
|
T | C | 1 | a0003c0005t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+2291A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509890 | ||||||
chr11:111509891
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2290A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509891 | ||||||
chr11:111509897
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2284G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509897 | ||||||
chr11:111509904
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2277G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509904 | ||||||
chr11:111509911
|
C | CT | 6 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 7 | HG00609.hp1 HG02976.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+2269dupA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509911 | ||||||
chr11:111509911
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2270G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509911 | ||||||
chr11:111509911
|
CT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0096others(2): Show | 12 | HG00140.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2269delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509911 | ||||||
chr11:111509975
|
G | A | 1 | a0003c0005t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+2206C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509975 | ||||||
chr11:111510004
|
C | T | 1 | a0001c0001t0001g0041 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-27+2177G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510004 | ||||||
chr11:111510057
|
G | T | 1 | a0001c0001t0001g0056 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-27+2124C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510057 | ||||||
chr11:111510064
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0055 | 5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+2117T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510064 | ||||||
chr11:111510205
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-27+1976G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510205 | ||||||
chr11:111510206
|
G | A | 1 | a0001c0001t0001g0025 | 3 | NA18946.hp1 NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-27+1975C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510206 | ||||||
chr11:111510237
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-27+1944G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510237 | ||||||
chr11:111510449
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0049 | 3 | NA18957.hp1 NA18971.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-27+1732A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510449 | ||||||
chr11:111510568
|
G | A | 2 | a0001c0001t0001g0039a0003c0005t0001g0097 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+1613C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510568 | ||||||
chr11:111510760
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-27+1421C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510760 | ||||||
chr11:111511093
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-27+1088A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511093 | ||||||
chr11:111511278
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27+903A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511278 | ||||||
chr11:111511328
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-27+853G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511328 | ||||||
chr11:111511455
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-27+726A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511455 | ||||||
chr11:111511520
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27+661A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511520 | ||||||
chr11:111511668
|
A | C | 1 | a0002c0003t0001g0040 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-27+513T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511668 | ||||||
chr11:111511789
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-27+392T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511789 | ||||||
chr11:111511840
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(30): Show | 111 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.-27+341A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511840 | ||||||
chr11:111511851
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+330A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511851 | ||||||
chr11:111511895
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-27+286A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511895 | ||||||
chr11:111511900
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-27+281T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511900 | ||||||
chr11:111511901
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0121 | 5 | NA18963.hp2 NA18968.hp2 NA19080.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+280A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511901 | ||||||
chr11:111511914
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+267T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511914 | ||||||
chr11:111511930
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-27+251A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511930 |