geneid | 2959 |
---|---|
ensemblid | ENSG00000137947.12 |
hgncid | 4648 |
symbol | GTF2B |
name | general transcription factor IIB |
refseq_nuc | NM_001514.6 |
refseq_prot | NP_001505.1 |
ensembl_nuc | ENST00000370500.10 |
ensembl_prot | ENSP00000359531.5 |
mane_status | MANE Select |
chr | chr1 |
start | 88852633 |
end | 88891567 |
strand | - |
ver | v1.2 |
region | chr1:88852633-88891567 |
region5000 | chr1:88847633-88896567 |
regionname0 | GTF2B_chr1_88852633_88891567 |
regionname5000 | GTF2B_chr1_88847633_88896567 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 951 | 355 | 83 | 68 | 154 | 12 | 37 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
c0002 | 1/0 | 951 | 11 | 10 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
c0003 | 0/0 | 951 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
c0004 | 0/0 | 951 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
c0005 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 649 | 311 | 56 | 63 | 142 | 11 | 37 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
t0002 | 0/0 | 656 | 27 | 23 | 3 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
t0003 | 0/0 | 656 | 24 | 7 | 2 | 14 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
t0004 | 0/0 | 649 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
t0005 | 0/0 | 656 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
t0006 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
t0007 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0228 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0315 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 951 | 355 | 83 | 68 | 154 | 12 | 37 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0002 | 1/0 | 951 | 11 | 10 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0003 | 0/0 | 951 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0004 | 0/0 | 951 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0002c0005 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1599 | 300 | 46 | 63 | 142 | 11 | 37 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0001t0002 | 0/0 | 1606 | 23 | 20 | 3 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0001t0003 | 0/0 | 1606 | 22 | 7 | 2 | 12 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0001t0004 | 0/0 | 1599 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0001t0005 | 0/0 | 1606 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0001t0006 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0001t0007 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0002t0001 | 1/0 | 1599 | 11 | 10 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0003t0002 | 0/0 | 1606 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0001c0004t0003 | 0/0 | 1606 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
a0002c0005t0002 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | copy fasta | chr1 | 88847633 | 88896567 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0228 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0005g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0001t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0315 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
a0002c0005t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CDX | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02630 | hp2 | a0001 | c0003 | t0002 | g0172 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0322 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0346 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0320 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0338 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0280 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0341 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0319 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0313 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03516 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03688 | hp1 | a0002 | c0005 | t0002 | g0118 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0095 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19064 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19082 | hp1 | a0001 | c0004 | t0003 | g0176 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ASW | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0331 | EUR | TSI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0345 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0228 | REF | REF | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0315 | REF | REF | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:88860234
|
C | T | 1 | a0002 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.311G>A | p.Arg104Gln | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 4/7 | 379/1599 | 311/951 | 104/316 | chr1 | 88860234 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:88857299
|
G | A | 4 | a0001c0001a0001c0003a0001c0004others(1): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
synonymous_variant | LOW | c.724C>T | p.Leu242Leu | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/7 | 792/1599 | 724/951 | 242/316 | chr1 | 88857299 | ||
chr1:88864008
|
A | G | 1 | a0001c0004 | 2 | NA19064.hp2 NA19082.hp1 |
synonymous_variant | LOW | c.231T>C | p.Asp77Asp | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/7 | 299/1599 | 231/951 | 77/316 | chr1 | 88864008 | ||
chr1:88887298
|
G | A | 1 | a0001c0003 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.87C>T | p.Ala29Ala | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/7 | 155/1599 | 87/951 | 29/316 | chr1 | 88887298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:88852715
|
A | ATAT | 7 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(4): Show | 55 | HG00621.hp2 HG00639.hp1 HG01109.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 497 | chr1 | 88852715 | |||||
chr1:88852788
|
T | A | 1 | a0001c0001t0004 | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*425A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 425 | chr1 | 88852788 | |||||
chr1:88852847
|
T | TAAAG | 2 | a0001c0001t0003a0001c0004t0003 | 24 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*365dupCTTT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 365 | chr1 | 88852847 | |||||
chr1:88852850
|
A | AGAAC | 4 | a0001c0001t0002a0001c0001t0005a0001c0003t0002others(1): Show | 29 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*363insGTTC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 362 | chr1 | 88852850 | |||||
chr1:88853121
|
T | A | 1 | a0001c0001t0005 | 2 | HG02258.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*92A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 92 | chr1 | 88853121 | |||||
chr1:88853121
|
T | C | 1 | a0001c0001t0007 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 92 | chr1 | 88853121 | |||||
chr1:88853156
|
G | C | 1 | a0001c0001t0006 | 2 | HG02809.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*57C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 7/7 | 57 | chr1 | 88853156 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:88853399
|
C | T | 25 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(22): Show | 29 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.818-53G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853399 | ||||||
chr1:88853430
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0154 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.818-84A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853430 | ||||||
chr1:88853431
|
A | G | 1 | a0001c0001t0002g0346 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.818-85T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853431 | ||||||
chr1:88853483
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.818-137T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853483 | ||||||
chr1:88853507
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0047others(1): Show | 4 | HG00140.hp1 HG00642.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-161A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853507 | ||||||
chr1:88853522
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.818-176T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853522 | ||||||
chr1:88853587
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.818-241G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853587 | ||||||
chr1:88853694
|
C | T | 2 | a0001c0001t0001g0311a0001c0001t0001g0318 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.818-348G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853694 | ||||||
chr1:88853752
|
C | T | 24 | a0001c0001t0003g0071a0001c0001t0003g0092a0001c0001t0003g0093others(21): Show | 24 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.818-406G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853752 | ||||||
chr1:88853759
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0198a0001c0001t0001g0206others(4): Show | 7 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.818-413C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853759 | ||||||
chr1:88853801
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.818-455A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853801 | ||||||
chr1:88853934
|
C | G | 51 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(48): Show | 55 | HG00621.hp2 HG00639.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.818-588G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88853934 | ||||||
chr1:88854113
|
T | C | 27 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(24): Show | 31 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.818-767A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854113 | ||||||
chr1:88854138
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.818-792A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854138 | ||||||
chr1:88854229
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0049 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-883A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854229 | ||||||
chr1:88854231
|
T | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0318 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.818-885A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854231 | ||||||
chr1:88854237
|
T | C | 2 | a0001c0002t0001g0280a0001c0002t0001g0312 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.818-891A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854237 | ||||||
chr1:88854261
|
C | T | 3 | a0001c0001t0002g0274a0001c0001t0002g0338a0001c0001t0002g0339 | 3 | HG00639.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.818-915G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854261 | ||||||
chr1:88854353
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.818-1007A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854353 | ||||||
chr1:88854713
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.818-1367G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854713 | ||||||
chr1:88854860
|
A | G | 24 | a0001c0001t0003g0071a0001c0001t0003g0092a0001c0001t0003g0093others(21): Show | 24 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.818-1514T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854860 | ||||||
chr1:88854897
|
ATTAGCTA others(14): Show |
A | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.818-1572_818-1552d others(23): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854897 | ||||||
chr1:88854918
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.818-1572C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854918 | ||||||
chr1:88854994
|
G | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0041others(24): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.818-1648C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88854994 | ||||||
chr1:88855012
|
C | T | 24 | a0001c0001t0003g0071a0001c0001t0003g0092a0001c0001t0003g0093others(21): Show | 24 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.818-1666G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855012 | ||||||
chr1:88855184
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0063a0001c0001t0001g0068others(1): Show | 4 | HG01928.hp2 HG02293.hp2 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-1838C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855184 | ||||||
chr1:88855353
|
G | GT | 3 | a0001c0001t0001g0168a0001c0001t0003g0140a0001c0004t0003g0177 | 3 | HG02040.hp1 HG03139.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.817+1852dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855353 | ||||||
chr1:88855359
|
G | GT | 49 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0024others(46): Show | 53 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.817+1846dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855359 | ||||||
chr1:88855359
|
G | GTT | 8 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0002g0119others(5): Show | 8 | HG02055.hp2 HG02071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.817+1845_817+1846d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855359 | ||||||
chr1:88855359
|
G | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 8 | HG02040.hp1 HG02486.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.817+1847C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855359 | ||||||
chr1:88855359
|
GT | G | 13 | a0001c0001t0001g0160a0001c0001t0001g0272a0001c0001t0002g0017others(10): Show | 14 | HG00639.hp1 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.817+1846delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855359 | ||||||
chr1:88855365
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.817+1841A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855365 | ||||||
chr1:88855430
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.817+1776C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855430 | ||||||
chr1:88855478
|
G | A | 2 | a0001c0001t0002g0336a0001c0001t0002g0337 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.817+1728C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855478 | ||||||
chr1:88855485
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.817+1721A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855485 | ||||||
chr1:88855509
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.817+1697A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855509 | ||||||
chr1:88855559
|
G | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.817+1647C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855559 | ||||||
chr1:88855767
|
A | G | 25 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(22): Show | 29 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.817+1439T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855767 | ||||||
chr1:88855814
|
C | T | 3 | a0001c0001t0002g0082a0001c0003t0002g0013a0001c0003t0002g0172 | 4 | HG02280.hp1 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+1392G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855814 | ||||||
chr1:88855879
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0111a0001c0001t0001g0114others(5): Show | 8 | HG02071.hp2 HG02083.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.817+1327G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855879 | ||||||
chr1:88855880
|
G | A | 24 | a0001c0001t0003g0071a0001c0001t0003g0092a0001c0001t0003g0093others(21): Show | 24 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.817+1326C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855880 | ||||||
chr1:88855929
|
T | C | 5 | a0001c0001t0003g0213a0001c0001t0003g0251a0001c0001t0003g0331others(2): Show | 5 | NA18973.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+1277A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855929 | ||||||
chr1:88855993
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817+1213A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88855993 | ||||||
chr1:88856098
|
C | T | 13 | a0001c0001t0003g0171a0001c0001t0003g0182a0001c0001t0003g0183others(10): Show | 13 | HG01109.hp1 HG02615.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.817+1108G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856098 | ||||||
chr1:88856109
|
A | G | 3 | a0001c0001t0002g0188a0001c0001t0002g0343a0001c0001t0002g0346 | 3 | HG02647.hp1 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.817+1097T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856109 | ||||||
chr1:88856246
|
G | A | 3 | a0001c0001t0002g0188a0001c0001t0002g0343a0001c0001t0002g0346 | 3 | HG02647.hp1 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.817+960C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856246 | ||||||
chr1:88856266
|
CAAAAACA others(7): Show |
C | 5 | a0001c0001t0004g0313a0001c0001t0004g0320a0001c0001t0004g0321others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+926_817+939del others(14): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856266 | ||||||
chr1:88856272
|
C | CA | 72 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0025others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.817+933dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856272 | ||||||
chr1:88856272
|
C | CAA | 52 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.817+932_817+933dup others(2): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856272 | ||||||
chr1:88856272
|
C | CAAA | 26 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0046others(23): Show | 26 | HG00438.hp1 HG02055.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.817+931_817+933dup others(3): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856272 | ||||||
chr1:88856272
|
C | CAAAA | 13 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0027others(10): Show | 14 | HG00438.hp2 HG02165.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.817+930_817+933dup others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856272 | ||||||
chr1:88856272
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0301 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.817+911_817+933del others(23): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856272 | ||||||
chr1:88856276
|
A | AC | 5 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0047others(2): Show | 5 | HG02735.hp1 HG03654.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+929_817+930ins others(1): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856276 | ||||||
chr1:88856278
|
A | C | 25 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(22): Show | 29 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.817+928T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856278 | ||||||
chr1:88856278
|
AAAAAAAA others(6): Show |
A | 5 | a0001c0001t0001g0003a0001c0001t0001g0097a0001c0001t0001g0101others(2): Show | 7 | HG00140.hp2 HG01070.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.817+915_817+927del others(13): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856278 | ||||||
chr1:88856279
|
A | C | 1 | a0001c0001t0001g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.817+927T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856279 | ||||||
chr1:88856279
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0202a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG03098.hp1 HG03453.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.817+915_817+926del others(12): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856279 | ||||||
chr1:88856281
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.817+915_817+924del others(10): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856281 | ||||||
chr1:88856282
|
A | C | 25 | a0001c0001t0001g0091a0001c0001t0003g0071a0001c0001t0003g0092others(22): Show | 25 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.817+924T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856282 | ||||||
chr1:88856283
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.817+923T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856283 | ||||||
chr1:88856283
|
AAAAAAAA others(1): Show |
A | 18 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(15): Show | 22 | HG00639.hp1 HG01169.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.817+915_817+922del others(8): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856283 | ||||||
chr1:88856284
|
AAAAAAAC | A | 7 | a0001c0001t0002g0117a0001c0001t0002g0188a0001c0001t0002g0224others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.817+915_817+921del others(7): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856284 | ||||||
chr1:88856287
|
AAAAC | A | 27 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0091others(24): Show | 27 | HG00621.hp2 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.817+915_817+918del others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856287 | ||||||
chr1:88856290
|
AC | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 63 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.817+915delG | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856290 | ||||||
chr1:88856291
|
C | A | 227 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(224): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.817+915G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856291 | ||||||
chr1:88856354
|
A | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0260 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.817+852T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856354 | ||||||
chr1:88856364
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0063others(9): Show | 14 | HG00733.hp1 HG00738.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.817+842A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856364 | ||||||
chr1:88856444
|
G | GA | 277 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.817+761dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856444 | ||||||
chr1:88856496
|
A | C | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.817+710T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856496 | ||||||
chr1:88856561
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817+645G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856561 | ||||||
chr1:88856704
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | NA18994.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.817+502G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856704 | ||||||
chr1:88856773
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.817+433A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856773 | ||||||
chr1:88856804
|
G | GT | 169 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.817+401dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856804 | ||||||
chr1:88856804
|
G | GTT | 7 | a0001c0001t0001g0031a0001c0001t0001g0050a0001c0001t0001g0062others(4): Show | 7 | HG01069.hp1 HG01358.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.817+400_817+401dup others(2): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856804 | ||||||
chr1:88856804
|
GT | G | 32 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0017others(29): Show | 32 | HG00621.hp2 HG00639.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.817+401delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856804 | ||||||
chr1:88856875
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(330): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.817+331A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856875 | ||||||
chr1:88857048
|
G | A | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.817+158C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88857048 | ||||||
chr1:88857080
|
T | C | 41 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(38): Show | 45 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.817+126A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88857080 | ||||||
chr1:88857126
|
C | T | 46 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(43): Show | 50 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(47): Show |
intron_variant | MODIFIER | c.817+80G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88857126 | ||||||
chr1:88857158
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+48A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88857158 | ||||||
chr1:88857197
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.817+9C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88857197 | ||||||
chr1:88857518
|
C | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.536-31G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857518 | ||||||
chr1:88857657
|
C | A | 2 | a0001c0001t0003g0213a0001c0001t0003g0332 | 2 | NA18973.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.536-170G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857657 | ||||||
chr1:88857691
|
C | CTTTTTTT others(5): Show |
14 | a0001c0001t0001g0049a0001c0001t0001g0147a0001c0001t0001g0227others(11): Show | 14 | HG01081.hp1 HG01081.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.536-205_536-204ins others(12): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857691
|
C | CTTTTTTT others(6): Show |
264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(261): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.536-205_536-204ins others(13): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857691
|
C | CTTTTTTT others(7): Show |
18 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0085others(15): Show | 18 | HG00733.hp1 HG01978.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.536-205_536-204ins others(14): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857691
|
C | CTTTTTTT others(8): Show |
31 | a0001c0001t0001g0091a0001c0001t0001g0334a0001c0001t0002g0002others(28): Show | 35 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.536-205_536-204ins others(15): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857691
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0083a0001c0001t0006g0084a0001c0001t0006g0095 | 3 | HG02809.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.536-205_536-204ins others(16): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857691
|
C | CTTTTTTT others(10): Show |
5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0005g0175others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.536-205_536-204ins others(17): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857691
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.536-205_536-204ins others(18): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857691 | ||||||
chr1:88857703
|
G | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.536-216C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857703 | ||||||
chr1:88857868
|
G | A | 41 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(38): Show | 45 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-381C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857868 | ||||||
chr1:88857870
|
T | C | 41 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(38): Show | 45 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-383A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857870 | ||||||
chr1:88857871
|
G | A | 41 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(38): Show | 45 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-384C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857871 | ||||||
chr1:88857934
|
G | A | 1 | a0001c0001t0002g0339 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.536-447C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857934 | ||||||
chr1:88857950
|
G | C | 1 | a0001c0001t0002g0339 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.536-463C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88857950 | ||||||
chr1:88858044
|
C | T | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.536-557G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858044 | ||||||
chr1:88858168
|
T | C | 20 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0188others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.536-681A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858168 | ||||||
chr1:88858281
|
G | C | 1 | a0001c0001t0002g0339 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.536-794C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858281 | ||||||
chr1:88858397
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.536-910T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858397 | ||||||
chr1:88858552
|
C | G | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.536-1065G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858552 | ||||||
chr1:88858705
|
G | A | 12 | a0001c0001t0001g0282a0001c0001t0001g0288a0001c0001t0001g0289others(9): Show | 12 | HG00741.hp2 HG01346.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.535+1177C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858705 | ||||||
chr1:88858863
|
A | G | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.535+1019T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858863 | ||||||
chr1:88858867
|
C | CT | 18 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0124others(15): Show | 18 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.535+1014dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858867 | ||||||
chr1:88858907
|
G | A | 1 | a0001c0001t0007g0341 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.535+975C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858907 | ||||||
chr1:88858936
|
C | T | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.535+946G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858936 | ||||||
chr1:88858970
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0001g0064 | 3 | HG01358.hp1 HG02258.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.535+912G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858970 | ||||||
chr1:88858971
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.535+911C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88858971 | ||||||
chr1:88859013
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0286 | 2 | NA18960.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.535+869C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859013 | ||||||
chr1:88859014
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0203 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.535+868G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859014 | ||||||
chr1:88859015
|
G | A | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.535+867C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859015 | ||||||
chr1:88859018
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.535+864G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859018 | ||||||
chr1:88859136
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+746C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859136 | ||||||
chr1:88859137
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+745T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859137 | ||||||
chr1:88859138
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+744A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859138 | ||||||
chr1:88859141
|
C | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.535+741G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859141 | ||||||
chr1:88859152
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+730G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859152 | ||||||
chr1:88859155
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+727G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859155 | ||||||
chr1:88859156
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+726T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859156 | ||||||
chr1:88859177
|
T | TTACTACT others(18): Show |
1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.535+704_535+705ins others(25): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859177 | ||||||
chr1:88859204
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.535+678T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859204 | ||||||
chr1:88859244
|
CAAATGTA others(3): Show |
C | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.535+628_535+637del others(10): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859244 | ||||||
chr1:88859308
|
G | C | 1 | a0001c0001t0003g0213 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.535+574C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859308 | ||||||
chr1:88859544
|
G | A | 1 | a0001c0001t0003g0332 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.535+338C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859544 | ||||||
chr1:88859815
|
G | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0090others(2): Show | 5 | HG02647.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+67C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 5/6 | chr1 | 88859815 | ||||||
chr1:88860019
|
G | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0188others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(17): Show |
splice_region_variant&intron_variant | LOW | c.406-8C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 4/6 | chr1 | 88860019 | ||||||
chr1:88860476
|
TAAAGTGT others(8): Show |
T | 1 | a0001c0001t0002g0274 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.259-205_259-191del others(15): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88860476 | ||||||
chr1:88860670
|
CATTAT | C | 6 | a0001c0001t0001g0105a0001c0001t0002g0119a0001c0001t0002g0120others(3): Show | 6 | HG00280.hp1 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-389_259-385del others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88860670 | ||||||
chr1:88860718
|
C | T | 41 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(38): Show | 45 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.259-432G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88860718 | ||||||
chr1:88860742
|
T | C | 20 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0188others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.259-456A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88860742 | ||||||
chr1:88860854
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.259-568A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88860854 | ||||||
chr1:88861016
|
A | G | 9 | a0001c0001t0002g0188a0001c0001t0003g0171a0001c0001t0003g0182others(6): Show | 9 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-730T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861016 | ||||||
chr1:88861036
|
T | G | 3 | a0001c0001t0003g0182a0001c0001t0003g0185a0001c0001t0003g0186 | 3 | HG01109.hp1 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.259-750A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861036 | ||||||
chr1:88861169
|
CAAAAATC others(4): Show |
C | 2 | a0001c0001t0005g0175a0001c0001t0005g0345 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259-894_259-884del others(11): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861169 | ||||||
chr1:88861210
|
ATGAAGAA others(17): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.259-948_259-925del others(24): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861210 | ||||||
chr1:88861315
|
T | C | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.259-1029A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861315 | ||||||
chr1:88861330
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.259-1044A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861330 | ||||||
chr1:88861367
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.259-1081A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861367 | ||||||
chr1:88861380
|
A | G | 3 | a0001c0001t0002g0117a0001c0001t0002g0224a0002c0005t0002g0118 | 3 | HG02451.hp2 HG03579.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.259-1094T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861380 | ||||||
chr1:88861399
|
C | G | 5 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0090others(2): Show | 5 | HG02647.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-1113G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861399 | ||||||
chr1:88861570
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.259-1284C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861570 | ||||||
chr1:88861574
|
G | C | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1288C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861574 | ||||||
chr1:88861578
|
C | T | 1 | a0001c0001t0007g0341 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-1292G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861578 | ||||||
chr1:88861650
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.259-1364C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861650 | ||||||
chr1:88861689
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.259-1403C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88861689 | ||||||
chr1:88862110
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.259-1824T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862110 | ||||||
chr1:88862309
|
G | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0188others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.258+1672C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862309 | ||||||
chr1:88862344
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.258+1637G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862344 | ||||||
chr1:88862411
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0049 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1570G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862411 | ||||||
chr1:88862611
|
C | T | 5 | a0001c0001t0003g0213a0001c0001t0003g0251a0001c0001t0003g0331others(2): Show | 5 | NA18973.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1370G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862611 | ||||||
chr1:88862618
|
C | T | 5 | a0001c0001t0003g0213a0001c0001t0003g0251a0001c0001t0003g0331others(2): Show | 5 | NA18973.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1363G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862618 | ||||||
chr1:88862701
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.258+1280G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862701 | ||||||
chr1:88862702
|
G | A | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.258+1279C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862702 | ||||||
chr1:88862724
|
C | T | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+1257G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862724 | ||||||
chr1:88862791
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.258+1190A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862791 | ||||||
chr1:88862832
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0049 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1149C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862832 | ||||||
chr1:88862897
|
A | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00323.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.258+1084T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862897 | ||||||
chr1:88862963
|
A | G | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258+1018T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88862963 | ||||||
chr1:88863344
|
ATTCTT | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0188others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.258+632_258+636del others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88863344 | ||||||
chr1:88863690
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.258+291A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 3/6 | chr1 | 88863690 | ||||||
chr1:88864205
|
C | CA | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0003g0092others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-92dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864205 | ||||||
chr1:88864237
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0143 | 2 | NA18973.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.125-123C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864237 | ||||||
chr1:88864290
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.125-176C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864290 | ||||||
chr1:88864469
|
G | C | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-355C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864469 | ||||||
chr1:88864631
|
C | T | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-517G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864631 | ||||||
chr1:88864700
|
C | G | 11 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0001t0001g0207others(8): Show | 11 | HG00438.hp2 HG02071.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-586G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864700 | ||||||
chr1:88864777
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125-663C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864777 | ||||||
chr1:88864846
|
G | A | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.125-732C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864846 | ||||||
chr1:88864955
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.125-841C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864955 | ||||||
chr1:88864961
|
CAG | C | 20 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0188others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.125-849_125-848del others(2): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864961 | ||||||
chr1:88864971
|
T | C | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-857A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88864971 | ||||||
chr1:88865117
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.125-1003C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865117 | ||||||
chr1:88865126
|
C | T | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-1012G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865126 | ||||||
chr1:88865197
|
T | A | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-1083A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865197 | ||||||
chr1:88865284
|
C | T | 11 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0001t0001g0207others(8): Show | 11 | HG00438.hp2 HG02071.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-1170G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865284 | ||||||
chr1:88865314
|
G | C | 1 | a0001c0001t0002g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125-1200C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865314 | ||||||
chr1:88865550
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00323.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.125-1436G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865550 | ||||||
chr1:88865632
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0003g0092others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-1518C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865632 | ||||||
chr1:88865799
|
T | C | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-1685A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865799 | ||||||
chr1:88865840
|
C | CA | 14 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0090others(11): Show | 14 | HG00639.hp1 HG01109.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-1727dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865840 | ||||||
chr1:88865840
|
C | CAA | 8 | a0001c0001t0002g0002a0001c0001t0002g0117a0001c0001t0002g0224others(5): Show | 11 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-1728_125-1727d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865840 | ||||||
chr1:88865844
|
A | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0340a0001c0001t0007g0341 | 3 | HG01884.hp2 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.125-1730T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865844 | ||||||
chr1:88865846
|
A | AAAC | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-1733_125-1732i others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865846 | ||||||
chr1:88865846
|
A | C | 11 | a0001c0001t0001g0226a0001c0001t0001g0230a0001c0001t0001g0232others(8): Show | 11 | HG00621.hp2 HG02056.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-1732T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865846 | ||||||
chr1:88865857
|
A | AAAAC | 29 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0219others(26): Show | 29 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-1747_125-1744d others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865857 | ||||||
chr1:88865873
|
C | A | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-1759G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865873 | ||||||
chr1:88865877
|
A | AAAAAC | 17 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(14): Show | 20 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.125-1764_125-1763i others(7): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865877 | ||||||
chr1:88865877
|
A | AC | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-1764_125-1763i others(3): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88865877 | ||||||
chr1:88866130
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.125-2016T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866130 | ||||||
chr1:88866245
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0144 | 2 | NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.125-2131A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866245 | ||||||
chr1:88866248
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.125-2134C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866248 | ||||||
chr1:88866416
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.125-2302A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866416 | ||||||
chr1:88866423
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-2309A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866423 | ||||||
chr1:88866426
|
T | C | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-2312A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866426 | ||||||
chr1:88866467
|
G | T | 1 | a0001c0001t0001g0305 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.125-2353C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866467 | ||||||
chr1:88866482
|
C | T | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.125-2368G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866482 | ||||||
chr1:88866705
|
A | G | 5 | a0001c0001t0004g0313a0001c0001t0004g0320a0001c0001t0004g0321others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-2591T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866705 | ||||||
chr1:88866836
|
G | A | 1 | a0001c0003t0002g0013 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-2722C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866836 | ||||||
chr1:88866858
|
A | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-2744T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866858 | ||||||
chr1:88866916
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.125-2802C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866916 | ||||||
chr1:88866957
|
T | G | 1 | a0001c0001t0001g0290 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.125-2843A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88866957 | ||||||
chr1:88867190
|
C | T | 24 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(21): Show | 28 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.125-3076G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867190 | ||||||
chr1:88867234
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0065 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.125-3120T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867234 | ||||||
chr1:88867248
|
G | A | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-3134C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867248 | ||||||
chr1:88867281
|
C | T | 41 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0002others(38): Show | 45 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.125-3167G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867281 | ||||||
chr1:88867332
|
T | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-3218A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867332 | ||||||
chr1:88867353
|
G | C | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-3239C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867353 | ||||||
chr1:88867367
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.125-3253C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867367 | ||||||
chr1:88867404
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.125-3290T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867404 | ||||||
chr1:88867415
|
T | TG | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-3302dupC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867415 | ||||||
chr1:88867444
|
C | G | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-3330G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867444 | ||||||
chr1:88867548
|
TA | T | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-3435delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867548 | ||||||
chr1:88867775
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3661A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867775 | ||||||
chr1:88867874
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.125-3760G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867874 | ||||||
chr1:88867948
|
A | G | 5 | a0001c0001t0003g0213a0001c0001t0003g0251a0001c0001t0003g0331others(2): Show | 5 | NA18973.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-3834T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88867948 | ||||||
chr1:88868127
|
G | A | 17 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(14): Show | 21 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.125-4013C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868127 | ||||||
chr1:88868165
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.125-4051G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868165 | ||||||
chr1:88868252
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0273 | 2 | HG00741.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.125-4138T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868252 | ||||||
chr1:88868329
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.125-4215A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868329 | ||||||
chr1:88868398
|
A | AATAC | 10 | a0001c0001t0001g0012a0001c0001t0001g0130a0001c0001t0001g0167others(7): Show | 11 | HG02280.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-4285_125-4284i others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868398 | ||||||
chr1:88868493
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.125-4379C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868493 | ||||||
chr1:88868511
|
C | CATGT | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-4398_125-4397i others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868511 | ||||||
chr1:88868533
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.125-4419A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868533 | ||||||
chr1:88868666
|
A | T | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-4552T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868666 | ||||||
chr1:88868740
|
CT | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.125-4627delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868740 | ||||||
chr1:88868845
|
A | C | 47 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0091others(44): Show | 51 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(48): Show |
intron_variant | MODIFIER | c.125-4731T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868845 | ||||||
chr1:88868885
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0276 | 3 | HG02486.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.125-4771T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868885 | ||||||
chr1:88868925
|
C | G | 47 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0091others(44): Show | 51 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(48): Show |
intron_variant | MODIFIER | c.125-4811G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868925 | ||||||
chr1:88869014
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-4900G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869014 | ||||||
chr1:88869050
|
AT | A | 5 | a0001c0001t0004g0313a0001c0001t0004g0320a0001c0001t0004g0321others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-4937delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869050 | ||||||
chr1:88869128
|
AT | A | 20 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0017others(17): Show | 24 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.125-5015delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869128 | ||||||
chr1:88869223
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.125-5109T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869223 | ||||||
chr1:88869511
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.125-5397T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869511 | ||||||
chr1:88869548
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.125-5434G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869548 | ||||||
chr1:88869771
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-5657G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869771 | ||||||
chr1:88869771
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-5657G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869771 | ||||||
chr1:88869840
|
A | G | 24 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(21): Show | 28 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.125-5726T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869840 | ||||||
chr1:88869866
|
G | A | 2 | a0001c0001t0005g0175a0001c0001t0005g0345 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.125-5752C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869866 | ||||||
chr1:88869930
|
C | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0003g0092others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-5816G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869930 | ||||||
chr1:88869959
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 6 | HG02486.hp2 HG02886.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-5845C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88869959 | ||||||
chr1:88870029
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125-5915C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870029 | ||||||
chr1:88870117
|
A | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0225a0001c0001t0001g0229others(1): Show | 4 | HG02027.hp2 NA18981.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-6003T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870117 | ||||||
chr1:88870216
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0035others(5): Show | 8 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-6102C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870216 | ||||||
chr1:88870276
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.125-6162C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870276 | ||||||
chr1:88870564
|
AACT | A | 19 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(16): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-6453_125-6451d others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870564 | ||||||
chr1:88870896
|
C | CT | 14 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0059others(11): Show | 14 | HG00733.hp1 HG01109.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-6783dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870896 | ||||||
chr1:88870896
|
CT | C | 39 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0083others(36): Show | 41 | HG00323.hp2 HG00621.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.125-6783delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870896 | ||||||
chr1:88870896
|
CTT | C | 7 | a0001c0001t0002g0082a0001c0001t0002g0117a0001c0001t0002g0119others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-6784_125-6783d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870896 | ||||||
chr1:88870896
|
CTTT | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-6785_125-6783d others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870896 | ||||||
chr1:88870962
|
T | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.125-6848A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870962 | ||||||
chr1:88871053
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.125-6939G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871053 | ||||||
chr1:88871154
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.125-7040C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871154 | ||||||
chr1:88871569
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125-7455A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871569 | ||||||
chr1:88871621
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.125-7507G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871621 | ||||||
chr1:88871709
|
G | T | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-7595C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871709 | ||||||
chr1:88871719
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.125-7605G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871719 | ||||||
chr1:88871807
|
C | T | 3 | a0001c0001t0003g0213a0001c0001t0003g0332a0001c0001t0003g0333 | 3 | NA18973.hp1 NA18974.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.125-7693G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871807 | ||||||
chr1:88871857
|
G | A | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 15 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-7743C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871857 | ||||||
chr1:88871974
|
C | A | 18 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(15): Show | 22 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.125-7860G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88871974 | ||||||
chr1:88872012
|
C | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.125-7898G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872012 | ||||||
chr1:88872028
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.125-7914G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872028 | ||||||
chr1:88872113
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.125-7999A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872113 | ||||||
chr1:88872174
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01081.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.125-8060G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872174 | ||||||
chr1:88872181
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG02486.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-8067G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872181 | ||||||
chr1:88872182
|
G | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-8068C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872182 | ||||||
chr1:88872299
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-8185G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872299 | ||||||
chr1:88872337
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125-8223G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872337 | ||||||
chr1:88872454
|
A | AT | 6 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02523.hp1 NA18747.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-8341dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872454 | ||||||
chr1:88872455
|
T | TA | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(134): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.125-8342dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | ||||||
chr1:88872455
|
T | TAA | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.125-8343_125-8342d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | ||||||
chr1:88872455
|
T | TAAA | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0102others(6): Show | 11 | HG01358.hp2 HG01884.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.125-8344_125-8342d others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | ||||||
chr1:88872455
|
TA | T | 50 | a0001c0001t0001g0016a0001c0001t0001g0275a0001c0001t0001g0281others(47): Show | 52 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.125-8342delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | ||||||
chr1:88872455
|
TAAAAA | T | 25 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(22): Show | 28 | HG00621.hp2 HG02055.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.125-8346_125-8342d others(7): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | ||||||
chr1:88872455
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | NA18994.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.125-8352_125-8342d others(13): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | ||||||
chr1:88872456
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.125-8342T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872456 | ||||||
chr1:88872629
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-8515A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872629 | ||||||
chr1:88872812
|
G | C | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-8698C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872812 | ||||||
chr1:88872827
|
GTTAC | G | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-8717_125-8714d others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872827 | ||||||
chr1:88872842
|
C | T | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-8728G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872842 | ||||||
chr1:88872871
|
A | G | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-8757T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872871 | ||||||
chr1:88873177
|
A | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.125-9063T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873177 | ||||||
chr1:88873182
|
G | GT | 55 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(52): Show | 57 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.125-9069dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873182 | ||||||
chr1:88873182
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.125-9068C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873182 | ||||||
chr1:88873182
|
GT | G | 30 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0081others(27): Show | 31 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.125-9069delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873182 | ||||||
chr1:88873182
|
GTT | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0117a0001c0001t0002g0347others(1): Show | 7 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-9070_125-9069d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873182 | ||||||
chr1:88873182
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0002g0188a0001c0001t0003g0183 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.125-9080_125-9069d others(14): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873182 | ||||||
chr1:88873188
|
T | G | 1 | a0001c0001t0001g0243 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.125-9074A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873188 | ||||||
chr1:88873191
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-9077A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873191 | ||||||
chr1:88873224
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.125-9110C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873224 | ||||||
chr1:88873229
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.125-9115C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873229 | ||||||
chr1:88873334
|
C | G | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-9220G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873334 | ||||||
chr1:88873337
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.125-9223C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873337 | ||||||
chr1:88873394
|
T | G | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-9280A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873394 | ||||||
chr1:88873440
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.125-9326G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873440 | ||||||
chr1:88873451
|
G | A | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-9337C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873451 | ||||||
chr1:88873566
|
T | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.125-9452A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873566 | ||||||
chr1:88873691
|
C | G | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-9577G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873691 | ||||||
chr1:88873739
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.125-9625G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873739 | ||||||
chr1:88873771
|
C | T | 1 | a0001c0001t0003g0178 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.125-9657G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873771 | ||||||
chr1:88873790
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.125-9676A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873790 | ||||||
chr1:88873847
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.125-9733C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873847 | ||||||
chr1:88873998
|
G | A | 2 | a0001c0001t0002g0336a0001c0001t0002g0337 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.125-9884C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88873998 | ||||||
chr1:88874206
|
C | G | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 13 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-10092G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874206 | ||||||
chr1:88874335
|
G | A | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.125-10221C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874335 | ||||||
chr1:88874372
|
G | GA | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-10259dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874372 | ||||||
chr1:88874474
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.125-10360G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874474 | ||||||
chr1:88874496
|
AATT | A | 3 | a0001c0001t0002g0346a0001c0003t0002g0013a0001c0004t0003g0176 | 4 | HG02922.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-10385_125-1038 others(7): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874496 | ||||||
chr1:88874496
|
AATTT | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0090others(8): Show | 11 | HG00621.hp2 HG02630.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-10386_125-1038 others(8): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874496 | ||||||
chr1:88874497
|
AT | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0107others(16): Show | 20 | HG00408.hp2 HG00544.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.125-10384delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874497 | ||||||
chr1:88874497
|
ATT | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0024others(40): Show | 48 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.125-10385_125-1038 others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874497 | ||||||
chr1:88874497
|
ATTT | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.125-10386_125-1038 others(7): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874497 | ||||||
chr1:88874497
|
ATTTT | A | 31 | a0001c0001t0001g0021a0001c0001t0001g0070a0001c0001t0001g0086others(28): Show | 31 | HG01167.hp2 HG01257.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.125-10387_125-1038 others(8): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874497 | ||||||
chr1:88874633
|
G | A | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-10519C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874633 | ||||||
chr1:88874682
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.125-10568G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874682 | ||||||
chr1:88874695
|
C | T | 15 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0344others(12): Show | 15 | HG00621.hp2 HG01975.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-10581G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874695 | ||||||
chr1:88874761
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.125-10647C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874761 | ||||||
chr1:88874880
|
A | G | 3 | a0001c0001t0001g0344a0001c0001t0002g0343a0001c0001t0002g0346 | 3 | HG02647.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.125-10766T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874880 | ||||||
chr1:88874930
|
T | TAA | 20 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(17): Show | 23 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-10818_125-1081 others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874930 | ||||||
chr1:88874930
|
T | TAAA | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0090others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-10819_125-1081 others(7): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88874930 | ||||||
chr1:88875158
|
C | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0203 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-11044G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875158 | ||||||
chr1:88875316
|
C | G | 1 | a0001c0001t0002g0002 | 4 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-11202G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875316 | ||||||
chr1:88875467
|
A | G | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.125-11353T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875467 | ||||||
chr1:88875661
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.125-11547C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875661 | ||||||
chr1:88875725
|
C | T | 8 | a0001c0001t0002g0188a0001c0001t0003g0182a0001c0001t0003g0183others(5): Show | 8 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+11536G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875725 | ||||||
chr1:88875726
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.124+11535C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875726 | ||||||
chr1:88875823
|
A | G | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+11438T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875823 | ||||||
chr1:88875832
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.124+11429G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875832 | ||||||
chr1:88875837
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124+11424T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875837 | ||||||
chr1:88875888
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+11373G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88875888 | ||||||
chr1:88876005
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0286 | 2 | NA18960.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.124+11256G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876005 | ||||||
chr1:88876033
|
T | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+11228A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876033 | ||||||
chr1:88876075
|
T | TAA | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.124+11185_124+1118 others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876075 | ||||||
chr1:88876153
|
A | G | 35 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(32): Show | 39 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.124+11108T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876153 | ||||||
chr1:88876183
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.124+11078A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876183 | ||||||
chr1:88876270
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124+10991G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876270 | ||||||
chr1:88876386
|
C | A | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+10875G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876386 | ||||||
chr1:88876551
|
T | A | 45 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0086others(42): Show | 49 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.124+10710A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876551 | ||||||
chr1:88876569
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.124+10692G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876569 | ||||||
chr1:88876592
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+10669C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876592 | ||||||
chr1:88876629
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0126 | 2 | NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.124+10632G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876629 | ||||||
chr1:88876661
|
G | A | 15 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0344others(12): Show | 15 | HG00621.hp2 HG01975.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+10600C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876661 | ||||||
chr1:88876758
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.124+10503G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876758 | ||||||
chr1:88876846
|
T | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+10415A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876846 | ||||||
chr1:88876851
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.124+10410G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876851 | ||||||
chr1:88876943
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124+10318A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88876943 | ||||||
chr1:88877282
|
T | G | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+9979A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877282 | ||||||
chr1:88877361
|
A | C | 15 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(12): Show | 18 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.124+9900T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877361 | ||||||
chr1:88877412
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.124+9849T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877412 | ||||||
chr1:88877557
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0203 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+9704G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877557 | ||||||
chr1:88877614
|
C | A | 12 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0090others(9): Show | 12 | HG00621.hp2 HG01975.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.124+9647G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877614 | ||||||
chr1:88877649
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.124+9612G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877649 | ||||||
chr1:88877677
|
A | G | 12 | a0001c0001t0001g0191a0001c0001t0001g0214a0001c0001t0001g0215others(9): Show | 12 | HG00741.hp1 HG01099.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.124+9584T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877677 | ||||||
chr1:88877833
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.124+9428T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877833 | ||||||
chr1:88877924
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0006g0084a0001c0001t0006g0095 | 3 | HG02809.hp1 NA18522.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.124+9337G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877924 | ||||||
chr1:88877925
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124+9336C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88877925 | ||||||
chr1:88878149
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.124+9112T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878149 | ||||||
chr1:88878193
|
G | A | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+9068C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878193 | ||||||
chr1:88878573
|
G | A | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.124+8688C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878573 | ||||||
chr1:88878617
|
C | T | 45 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0086others(42): Show | 49 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.124+8644G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878617 | ||||||
chr1:88878635
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.124+8626C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878635 | ||||||
chr1:88878966
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.124+8295G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878966 | ||||||
chr1:88878995
|
T | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.124+8266A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88878995 | ||||||
chr1:88879203
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124+8058C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879203 | ||||||
chr1:88879246
|
GATAA | G | 8 | a0001c0001t0002g0188a0001c0001t0003g0182a0001c0001t0003g0183others(5): Show | 8 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+8011_124+8014d others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879246 | ||||||
chr1:88879379
|
T | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124+7882A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879379 | ||||||
chr1:88879444
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.124+7817C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879444 | ||||||
chr1:88879583
|
T | TA | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.124+7677dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879583 | ||||||
chr1:88879583
|
TA | T | 28 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0060others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.124+7677delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879583 | ||||||
chr1:88879641
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.124+7620C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879641 | ||||||
chr1:88879675
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124+7586G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879675 | ||||||
chr1:88879827
|
G | A | 32 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(29): Show | 36 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.124+7434C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879827 | ||||||
chr1:88879876
|
T | C | 5 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0219others(2): Show | 5 | HG02071.hp1 HG02165.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+7385A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879876 | ||||||
chr1:88879918
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.124+7343G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88879918 | ||||||
chr1:88880185
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0099others(8): Show | 13 | HG00733.hp1 HG00738.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+7076A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880185 | ||||||
chr1:88880258
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124+7003A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880258 | ||||||
chr1:88880575
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124+6686C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880575 | ||||||
chr1:88880656
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.124+6605A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880656 | ||||||
chr1:88880682
|
A | G | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+6579T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880682 | ||||||
chr1:88880722
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.124+6539A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880722 | ||||||
chr1:88880773
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.124+6488C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880773 | ||||||
chr1:88880844
|
C | A | 45 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0086others(42): Show | 49 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.124+6417G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880844 | ||||||
chr1:88880945
|
G | T | 1 | a0001c0003t0002g0013 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.124+6316C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88880945 | ||||||
chr1:88881007
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124+6254A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881007 | ||||||
chr1:88881008
|
C | CA | 18 | a0001c0001t0001g0048a0001c0001t0001g0073a0001c0001t0001g0077others(15): Show | 19 | HG01192.hp1 HG01952.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.124+6252dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881008 | ||||||
chr1:88881008
|
C | CAA | 22 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(19): Show | 25 | HG00621.hp2 HG01975.hp1 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.124+6251_124+6252d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881008 | ||||||
chr1:88881008
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124+6253G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881008 | ||||||
chr1:88881008
|
CA | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.124+6252delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881008 | ||||||
chr1:88881008
|
CAA | C | 12 | a0001c0001t0001g0081a0001c0001t0001g0131a0001c0001t0001g0134others(9): Show | 12 | HG00738.hp1 HG01109.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.124+6251_124+6252d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881008 | ||||||
chr1:88881009
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124+6252T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881009 | ||||||
chr1:88881030
|
A | C | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG00639.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.124+6231T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881030 | ||||||
chr1:88881051
|
TG | T | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+6209delC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881051 | ||||||
chr1:88881109
|
A | G | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+6152T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881109 | ||||||
chr1:88881169
|
TA | T | 28 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.124+6091delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881169 | ||||||
chr1:88881169
|
TAA | T | 31 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(28): Show | 32 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.124+6090_124+6091d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881169 | ||||||
chr1:88881169
|
TAAA | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+6089_124+6091d others(5): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881169 | ||||||
chr1:88881169
|
TAAAA | T | 9 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(6): Show | 9 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+6088_124+6091d others(6): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881169 | ||||||
chr1:88881265
|
A | G | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+5996T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881265 | ||||||
chr1:88881280
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124+5981A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881280 | ||||||
chr1:88881364
|
C | T | 1 | a0001c0001t0003g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.124+5897G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881364 | ||||||
chr1:88881482
|
T | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+5779A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881482 | ||||||
chr1:88881502
|
A | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.124+5759T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881502 | ||||||
chr1:88881596
|
G | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124+5665C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881596 | ||||||
chr1:88881629
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0153 | 2 | HG01123.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.124+5632G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881629 | ||||||
chr1:88881730
|
CAT | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 7 | HG00408.hp2 HG00423.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+5529_124+5530d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881730 | ||||||
chr1:88881800
|
C | T | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+5461G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88881800 | ||||||
chr1:88882048
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.124+5213C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882048 | ||||||
chr1:88882102
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+5159C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882102 | ||||||
chr1:88882125
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.124+5136G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882125 | ||||||
chr1:88882235
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124+5026G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882235 | ||||||
chr1:88882310
|
C | CA | 84 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0027others(81): Show | 87 | HG00408.hp2 HG00423.hp2 HG01081.hp2 others(84): Show |
intron_variant | MODIFIER | c.124+4950dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
C | CAA | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0209others(4): Show | 7 | HG00741.hp1 HG02622.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+4949_124+4950d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124+4937_124+4950d others(16): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
CA | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(53): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.124+4950delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
CAA | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0085a0001c0001t0001g0086others(16): Show | 20 | HG01167.hp1 HG01169.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.124+4949_124+4950d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
CAAAAAAA | C | 9 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0090others(6): Show | 9 | HG01975.hp1 HG02922.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+4944_124+4950d others(9): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+4940_124+4950d others(13): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882310
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0219a0001c0001t0001g0261 | 2 | HG02165.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.124+4938_124+4950d others(15): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | ||||||
chr1:88882338
|
C | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0237a0001c0001t0001g0238others(11): Show | 15 | HG00323.hp2 HG01081.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.124+4923G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882338 | ||||||
chr1:88882338
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0259 | 3 | HG00639.hp2 HG01175.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.124+4923G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882338 | ||||||
chr1:88882387
|
T | C | 1 | a0001c0002t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124+4874A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882387 | ||||||
chr1:88882404
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.124+4857G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882404 | ||||||
chr1:88882481
|
T | C | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+4780A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882481 | ||||||
chr1:88882556
|
T | TA | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+4704dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882556 | ||||||
chr1:88882854
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+4407T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882854 | ||||||
chr1:88882859
|
A | G | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | HG02132.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.124+4402T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882859 | ||||||
chr1:88882978
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124+4283T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882978 | ||||||
chr1:88883022
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124+4239C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883022 | ||||||
chr1:88883045
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124+4216A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883045 | ||||||
chr1:88883175
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.124+4086G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883175 | ||||||
chr1:88883530
|
G | A | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+3731C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883530 | ||||||
chr1:88883541
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124+3720G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883541 | ||||||
chr1:88883551
|
C | CA | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+3709dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883551 | ||||||
chr1:88883632
|
A | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0260 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.124+3629T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883632 | ||||||
chr1:88883646
|
A | G | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 13 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+3615T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883646 | ||||||
chr1:88883666
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.124+3595T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883666 | ||||||
chr1:88883697
|
G | A | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+3564C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883697 | ||||||
chr1:88883820
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124+3441C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883820 | ||||||
chr1:88883843
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.124+3418A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883843 | ||||||
chr1:88883943
|
G | A | 5 | a0001c0001t0003g0213a0001c0001t0003g0251a0001c0001t0003g0331others(2): Show | 5 | NA18973.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+3318C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88883943 | ||||||
chr1:88884000
|
T | C | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.124+3261A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884000 | ||||||
chr1:88884023
|
C | CT | 18 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0308others(15): Show | 19 | HG00621.hp2 HG01346.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.124+3237dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884023 | ||||||
chr1:88884023
|
C | CTT | 10 | a0001c0001t0001g0344a0001c0001t0002g0090a0001c0001t0002g0119others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+3236_124+3237d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884023 | ||||||
chr1:88884023
|
CT | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.124+3237delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884023 | ||||||
chr1:88884027
|
T | TG | 16 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 16 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.124+3233_124+3234i others(3): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884027 | ||||||
chr1:88884028
|
T | G | 149 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.124+3233A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884028 | ||||||
chr1:88884096
|
C | T | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+3165G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884096 | ||||||
chr1:88884188
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.124+3073G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884188 | ||||||
chr1:88884217
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124+3044C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884217 | ||||||
chr1:88884341
|
G | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+2920C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884341 | ||||||
chr1:88884345
|
A | G | 4 | a0001c0001t0001g0190a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+2916T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884345 | ||||||
chr1:88884370
|
T | C | 2 | a0001c0001t0003g0092a0001c0001t0003g0093 | 2 | NA18966.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.124+2891A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884370 | ||||||
chr1:88884381
|
A | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0260 | 3 | HG01167.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.124+2880T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884381 | ||||||
chr1:88884404
|
C | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG02523.hp1 NA18747.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+2857G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884404 | ||||||
chr1:88884493
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.124+2768T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884493 | ||||||
chr1:88884517
|
C | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18978.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.124+2744G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884517 | ||||||
chr1:88884878
|
A | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0003g0092others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+2383T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884878 | ||||||
chr1:88884934
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.124+2327T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88884934 | ||||||
chr1:88885016
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.124+2245G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885016 | ||||||
chr1:88885058
|
T | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+2203A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885058 | ||||||
chr1:88885226
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0276 | 3 | HG02486.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.124+2035C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885226 | ||||||
chr1:88885256
|
T | C | 2 | a0001c0001t0005g0175a0001c0001t0005g0345 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.124+2005A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885256 | ||||||
chr1:88885273
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.124+1988A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885273 | ||||||
chr1:88885285
|
AAC | A | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+1974_124+1975d others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885285 | ||||||
chr1:88885287
|
C | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.124+1974G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885287 | ||||||
chr1:88885332
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.124+1929G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885332 | ||||||
chr1:88885360
|
A | C | 1 | a0001c0001t0002g0274 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124+1901T>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885360 | ||||||
chr1:88885395
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG01516.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.124+1866C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885395 | ||||||
chr1:88885402
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+1859C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885402 | ||||||
chr1:88885519
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02071.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.124+1742C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885519 | ||||||
chr1:88885577
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0003g0092others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1684C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885577 | ||||||
chr1:88885645
|
G | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124+1616C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885645 | ||||||
chr1:88885674
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+1587G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885674 | ||||||
chr1:88885698
|
C | T | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.124+1563G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885698 | ||||||
chr1:88885761
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0296 | 2 | NA18942.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.124+1500G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885761 | ||||||
chr1:88885822
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124+1439C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885822 | ||||||
chr1:88885878
|
T | C | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+1383A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885878 | ||||||
chr1:88885954
|
C | T | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+1307G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885954 | ||||||
chr1:88885991
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.124+1270C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885991 | ||||||
chr1:88885993
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.124+1268G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88885993 | ||||||
chr1:88886028
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0271 | 2 | NA18977.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.124+1233A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886028 | ||||||
chr1:88886128
|
C | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.124+1133G>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886128 | ||||||
chr1:88886139
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.124+1122C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886139 | ||||||
chr1:88886496
|
AGAT | A | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.124+762_124+764del others(3): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886496 | ||||||
chr1:88886551
|
G | A | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 13 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+710C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886551 | ||||||
chr1:88886615
|
T | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124+646A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886615 | ||||||
chr1:88886712
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+549G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886712 | ||||||
chr1:88886713
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG00323.hp1 HG01255.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.124+548C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886713 | ||||||
chr1:88886812
|
A | AT | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 15 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+448dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886812 | ||||||
chr1:88886814
|
TG | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.124+446delC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886814 | ||||||
chr1:88886815
|
G | T | 45 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0086others(42): Show | 49 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.124+446C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886815 | ||||||
chr1:88886885
|
C | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01496.hp2 HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.124+376G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886885 | ||||||
chr1:88886922
|
TA | T | 10 | a0001c0001t0001g0089a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+338delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886922 | ||||||
chr1:88886923
|
A | T | 18 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(15): Show | 21 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.124+338T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886923 | ||||||
chr1:88886925
|
TA | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0002g0090others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.124+335delT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886925 | ||||||
chr1:88886926
|
A | T | 40 | a0001c0001t0001g0028a0001c0001t0001g0056a0001c0001t0001g0081others(37): Show | 44 | HG00140.hp1 HG00642.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.124+335T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886926 | ||||||
chr1:88886929
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.124+332A>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886929 | ||||||
chr1:88886975
|
G | A | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+286C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886975 | ||||||
chr1:88887004
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.124+257G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88887004 | ||||||
chr1:88887005
|
G | A | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.124+256C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88887005 | ||||||
chr1:88887013
|
G | C | 2 | a0001c0001t0001g0272a0001c0001t0001g0286 | 2 | NA18960.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.124+248C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88887013 | ||||||
chr1:88887449
|
C | T | 1 | a0002c0005t0002g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18-82G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887449 | ||||||
chr1:88887547
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.18-180C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887547 | ||||||
chr1:88887641
|
A | G | 5 | a0001c0001t0002g0274a0001c0001t0002g0336a0001c0001t0002g0337others(2): Show | 5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.18-274T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887641 | ||||||
chr1:88887657
|
T | C | 2 | a0001c0003t0002g0013a0001c0003t0002g0172 | 3 | HG02630.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.18-290A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887657 | ||||||
chr1:88887693
|
G | A | 45 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0086others(42): Show | 49 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.18-326C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887693 | ||||||
chr1:88887861
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.18-494A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887861 | ||||||
chr1:88887952
|
T | G | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.18-585A>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887952 | ||||||
chr1:88887966
|
T | C | 5 | a0001c0001t0003g0213a0001c0001t0003g0251a0001c0001t0003g0331others(2): Show | 5 | NA18973.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.18-599A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88887966 | ||||||
chr1:88888207
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0002t0001g0287 | 3 | HG01192.hp1 HG02083.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.18-840C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888207 | ||||||
chr1:88888255
|
G | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.18-888C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888255 | ||||||
chr1:88888313
|
A | G | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.18-946T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888313 | ||||||
chr1:88888321
|
A | G | 45 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0086others(42): Show | 49 | HG00621.hp2 HG01109.hp1 HG01975.hp1 others(46): Show |
intron_variant | MODIFIER | c.18-954T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888321 | ||||||
chr1:88888360
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.18-993G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888360 | ||||||
chr1:88888428
|
A | G | 5 | a0001c0001t0002g0274a0001c0001t0002g0336a0001c0001t0002g0337others(2): Show | 5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.18-1061T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888428 | ||||||
chr1:88888461
|
T | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.18-1094A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888461 | ||||||
chr1:88888535
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18-1168C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888535 | ||||||
chr1:88888983
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.18-1616G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88888983 | ||||||
chr1:88889016
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.18-1649G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889016 | ||||||
chr1:88889042
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.18-1675G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889042 | ||||||
chr1:88889053
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.18-1686T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889053 | ||||||
chr1:88889076
|
T | C | 1 | a0002c0005t0002g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18-1709A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889076 | ||||||
chr1:88889145
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 6 | HG02486.hp2 HG02886.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-1778C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889145 | ||||||
chr1:88889154
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.18-1787T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889154 | ||||||
chr1:88889178
|
T | C | 1 | a0001c0001t0001g0334 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18-1811A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889178 | ||||||
chr1:88889324
|
G | A | 1 | a0001c0002t0001g0335 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.18-1957C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889324 | ||||||
chr1:88889414
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18-2047G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889414 | ||||||
chr1:88889494
|
T | C | 5 | a0001c0001t0002g0274a0001c0001t0002g0336a0001c0001t0002g0337others(2): Show | 5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.17+1989A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889494 | ||||||
chr1:88889679
|
T | C | 3 | a0001c0001t0001g0344a0001c0001t0002g0343a0001c0001t0002g0346 | 3 | HG02647.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.17+1804A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889679 | ||||||
chr1:88889689
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.17+1794T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889689 | ||||||
chr1:88889697
|
C | T | 3 | a0001c0001t0001g0344a0001c0001t0002g0343a0001c0001t0002g0346 | 3 | HG02647.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.17+1786G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889697 | ||||||
chr1:88889718
|
G | A | 10 | a0001c0001t0001g0081a0001c0001t0002g0188a0001c0001t0003g0171others(7): Show | 10 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.17+1765C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889718 | ||||||
chr1:88889726
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.17+1757A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889726 | ||||||
chr1:88889757
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17+1726C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889757 | ||||||
chr1:88889907
|
G | C | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0003g0092others(8): Show | 11 | HG00621.hp2 HG01975.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.17+1576C>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889907 | ||||||
chr1:88889912
|
T | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(30): Show | 37 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.17+1571A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889912 | ||||||
chr1:88889963
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.17+1520A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88889963 | ||||||
chr1:88890014
|
C | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 13 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.17+1469G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890014 | ||||||
chr1:88890157
|
T | TAA | 27 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(24): Show | 27 | HG00621.hp2 HG01975.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.17+1324_17+1325dup others(2): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890157 | ||||||
chr1:88890157
|
T | TAAAA | 3 | a0001c0001t0002g0002a0001c0001t0002g0347a0001c0001t0002g0348 | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+1322_17+1325dup others(4): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890157 | ||||||
chr1:88890281
|
C | G | 2 | a0001c0001t0006g0084a0001c0001t0006g0095 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.17+1202G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890281 | ||||||
chr1:88890406
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.17+1077G>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890406 | ||||||
chr1:88890501
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | NA18994.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.17+982G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890501 | ||||||
chr1:88890710
|
T | C | 2 | a0001c0001t0003g0092a0001c0001t0003g0093 | 2 | NA18966.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.17+773A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890710 | ||||||
chr1:88890853
|
G | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | NA18990.hp1 NA18991.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+630C>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890853 | ||||||
chr1:88890909
|
A | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.17+574T>A | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88890909 | ||||||
chr1:88891120
|
C | CG | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(69): Show | 74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.17+362dupC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891120 | ||||||
chr1:88891120
|
C | CGG | 62 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0027others(59): Show | 63 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.17+361_17+362dupCC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891120 | ||||||
chr1:88891120
|
C | CGGG | 54 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(51): Show | 55 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.17+360_17+362dupCC others(1): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891120 | ||||||
chr1:88891120
|
C | CGGGG | 25 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(22): Show | 25 | HG00438.hp2 HG01257.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.17+359_17+362dupCC others(2): Show |
GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891120 | ||||||
chr1:88891151
|
G | A | 8 | a0001c0001t0002g0188a0001c0001t0003g0182a0001c0001t0003g0183others(5): Show | 8 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+332C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891151 | ||||||
chr1:88891161
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.17+322T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891161 | ||||||
chr1:88891179
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.17+304T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891179 | ||||||
chr1:88891218
|
G | A | 2 | a0001c0001t0001g0340a0001c0001t0007g0341 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.17+265C>T | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891218 | ||||||
chr1:88891245
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.17+238T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891245 | ||||||
chr1:88891321
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17+162A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891321 | ||||||
chr1:88891371
|
C | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01496.hp2 HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.17+112G>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891371 | ||||||
chr1:88891385
|
T | C | 7 | a0001c0001t0001g0344a0001c0001t0002g0002a0001c0001t0002g0343others(4): Show | 10 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+98A>G | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891385 | ||||||
chr1:88891475
|
A | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG03041.hp2 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.17+8T>C | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 1/6 | chr1 | 88891475 |