Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 316 | 371 | 96 | 68 | 156 | 12 | 37 | 120 | GTF2B_chr1_88847633_88896567 | GTF2B | MASTS others(311): Show |
chr1 | 88847633 | 88896567 |
| a0002 | 0/0 | 316 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | MASTS others(311): Show |
chr1 | 88847633 | 88896567 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 948 | 355 | 83 | 68 | 154 | 12 | 37 | GTF2B_chr1_88847633_88896567 | GTF2B | ATGGC others(943): Show |
chr1 | 88847633 | 88896567 | ||
| a0001c0002 | 1/0 | 948 | 11 | 10 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | ATGGC others(943): Show |
chr1 | 88847633 | 88896567 | ||
| a0001c0003 | 0/0 | 948 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | ATGGC others(943): Show |
chr1 | 88847633 | 88896567 | ||
| a0001c0004 | 0/0 | 948 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | ATGGC others(943): Show |
chr1 | 88847633 | 88896567 | ||
| a0002c0005 | 0/0 | 948 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | ATGGC others(943): Show |
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 | GCCAC others(1594): Show |
chr1 | 88847633 | 88896567 |
| a0001c0001t0002 | 0/0 | 1606 | 23 | 20 | 3 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1601): Show |
chr1 | 88847633 | 88896567 |
| a0001c0001t0003 | 0/0 | 1606 | 22 | 7 | 2 | 12 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1601): Show |
chr1 | 88847633 | 88896567 |
| a0001c0001t0004 | 0/0 | 1599 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1594): Show |
chr1 | 88847633 | 88896567 |
| a0001c0001t0005 | 0/0 | 1606 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1601): Show |
chr1 | 88847633 | 88896567 |
| a0001c0001t0006 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1597): Show |
chr1 | 88847633 | 88896567 |
| a0001c0001t0007 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1594): Show |
chr1 | 88847633 | 88896567 |
| a0001c0002t0001 | 1/0 | 1599 | 11 | 10 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1594): Show |
chr1 | 88847633 | 88896567 |
| a0001c0003t0002 | 0/0 | 1606 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1601): Show |
chr1 | 88847633 | 88896567 |
| a0001c0004t0003 | 0/0 | 1606 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1601): Show |
chr1 | 88847633 | 88896567 |
| a0002c0005t0002 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | GCCAC others(1601): Show |
chr1 | 88847633 | 88896567 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 2 | 8 | 1 | 2 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0130 | 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 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0274 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0001g0322 | 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 |
| a0001c0001t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0003t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0001c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| a0002c0005t0002g0113 | 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 | g0137 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | CHS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0160 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | ESN | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03688 | hp1 | a0002 | c0005 | t0002 | g0113 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0065 | 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 | g0109 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | 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 | g0010 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0101 | 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 | g0048 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | 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 | g0238 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19064 | hp2 | a0001 | c0004 | t0003 | g0165 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19082 | hp1 | a0001 | c0004 | t0003 | g0164 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0307 | 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 | g0208 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | ASW | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0311 | EUR | TSI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | GIH | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0325 | AFR | MSL | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0231 | REF | REF | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0295 | REF | REF | GTF2B_chr1_88847633_88896567 | GTF2B | chr1 | 88847633 | 88896567 |
| view | 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 |
| view | 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 | a0001c0001 a0001c0003 a0001c0004 others(1): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): 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 |
| view | 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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(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 | a0001c0001t0003 a0001c0004t0003 |
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 | a0001c0001t0002 a0001c0001t0005 a0001c0003t0002 others(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 |
| view | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0143 |
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 | a0001c0001t0002g0326 | 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 | a0001c0001t0003g0159 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0297 |
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 | a0001c0001t0003g0070 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0186 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0022 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0297 |
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 | a0001c0002t0001g0264 a0001c0002t0001g0292 |
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 | a0001c0001t0002g0258 a0001c0001t0002g0318 a0001c0001t0002g0319 |
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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0003g0070 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0183 | 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 | 25 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0020 others(22): 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 | a0001c0001t0003g0070 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0156 a0001c0001t0003g0131 a0001c0004t0003g0165 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0002g0114 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0155 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0256 a0001c0001t0002g0021 others(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 | a0001c0001t0001g0239 | 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 | a0001c0001t0003g0159 | 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 | a0001c0001t0002g0316 a0001c0001t0002g0317 |
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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0080 a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0106 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0070 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0003g0201 a0001c0001t0003g0238 a0001c0001t0003g0311 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0003g0159 a0001c0001t0003g0170 a0001c0001t0003g0171 others(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 | a0001c0001t0002g0176 a0001c0001t0002g0323 a0001c0001t0002g0326 |
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 | a0001c0001t0002g0176 a0001c0001t0002g0323 a0001c0001t0002g0326 |
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 | a0001c0001t0004g0293 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | 71 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0302 a0001c0001t0001g0304 |
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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0089 a0001c0001t0003g0070 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0112 a0001c0001t0002g0176 a0001c0001t0002g0212 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0089 others(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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(47): 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(230): 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 | a0001c0001t0001g0202 a0001c0001t0001g0245 |
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 | 11 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0060 others(8): 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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.817+761dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856444 | |||||||
| chr1:88856496 | A | C | 1 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0211 | 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 | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(158): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.817+401dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 6/6 | chr1 | 88856804 | |||||||
| chr1:88856804 | G | GTT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0021 others(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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0003g0201 a0001c0001t0003g0312 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0133 a0001c0001t0001g0213 others(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 |
244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): 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 | a0001c0001t0001g0031 a0001c0001t0001g0046 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0314 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0081 a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0005g0163 others(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 | a0001c0001t0002g0162 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0002g0319 | 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 | a0001c0001t0002g0319 | 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 | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(154): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0176 others(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 | a0001c0001t0002g0319 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0119 others(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 | a0001c0001t0007g0321 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0059 a0001c0001t0001g0061 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0003g0201 | 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 | a0001c0001t0003g0312 | 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 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0176 others(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 | a0001c0001t0002g0258 | 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 | a0001c0001t0001g0100 a0001c0001t0002g0114 a0001c0001t0002g0115 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0176 others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0002g0176 a0001c0001t0003g0159 a0001c0001t0003g0170 others(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 | a0001c0001t0003g0170 a0001c0001t0003g0173 a0001c0001t0003g0174 |
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 | a0001c0001t0005g0163 a0001c0001t0005g0325 |
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 | a0001c0001t0001g0111 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0112 a0001c0001t0002g0212 a0002c0005t0002g0113 |
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 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0088 others(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 | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(280): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0007g0321 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0176 others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 |
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 | a0001c0001t0003g0201 a0001c0001t0003g0238 a0001c0001t0003g0311 others(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 | a0001c0001t0003g0201 a0001c0001t0003g0238 a0001c0001t0003g0311 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0176 others(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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0043 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0001t0001g0195 others(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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0302 a0001c0001t0001g0304 |
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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0176 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0129 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0001t0001g0195 others(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 | a0001c0001t0002g0162 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0003g0090 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0088 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0112 a0001c0001t0002g0212 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0320 a0001c0001t0007g0321 |
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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0207 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0135 |
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 | a0001c0001t0001g0236 | 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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(72): 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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0285 | 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 | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(154): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0004g0293 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0003t0002g0019 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0062 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0003 others(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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0241 | 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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0136 | 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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(72): 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 | a0001c0001t0003g0201 a0001c0001t0003g0238 a0001c0001t0003g0311 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0314 | 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 | a0001c0001t0001g0230 a0001c0001t0001g0257 |
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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0125 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(299): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.125-4627delA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88868740 | |||||||
| chr1:88868845 | A | C | 47 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0263 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0004g0293 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0273 a0001c0001t0002g0003 a0001c0001t0002g0021 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0005g0163 a0001c0001t0005g0325 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0155 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | 13 | a0001c0001t0001g0028 a0001c0001t0001g0049 a0001c0001t0001g0056 others(10): Show |
13 | HG00733.hp1 HG01109.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-6783dupA | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88870896 | |||||||
| chr1:88870896 | CT | C | 39 | a0001c0001t0001g0018 a0001c0001t0001g0079 a0001c0001t0001g0081 others(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 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0114 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0002g0088 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): 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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): 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 | a0001c0001t0003g0201 a0001c0001t0003g0312 a0001c0001t0003g0313 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(153): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(129): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.125-8342dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88872455 | |||||||
| chr1:88872455 | T | TAA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(74): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0099 others(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 | 47 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0259 others(44): 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | 53 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0027 others(50): 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0079 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0112 a0001c0001t0002g0327 others(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 | a0001c0001t0002g0176 a0001c0001t0003g0171 |
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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0150 | 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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0078 | 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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | a0001c0001t0003g0166 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0002g0316 a0001c0001t0002g0317 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0002g0326 a0001c0003t0002g0019 a0001c0004t0003g0164 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0088 others(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 | 17 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(14): 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 | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): 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 | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): 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 | a0001c0001t0001g0024 a0001c0001t0001g0064 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0324 others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0324 a0001c0001t0002g0323 a0001c0001t0002g0326 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
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 | a0001c0001t0002g0003 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0002g0176 a0001c0001t0003g0170 a0001c0001t0003g0171 others(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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(75): 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0324 others(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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0179 a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(154): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(65): 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 | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(66): 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0002g0176 a0001c0001t0003g0170 a0001c0001t0003g0171 others(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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0026 | 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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): 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 | 26 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0047 others(23): 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 | a0001c0001t0003g0159 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0271 | 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 | 10 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0097 others(7): 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0050 | 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 | a0001c0001t0002g0162 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0003t0002g0019 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0071 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0252 | 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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(108): 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 | a0001c0001t0001g0079 a0001c0001t0001g0126 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0252 | 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 | a0001c0001t0002g0318 a0001c0001t0002g0319 |
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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0003g0168 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0142 |
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 | 4 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0290 others(1): 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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0127 | 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 | 77 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(74): Show |
86 | HG00408.hp2 HG00423.hp2 HG01081.hp2 others(83): Show |
intron_variant | MODIFIER | c.124+4950dupT | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88882310 | |||||||
| chr1:88882310 | C | CAA | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0112 | 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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): 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 | a0001c0001t0001g0018 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0088 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0207 a0001c0001t0001g0246 |
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 | 11 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0224 others(8): 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 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0244 |
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 | a0001c0002t0001g0298 | 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 | a0001c0001t0003g0159 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0230 | 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 | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(313): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): 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 | a0001c0001t0003g0201 a0001c0001t0003g0238 a0001c0001t0003g0311 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0324 a0001c0001t0002g0088 a0001c0001t0002g0114 others(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 | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(73): 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 | 15 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0051 others(12): 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 | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(139): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0277 a0001c0001t0001g0278 others(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 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0263 |
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 | a0001c0001t0005g0163 a0001c0001t0005g0325 |
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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0003g0090 others(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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0054 | 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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0179 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0162 others(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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0255 |
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 | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(153): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): 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 | a0001c0001t0002g0176 | 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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(148): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.124+446delC | GTF2B | ENSG00000137947.12 | transcript | ENST00000370500.10 | protein_coding | 2/6 | chr1 | 88886814 | |||||||
| chr1:88886815 | G | T | 45 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0001g0084 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0079 others(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 | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(76): 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0053 | 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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0268 |
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 | a0002c0005t0002g0113 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0002g0258 a0001c0001t0002g0316 a0001c0001t0002g0317 others(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 | a0001c0003t0002g0019 a0001c0003t0002g0160 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0003g0201 a0001c0001t0003g0238 a0001c0001t0003g0311 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0118 a0001c0002t0001g0269 |
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 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0118 | 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 | a0001c0001t0002g0258 a0001c0001t0002g0316 a0001c0001t0002g0317 others(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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0324 | 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 | a0001c0001t0001g0259 a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0273 | 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 | a0002c0005t0002g0113 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0155 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0314 | 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 | a0001c0002t0001g0315 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0258 a0001c0001t0002g0316 a0001c0001t0002g0317 others(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 | a0001c0001t0001g0324 a0001c0001t0002g0323 a0001c0001t0002g0326 |
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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0324 a0001c0001t0002g0323 a0001c0001t0002g0326 |
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 | a0001c0001t0001g0079 a0001c0001t0002g0176 a0001c0001t0003g0159 others(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 | a0001c0001t0002g0088 | 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 | a0001c0001t0003g0159 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0327 a0001c0001t0002g0328 |
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 | a0001c0001t0006g0082 a0001c0001t0006g0093 |
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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0116 |
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 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | 69 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(66): 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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(53): 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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(49): Show |
54 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(51): 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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0002g0176 a0001c0001t0003g0170 a0001c0001t0003g0171 others(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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(116): 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 | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(56): 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 | a0001c0001t0001g0320 a0001c0001t0007g0321 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0322 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0001g0324 a0001c0001t0002g0003 a0001c0001t0002g0323 others(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 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
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 |