Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2965 |
| ensemblid | ENSG00000110768.12 |
| hgncid | 4655 |
| symbol | GTF2H1 |
| name | general transcription factor IIH subunit 1 |
| refseq_nuc | NM_005316.4 |
| refseq_prot | NP_005307.1 |
| ensembl_nuc | ENST00000265963.9 |
| ensembl_prot | ENSP00000265963.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 18322567 |
| end | 18367045 |
| strand | + |
| ver | v1.2 |
| region | chr11:18322567-18367045 |
| region5000 | chr11:18317567-18372045 |
| regionname0 | GTF2H1_chr11_18322567_18367045 |
| regionname5000 | GTF2H1_chr11_18317567_18372045 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 548 | 365 | 98 | 66 | 154 | 16 | 29 | 118 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | MATSS others(543): Show |
chr11 | 18317567 | 18372045 |
| a0002 | 0/0 | 548 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | MATSS others(543): Show |
chr11 | 18317567 | 18372045 |
| a0003 | 0/0 | 548 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | MATSS others(543): Show |
chr11 | 18317567 | 18372045 |
| a0004 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | MATSS others(543): Show |
chr11 | 18317567 | 18372045 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1644 | 360 | 98 | 63 | 152 | 16 | 29 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | ATGGC others(1639): Show |
chr11 | 18317567 | 18372045 | ||
| a0001c0002 | 0/0 | 1644 | 4 | 0 | 2 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | ATGGC others(1639): Show |
chr11 | 18317567 | 18372045 | ||
| a0001c0004 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | ATGGC others(1639): Show |
chr11 | 18317567 | 18372045 | ||
| a0002c0003 | 0/0 | 1644 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | ATGGC others(1639): Show |
chr11 | 18317567 | 18372045 | ||
| a0003c0006 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | ATGGC others(1639): Show |
chr11 | 18317567 | 18372045 | ||
| a0004c0005 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | ATGGC others(1639): Show |
chr11 | 18317567 | 18372045 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3012 | 197 | 68 | 31 | 72 | 5 | 19 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0002 | 0/0 | 3013 | 119 | 5 | 22 | 72 | 10 | 10 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0003 | 0/0 | 3012 | 16 | 15 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0004 | 0/0 | 3013 | 8 | 8 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0005 | 0/0 | 3013 | 7 | 0 | 6 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0006 | 0/0 | 3012 | 4 | 0 | 0 | 4 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0007 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0008 | 0/0 | 3013 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0009 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0010 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0011 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0012 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0013 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0001t0014 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0002t0001 | 0/0 | 3012 | 3 | 0 | 1 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0001c0002t0004 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0001c0004t0002 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0002c0003t0002 | 0/0 | 3013 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| a0002c0003t0007 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0003c0006t0001 | 0/0 | 3012 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3007): Show |
chr11 | 18317567 | 18372045 |
| a0004c0005t0002 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | AGACT others(3008): Show |
chr11 | 18317567 | 18372045 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 0 | 3 | 13 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 1 | 2 | 3 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0005g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0011g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0002t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0001c0004t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0002c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0002c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0002c0003t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0003c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| a0004c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | GBR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | GBR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | FIN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0098 | EUR | FIN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0159 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01106 | hp2 | a0001 | c0004 | t0002 | g0113 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0104 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0160 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | IBS | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01934 | hp2 | a0001 | c0002 | t0004 | g0220 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02148 | hp2 | a0001 | c0001 | t0011 | g0209 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CDX | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CDX | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0053 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03834 | hp1 | a0003 | c0006 | t0001 | g0165 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | STU | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18942 | hp1 | a0002 | c0003 | t0002 | g0153 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18942 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18946 | hp2 | a0002 | c0003 | t0002 | g0157 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18948 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0099 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18983 | hp1 | a0004 | c0005 | t0002 | g0156 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | LWK | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | LWK | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19059 | hp1 | a0002 | c0003 | t0007 | g0152 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ASW | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ASW | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | GIH | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0190 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | USA | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | USA | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | USA | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | USA | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0245 | REF | REF | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | GTF2H1_chr11_18317567_18372045 | GTF2H1 | chr11 | 18317567 | 18372045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18341353 | C | T | 1 | a0002 | 3 | NA18942.hp1 NA18946.hp2 NA19059.hp1 |
missense_variant | MODERATE | c.700C>T | p.Arg234Trp | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 6/15 | 889/3012 | 700/1647 | 234/548 | chr11 | 18341353 | |||
| chr11:18341530 | C | G | 1 | a0003 | 1 | HG03834.hp1 | missense_variant&splice_region_variant | MODERATE | c.760C>G | p.Leu254Val | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/15 | 949/3012 | 760/1647 | 254/548 | chr11 | 18341530 | |||
| chr11:18365850 | G | A | 1 | a0004 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.1628G>A | p.Arg543His | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 1817/3012 | 1628/1647 | 543/548 | chr11 | 18365850 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18335872 | A | G | 1 | a0001c0002 | 4 | HG01934.hp2 HG01981.hp1 NA18962.hp2 others(1): Show |
synonymous_variant | LOW | c.273A>G | p.Ala91Ala | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/15 | 462/3012 | 273/1647 | 91/548 | chr11 | 18335872 | |||
| chr11:18341548 | T | C | 1 | a0001c0004 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.778T>C | p.Leu260Leu | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/15 | 967/3012 | 778/1647 | 260/548 | chr11 | 18341548 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18322714 | C | A | 1 | a0001c0001t0009 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/15 | 10361 | chr11 | 18322714 | ||||||
| chr11:18365926 | C | T | 1 | a0001c0001t0014 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 57 | chr11 | 18365926 | ||||||
| chr11:18366015 | A | G | 1 | a0001c0001t0013 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 146 | chr11 | 18366015 | ||||||
| chr11:18366118 | C | T | 1 | a0001c0001t0003 | 16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 249 | chr11 | 18366118 | ||||||
| chr11:18366575 | A | C | 1 | a0001c0001t0006 | 4 | NA18955.hp2 NA18956.hp2 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 706 | chr11 | 18366575 | ||||||
| chr11:18366581 | G | C | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(7): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*712G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 712 | chr11 | 18366581 | ||||||
| chr11:18366764 | A | T | 2 | a0001c0001t0008 a0001c0001t0012 |
3 | HG01167.hp1 HG01169.hp1 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*895A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 895 | chr11 | 18366764 | ||||||
| chr11:18366828 | A | G | 1 | a0001c0001t0012 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 959 | chr11 | 18366828 | ||||||
| chr11:18366859 | G | A | 1 | a0001c0001t0010 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*990G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 990 | chr11 | 18366859 | ||||||
| chr11:18366894 | C | CA | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(7): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1041dupA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 1042 | INFO_REALIGN_3_PRIME | chr11 | 18366894 | |||||
| chr11:18366894 | C | T | 1 | a0001c0001t0011 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1025C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 1025 | chr11 | 18366894 | ||||||
| chr11:18366917 | C | G | 1 | a0001c0001t0005 | 7 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1048C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 15/15 | 1048 | chr11 | 18366917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18322804 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0031 |
4 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+64G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18322804 | |||||||
| chr11:18322929 | A | G | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+189A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18322929 | |||||||
| chr11:18323068 | G | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+328G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323068 | |||||||
| chr11:18323074 | T | G | 1 | a0001c0001t0002g0038 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-16+334T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323074 | |||||||
| chr11:18323081 | G | C | 4 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG00558.hp1 HG02074.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+341G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323081 | |||||||
| chr11:18323173 | T | A | 1 | a0001c0001t0001g0043 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-16+433T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323173 | |||||||
| chr11:18323303 | A | AT | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+572dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18323303 | ||||||
| chr11:18323558 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+818C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323558 | |||||||
| chr11:18323563 | A | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+823A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323563 | |||||||
| chr11:18323564 | C | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+824C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323564 | |||||||
| chr11:18323570 | A | C | 8 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(5): Show |
8 | HG02451.hp1 HG02738.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+830A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323570 | |||||||
| chr11:18323720 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-16+980A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323720 | |||||||
| chr11:18323800 | CACAGTTT others(4): Show |
C | 26 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
27 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.-16+1063_-16+1073d others(13): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18323800 | ||||||
| chr11:18323827 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-16+1087T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18323827 | |||||||
| chr11:18324052 | AT | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-16+1327delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18324052 | ||||||
| chr11:18324069 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG01074.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-16+1329A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324069 | |||||||
| chr11:18324143 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-16+1403C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324143 | |||||||
| chr11:18324226 | T | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+1486T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324226 | |||||||
| chr11:18324282 | C | T | 6 | a0001c0001t0002g0026 a0001c0001t0002g0038 a0001c0001t0002g0205 others(3): Show |
7 | HG00609.hp1 NA18951.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+1542C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324282 | |||||||
| chr11:18324301 | G | A | 1 | a0001c0001t0011g0209 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-16+1561G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324301 | |||||||
| chr11:18324418 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+1678G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324418 | |||||||
| chr11:18324467 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | NA18965.hp2 NA18972.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+1727T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324467 | |||||||
| chr11:18324469 | G | A | 1 | a0001c0001t0004g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16+1729G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324469 | |||||||
| chr11:18324515 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG01256.hp1 HG01258.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-16+1775C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324515 | |||||||
| chr11:18324705 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1965C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18324705 | |||||||
| chr11:18324722 | CTAGTAGT others(6): Show |
C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-16+1984_-16+1996d others(15): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18324722 | ||||||
| chr11:18325000 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-16+2260C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325000 | |||||||
| chr11:18325136 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+2396T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325136 | |||||||
| chr11:18325252 | A | G | 4 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2512A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325252 | |||||||
| chr11:18325348 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-16+2608A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325348 | |||||||
| chr11:18325365 | G | A | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+2625G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325365 | |||||||
| chr11:18325537 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+2797C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325537 | |||||||
| chr11:18325678 | G | GA | 9 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
12 | HG01891.hp1 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-16+2948dupA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18325678 | ||||||
| chr11:18325726 | A | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-16+2986A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325726 | |||||||
| chr11:18325854 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-16+3114A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325854 | |||||||
| chr11:18325989 | C | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
60 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-16+3249C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18325989 | |||||||
| chr11:18326003 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-16+3263A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326003 | |||||||
| chr11:18326247 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-16+3507C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326247 | |||||||
| chr11:18326447 | G | C | 105 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(102): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-16+3707G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326447 | |||||||
| chr11:18326521 | C | CA | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-16+3792dupA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18326521 | ||||||
| chr11:18326609 | C | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+3869C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326609 | |||||||
| chr11:18326639 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+3899C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326639 | |||||||
| chr11:18326718 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-16+3978C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326718 | |||||||
| chr11:18326726 | C | G | 1 | a0001c0001t0002g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-16+3986C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326726 | |||||||
| chr11:18326760 | T | G | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+4020T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326760 | |||||||
| chr11:18326821 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-16+4081G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326821 | |||||||
| chr11:18326868 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-16+4128A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326868 | |||||||
| chr11:18326922 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-16+4182G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326922 | |||||||
| chr11:18326923 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-16+4183T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326923 | |||||||
| chr11:18326976 | T | C | 1 | a0001c0001t0002g0086 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-16+4236T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18326976 | |||||||
| chr11:18326994 | TA | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+4264delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18326994 | ||||||
| chr11:18327029 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-16+4289G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327029 | |||||||
| chr11:18327034 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-16+4294T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327034 | |||||||
| chr11:18327115 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-16+4375G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327115 | |||||||
| chr11:18327492 | C | G | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+4752C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327492 | |||||||
| chr11:18327564 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16+4824A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327564 | |||||||
| chr11:18327730 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+4990A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327730 | |||||||
| chr11:18327931 | G | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15-5129G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327931 | |||||||
| chr11:18327933 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-15-5127G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18327933 | |||||||
| chr11:18328202 | CA | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(176): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-15-4840delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18328202 | ||||||
| chr11:18328202 | CAA | C | 14 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0002g0155 others(11): Show |
19 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15-4841_-15-4840d others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18328202 | ||||||
| chr11:18328235 | G | A | 3 | a0001c0001t0004g0216 a0001c0001t0004g0217 a0001c0001t0004g0218 |
3 | HG02818.hp2 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-15-4825G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18328235 | |||||||
| chr11:18328356 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0031 |
3 | HG01243.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-15-4704A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18328356 | |||||||
| chr11:18328512 | C | CA | 11 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0161 others(8): Show |
12 | HG00621.hp1 HG01074.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-4531dupA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18328512 | ||||||
| chr11:18328512 | CA | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
9 | HG02602.hp2 HG03491.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-4531delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18328512 | ||||||
| chr11:18328529 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15-4531A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18328529 | |||||||
| chr11:18328530 | T | A | 4 | a0001c0002t0001g0221 a0001c0002t0001g0222 a0001c0002t0001g0250 others(1): Show |
4 | HG01934.hp2 HG01981.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-4530T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18328530 | |||||||
| chr11:18328615 | A | G | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-4445A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18328615 | |||||||
| chr11:18329017 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-15-4043T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18329017 | |||||||
| chr11:18329176 | C | CATT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-15-3882_-15-3881i others(5): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18329176 | ||||||
| chr11:18329237 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-15-3823C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18329237 | |||||||
| chr11:18329351 | C | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(202): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-15-3709C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18329351 | |||||||
| chr11:18329541 | C | T | 3 | a0002c0003t0002g0153 a0002c0003t0002g0157 a0002c0003t0007g0152 |
3 | NA18942.hp1 NA18946.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.-15-3519C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18329541 | |||||||
| chr11:18329841 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-15-3219A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18329841 | |||||||
| chr11:18329974 | C | G | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-3086C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18329974 | |||||||
| chr11:18330045 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0210 |
2 | NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-15-3015G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18330045 | |||||||
| chr11:18330414 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15-2646C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18330414 | |||||||
| chr11:18330586 | C | T | 1 | a0004c0005t0002g0156 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-15-2474C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18330586 | |||||||
| chr11:18330606 | G | T | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-15-2454G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18330606 | |||||||
| chr11:18330659 | C | T | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-2401C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18330659 | |||||||
| chr11:18330886 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(108): Show |
152 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-15-2174G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18330886 | |||||||
| chr11:18331027 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-15-2033A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331027 | |||||||
| chr11:18331138 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(143): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-15-1922C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331138 | |||||||
| chr11:18331143 | G | C | 1 | a0001c0001t0004g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-15-1917G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331143 | |||||||
| chr11:18331191 | G | C | 1 | a0001c0001t0001g0059 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-15-1869G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331191 | |||||||
| chr11:18331218 | G | C | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15-1842G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331218 | |||||||
| chr11:18331434 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
6 | HG00423.hp2 HG01255.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-1626A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331434 | |||||||
| chr11:18331437 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-1623C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331437 | |||||||
| chr11:18331476 | G | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-1584G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331476 | |||||||
| chr11:18331481 | A | C | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01070.hp2 HG01433.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-1579A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331481 | |||||||
| chr11:18331527 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15-1533G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331527 | |||||||
| chr11:18331705 | G | T | 2 | a0001c0001t0001g0182 a0001c0001t0004g0212 |
2 | HG02145.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-15-1355G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331705 | |||||||
| chr11:18331758 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-15-1302C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331758 | |||||||
| chr11:18331892 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-15-1168C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18331892 | |||||||
| chr11:18332093 | CG | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-15-961delG | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 18332093 | ||||||
| chr11:18332151 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-15-909A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332151 | |||||||
| chr11:18332196 | G | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-864G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332196 | |||||||
| chr11:18332354 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15-706A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332354 | |||||||
| chr11:18332372 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-15-688C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332372 | |||||||
| chr11:18332396 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-15-664A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332396 | |||||||
| chr11:18332525 | A | G | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15-535A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332525 | |||||||
| chr11:18332795 | G | A | 1 | a0001c0001t0014g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-15-265G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332795 | |||||||
| chr11:18332808 | T | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0015 others(12): Show |
19 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-252T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332808 | |||||||
| chr11:18332850 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15-210C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332850 | |||||||
| chr11:18332895 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-15-165G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332895 | |||||||
| chr11:18332981 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-15-79G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332981 | |||||||
| chr11:18332984 | A | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0146 a0001c0001t0002g0147 others(1): Show |
4 | HG00621.hp1 HG00642.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-76A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 1/14 | chr11 | 18332984 | |||||||
| chr11:18333255 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.154+27G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333255 | |||||||
| chr11:18333330 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.154+102T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333330 | |||||||
| chr11:18333416 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.154+188G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333416 | |||||||
| chr11:18333448 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.154+220A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333448 | |||||||
| chr11:18333555 | T | G | 12 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0087 others(9): Show |
19 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.154+327T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333555 | |||||||
| chr11:18333761 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.154+533G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333761 | |||||||
| chr11:18333892 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+664C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333892 | |||||||
| chr11:18333902 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG03704.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.154+674G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18333902 | |||||||
| chr11:18334052 | C | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.154+824C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334052 | |||||||
| chr11:18334080 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.154+852A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334080 | |||||||
| chr11:18334273 | G | A | 2 | a0001c0001t0002g0154 a0001c0001t0009g0099 |
2 | NA18946.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.154+1045G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334273 | |||||||
| chr11:18334349 | C | T | 3 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG00140.hp1 HG00639.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.154+1121C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334349 | |||||||
| chr11:18334360 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.154+1132C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334360 | |||||||
| chr11:18334748 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
2 | NA18968.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.155-1006A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334748 | |||||||
| chr11:18334793 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-961A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334793 | |||||||
| chr11:18334843 | A | G | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-911A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334843 | |||||||
| chr11:18334887 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.155-867A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334887 | |||||||
| chr11:18334919 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.155-835C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334919 | |||||||
| chr11:18334922 | T | A | 1 | a0001c0001t0004g0216 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.155-832T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334922 | |||||||
| chr11:18334987 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.155-767A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18334987 | |||||||
| chr11:18335084 | G | T | 1 | a0001c0001t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.155-670G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335084 | |||||||
| chr11:18335117 | A | G | 1 | a0001c0001t0005g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.155-637A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335117 | |||||||
| chr11:18335218 | C | G | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.155-536C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335218 | |||||||
| chr11:18335567 | G | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-187G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335567 | |||||||
| chr11:18335633 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.155-121A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335633 | |||||||
| chr11:18335651 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.155-103A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335651 | |||||||
| chr11:18335658 | A | G | 1 | a0001c0001t0004g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.155-96A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335658 | |||||||
| chr11:18335723 | A | G | 106 | a0001c0001t0001g0180 a0001c0001t0002g0002 a0001c0001t0002g0003 others(103): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.155-31A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 2/14 | chr11 | 18335723 | |||||||
| chr11:18336034 | T | A | 1 | a0001c0001t0003g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.347+88T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336034 | |||||||
| chr11:18336077 | TTTTTG | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0024 others(31): Show |
45 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.347+140_347+144del others(5): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 18336077 | ||||||
| chr11:18336083 | TTTTG | T | 28 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(25): Show |
30 | HG01070.hp2 HG01433.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.347+153_347+156del others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 18336083 | ||||||
| chr11:18336419 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347+473C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336419 | |||||||
| chr11:18336566 | C | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+620C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336566 | |||||||
| chr11:18336696 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+750T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336696 | |||||||
| chr11:18336757 | A | AT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(154): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.347+826dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 18336757 | ||||||
| chr11:18336796 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.347+850C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336796 | |||||||
| chr11:18336907 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.347+961A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336907 | |||||||
| chr11:18336908 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.347+962C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336908 | |||||||
| chr11:18336921 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.347+975A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336921 | |||||||
| chr11:18336970 | C | G | 1 | a0001c0001t0003g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.347+1024C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336970 | |||||||
| chr11:18336998 | G | T | 1 | a0001c0001t0002g0193 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.347+1052G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18336998 | |||||||
| chr11:18337023 | T | G | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.347+1077T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337023 | |||||||
| chr11:18337061 | T | A | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.348-1048T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337061 | |||||||
| chr11:18337236 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348-873C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337236 | |||||||
| chr11:18337314 | C | T | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-795C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337314 | |||||||
| chr11:18337316 | C | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
60 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.348-793C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337316 | |||||||
| chr11:18337330 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.348-779A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337330 | |||||||
| chr11:18337408 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.348-701G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337408 | |||||||
| chr11:18337557 | C | A | 3 | a0001c0001t0004g0216 a0001c0001t0004g0217 a0001c0001t0004g0218 |
3 | HG02818.hp2 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.348-552C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337557 | |||||||
| chr11:18337679 | GTTA | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(50): Show |
75 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.348-422_348-420del others(3): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 18337679 | ||||||
| chr11:18337764 | C | T | 3 | a0002c0003t0002g0153 a0002c0003t0002g0157 a0002c0003t0007g0152 |
3 | NA18942.hp1 NA18946.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.348-345C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337764 | |||||||
| chr11:18337852 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.348-257A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18337852 | |||||||
| chr11:18338058 | T | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0270 |
2 | HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.348-51T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 3/14 | chr11 | 18338058 | |||||||
| chr11:18338323 | A | G | 1 | a0001c0001t0004g0216 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.513+49A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338323 | |||||||
| chr11:18338364 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.513+90A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338364 | |||||||
| chr11:18338383 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.513+109A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338383 | |||||||
| chr11:18338436 | ATGTT | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.513+180_513+183del others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 18338436 | ||||||
| chr11:18338442 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513+168G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338442 | |||||||
| chr11:18338584 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.513+310G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338584 | |||||||
| chr11:18338626 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.513+352T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338626 | |||||||
| chr11:18338704 | C | T | 105 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(102): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.513+430C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338704 | |||||||
| chr11:18338814 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.513+540T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18338814 | |||||||
| chr11:18339003 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.514-561T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339003 | |||||||
| chr11:18339114 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-450A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339114 | |||||||
| chr11:18339256 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.514-308A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339256 | |||||||
| chr11:18339302 | T | A | 1 | a0001c0001t0002g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.514-262T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339302 | |||||||
| chr11:18339382 | G | A | 2 | a0001c0001t0002g0093 a0001c0001t0002g0101 |
2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.514-182G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339382 | |||||||
| chr11:18339386 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.514-178G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339386 | |||||||
| chr11:18339428 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.514-136G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339428 | |||||||
| chr11:18339429 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.514-135T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 4/14 | chr11 | 18339429 | |||||||
| chr11:18339713 | T | C | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01070.hp2 HG01433.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.607+56T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18339713 | |||||||
| chr11:18339829 | T | G | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+172T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18339829 | |||||||
| chr11:18340042 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.607+385A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340042 | |||||||
| chr11:18340288 | C | CT | 25 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(22): Show |
26 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.607+644dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 18340288 | ||||||
| chr11:18340425 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.607+768C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340425 | |||||||
| chr11:18340534 | C | T | 1 | a0001c0001t0004g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.608-727C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340534 | |||||||
| chr11:18340582 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.608-679C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340582 | |||||||
| chr11:18340585 | G | T | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-676G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340585 | |||||||
| chr11:18340687 | G | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.608-574G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340687 | |||||||
| chr11:18340835 | T | G | 1 | a0001c0001t0001g0020 | 2 | NA18943.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.608-426T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340835 | |||||||
| chr11:18340846 | A | G | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-415A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340846 | |||||||
| chr11:18340910 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
60 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.608-351A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340910 | |||||||
| chr11:18340940 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.608-321A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340940 | |||||||
| chr11:18340973 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.608-288G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340973 | |||||||
| chr11:18340978 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.608-283C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340978 | |||||||
| chr11:18340982 | G | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.608-279G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18340982 | |||||||
| chr11:18341231 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-30T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 5/14 | chr11 | 18341231 | |||||||
| chr11:18341639 | AAG | A | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(11): Show |
14 | HG02451.hp1 HG02738.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+35_837+36delAG | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18341639 | ||||||
| chr11:18341712 | G | A | 1 | a0001c0002t0004g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.837+105G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18341712 | |||||||
| chr11:18342022 | C | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(143): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.837+415C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342022 | |||||||
| chr11:18342070 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.837+463C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342070 | |||||||
| chr11:18342185 | T | C | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02965.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+578T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342185 | |||||||
| chr11:18342252 | C | CT | 10 | a0001c0001t0001g0019 a0001c0001t0001g0239 a0001c0001t0001g0243 others(7): Show |
11 | HG01074.hp1 HG01175.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+672dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342252 | CT | C | 22 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(19): Show |
22 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.837+672delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342252 | CTT | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(48): Show |
76 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.837+671_837+672del others(2): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342252 | CTTT | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
83 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+670_837+672del others(3): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342252 | CTTTT | C | 85 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0189 others(82): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.837+669_837+672del others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342252 | CTTTTT | C | 11 | a0001c0001t0002g0039 a0001c0001t0002g0094 a0001c0001t0002g0102 others(8): Show |
11 | HG00323.hp1 HG00609.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+668_837+672del others(5): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342252 | CTTTTTTT others(10): Show |
C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+656_837+672del others(17): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342252 | ||||||
| chr11:18342259 | T | TG | 5 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0279 others(2): Show |
6 | HG02615.hp1 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+652_837+653ins others(1): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342259 | |||||||
| chr11:18342260 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.837+653T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342260 | |||||||
| chr11:18342341 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0161 others(15): Show |
25 | HG00423.hp2 HG00621.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.837+734A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342341 | |||||||
| chr11:18342506 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.837+899C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342506 | |||||||
| chr11:18342593 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.837+986A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342593 | |||||||
| chr11:18342638 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+1031T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342638 | |||||||
| chr11:18342732 | CT | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+1134delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18342732 | ||||||
| chr11:18342811 | G | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(202): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.837+1204G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18342811 | |||||||
| chr11:18343036 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | NA18944.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.837+1429C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343036 | |||||||
| chr11:18343047 | G | A | 12 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0087 others(9): Show |
19 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.837+1440G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343047 | |||||||
| chr11:18343122 | A | G | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02965.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+1515A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343122 | |||||||
| chr11:18343174 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.837+1567G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343174 | |||||||
| chr11:18343358 | T | G | 1 | a0001c0001t0002g0101 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.837+1751T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343358 | |||||||
| chr11:18343481 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.837+1874C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343481 | |||||||
| chr11:18343555 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.837+1948C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343555 | |||||||
| chr11:18343567 | A | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.837+1960A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343567 | |||||||
| chr11:18343683 | C | T | 8 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(5): Show |
8 | HG02451.hp1 HG02738.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+2076C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343683 | |||||||
| chr11:18343860 | G | A | 9 | a0001c0001t0003g0011 a0001c0001t0003g0045 a0001c0001t0003g0194 others(6): Show |
12 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.837+2253G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343860 | |||||||
| chr11:18343875 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+2268C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343875 | |||||||
| chr11:18343906 | T | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+2299T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18343906 | |||||||
| chr11:18344000 | A | AT | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+2399dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18344000 | ||||||
| chr11:18344163 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(239): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.837+2556A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344163 | |||||||
| chr11:18344184 | T | G | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.837+2577T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344184 | |||||||
| chr11:18344199 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.837+2592C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344199 | |||||||
| chr11:18344257 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.837+2650T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344257 | |||||||
| chr11:18344303 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.837+2696G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344303 | |||||||
| chr11:18344321 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(143): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.837+2714G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344321 | |||||||
| chr11:18344391 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+2784G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344391 | |||||||
| chr11:18344576 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0038 a0001c0001t0002g0208 |
4 | NA18951.hp2 NA18968.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+2969A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344576 | |||||||
| chr11:18344616 | CA | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(41): Show |
64 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.838-2952delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18344616 | ||||||
| chr11:18344616 | CAA | C | 171 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(168): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.838-2953_838-2952d others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18344616 | ||||||
| chr11:18344821 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.838-2767C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344821 | |||||||
| chr11:18344863 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.838-2725A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344863 | |||||||
| chr11:18344932 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0030 others(11): Show |
19 | HG01074.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.838-2656G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344932 | |||||||
| chr11:18344997 | T | C | 1 | a0001c0001t0004g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.838-2591T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18344997 | |||||||
| chr11:18345018 | CT | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.838-2557delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345018 | ||||||
| chr11:18345086 | G | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.838-2502G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345086 | |||||||
| chr11:18345096 | TAGGAGGA others(12): Show |
T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.838-2485_838-2467d others(21): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345096 | ||||||
| chr11:18345200 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.838-2388T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345200 | |||||||
| chr11:18345499 | C | CT | 12 | a0001c0001t0001g0043 a0001c0001t0001g0238 a0001c0001t0003g0011 others(9): Show |
17 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.838-2072dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345499 | ||||||
| chr11:18345499 | C | CTTT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(4): Show |
9 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-2074_838-2072d others(5): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345499 | ||||||
| chr11:18345579 | A | G | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02080.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.838-2009A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345579 | |||||||
| chr11:18345583 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(143): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.838-2005C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345583 | |||||||
| chr11:18345633 | G | A | 1 | a0001c0001t0010g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.838-1955G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345633 | |||||||
| chr11:18345796 | G | GTCTTTTT others(2): Show |
115 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0187 others(112): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.838-1791_838-1790i others(11): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345796 | ||||||
| chr11:18345796 | G | GTCTTTTT others(3): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(46): Show |
71 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.838-1791_838-1790i others(12): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345796 | ||||||
| chr11:18345796 | G | GTCTTTTT others(4): Show |
44 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
58 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.838-1791_838-1790i others(13): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345796 | ||||||
| chr11:18345796 | G | GTCTTTTT others(5): Show |
4 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0203 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-1791_838-1790i others(14): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18345796 | ||||||
| chr11:18345815 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0103 a0001c0001t0002g0108 others(1): Show |
7 | HG02135.hp1 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-1773G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345815 | |||||||
| chr11:18345878 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.838-1710C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345878 | |||||||
| chr11:18345923 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.838-1665T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18345923 | |||||||
| chr11:18346004 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.838-1584A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18346004 | |||||||
| chr11:18346072 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.838-1516A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18346072 | |||||||
| chr11:18346180 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.838-1408T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18346180 | |||||||
| chr11:18346733 | C | CT | 22 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0035 others(19): Show |
26 | HG00639.hp1 HG01074.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.838-833dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18346733 | ||||||
| chr11:18346733 | C | CTT | 157 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(154): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.838-834_838-833dup others(2): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18346733 | ||||||
| chr11:18346733 | C | CTTT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(59): Show |
85 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.838-835_838-833dup others(3): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 18346733 | ||||||
| chr11:18347031 | A | G | 9 | a0001c0001t0003g0011 a0001c0001t0003g0045 a0001c0001t0003g0194 others(6): Show |
12 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.838-557A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347031 | |||||||
| chr11:18347037 | T | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.838-551T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347037 | |||||||
| chr11:18347096 | C | T | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(11): Show |
14 | HG02451.hp1 HG02738.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.838-492C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347096 | |||||||
| chr11:18347129 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
60 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.838-459T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347129 | |||||||
| chr11:18347218 | C | A | 1 | a0001c0001t0003g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838-370C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347218 | |||||||
| chr11:18347230 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.838-358C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347230 | |||||||
| chr11:18347306 | G | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.838-282G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 7/14 | chr11 | 18347306 | |||||||
| chr11:18347758 | A | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0137 |
4 | HG00735.hp1 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+43A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 8/14 | chr11 | 18347758 | |||||||
| chr11:18347764 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.965+49A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 8/14 | chr11 | 18347764 | |||||||
| chr11:18347803 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.966-29G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 8/14 | chr11 | 18347803 | |||||||
| chr11:18348054 | T | A | 1 | a0001c0001t0002g0111 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1053+135T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348054 | |||||||
| chr11:18348064 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1053+145C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348064 | |||||||
| chr11:18348098 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1053+179A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348098 | |||||||
| chr11:18348139 | T | TTTTG | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1053+240_1053+243d others(6): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18348139 | ||||||
| chr11:18348178 | A | G | 6 | a0001c0001t0003g0011 a0001c0001t0003g0045 a0001c0001t0003g0197 others(3): Show |
9 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1053+259A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348178 | |||||||
| chr11:18348755 | A | G | 10 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(7): Show |
15 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1053+836A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348755 | |||||||
| chr11:18348770 | T | C | 2 | a0001c0001t0003g0194 a0001c0001t0003g0198 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1053+851T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348770 | |||||||
| chr11:18348800 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1053+881C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348800 | |||||||
| chr11:18348882 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0208 |
2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1053+963A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348882 | |||||||
| chr11:18348938 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1053+1019G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348938 | |||||||
| chr11:18348952 | C | T | 11 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(8): Show |
12 | HG00558.hp1 HG01952.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1053+1033C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348952 | |||||||
| chr11:18348975 | AC | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053+1057delC | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18348975 | |||||||
| chr11:18349192 | C | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1053+1273C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349192 | |||||||
| chr11:18349289 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1053+1370A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349289 | |||||||
| chr11:18349351 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1053+1432G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349351 | |||||||
| chr11:18349388 | T | C | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0155 others(1): Show |
4 | NA18949.hp2 NA18982.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+1469T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349388 | |||||||
| chr11:18349422 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(143): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1053+1503C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349422 | |||||||
| chr11:18349703 | A | AT | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053+1787dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18349703 | ||||||
| chr11:18349790 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053+1871C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349790 | |||||||
| chr11:18349843 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1053+1924G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349843 | |||||||
| chr11:18349889 | G | C | 1 | a0001c0004t0002g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1053+1970G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18349889 | |||||||
| chr11:18350013 | A | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1054-1868A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18350013 | |||||||
| chr11:18350281 | A | C | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1054-1600A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18350281 | |||||||
| chr11:18350438 | TA | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1054-1431delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18350438 | ||||||
| chr11:18350476 | T | G | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1054-1405T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18350476 | |||||||
| chr11:18350483 | CTGAGGTC others(100): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1054-1311_1054-120 others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18350483 | ||||||
| chr11:18351143 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1054-738G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351143 | |||||||
| chr11:18351227 | G | GAAAAAAA others(1): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054-651_1054-644d others(10): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18351227 | ||||||
| chr11:18351237 | A | AAAAAAAA others(1): Show |
7 | a0001c0001t0001g0029 a0001c0001t0001g0263 a0001c0001t0001g0277 others(4): Show |
8 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-644_1054-643i others(10): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351237 | |||||||
| chr11:18351237 | A | AAAAAAAT others(1): Show |
7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(4): Show |
7 | HG02738.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054-644_1054-643i others(10): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351237 | |||||||
| chr11:18351237 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1054-644A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351237 | |||||||
| chr11:18351285 | A | AT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(192): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1054-579dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18351285 | ||||||
| chr11:18351285 | A | ATT | 18 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0079 others(15): Show |
19 | HG00621.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1054-580_1054-579d others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 18351285 | ||||||
| chr11:18351297 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054-584T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351297 | |||||||
| chr11:18351434 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1054-447G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351434 | |||||||
| chr11:18351818 | G | A | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054-63G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 9/14 | chr11 | 18351818 | |||||||
| chr11:18352060 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1142+91C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 10/14 | chr11 | 18352060 | |||||||
| chr11:18352209 | C | T | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-120C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 10/14 | chr11 | 18352209 | |||||||
| chr11:18352244 | G | A | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-85G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 10/14 | chr11 | 18352244 | |||||||
| chr11:18352547 | C | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1260+101C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352547 | |||||||
| chr11:18352647 | A | G | 26 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
27 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1260+201A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352647 | |||||||
| chr11:18352703 | A | C | 1 | a0001c0001t0002g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1260+257A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352703 | |||||||
| chr11:18352732 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1260+286G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352732 | |||||||
| chr11:18352790 | C | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1260+344C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352790 | |||||||
| chr11:18352878 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1260+432T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352878 | |||||||
| chr11:18352961 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1260+515C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352961 | |||||||
| chr11:18352967 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1260+521T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18352967 | |||||||
| chr11:18353235 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(233): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1260+789G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353235 | |||||||
| chr11:18353397 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1260+951A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353397 | |||||||
| chr11:18353463 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1260+1017A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353463 | |||||||
| chr11:18353617 | A | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1260+1171A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353617 | |||||||
| chr11:18353650 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1260+1204C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353650 | |||||||
| chr11:18353821 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
12 | HG01891.hp1 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+1375A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353821 | |||||||
| chr11:18353889 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0182 |
2 | NA18986.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1260+1443G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353889 | |||||||
| chr11:18353986 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1260+1540G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18353986 | |||||||
| chr11:18354023 | T | G | 1 | a0001c0001t0002g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1260+1577T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354023 | |||||||
| chr11:18354109 | G | C | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1260+1663G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354109 | |||||||
| chr11:18354175 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0161 others(15): Show |
25 | HG00423.hp2 HG00621.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260+1729C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354175 | |||||||
| chr11:18354197 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(281): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1260+1751C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354197 | |||||||
| chr11:18354601 | C | G | 1 | a0001c0001t0002g0133 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1260+2155C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354601 | |||||||
| chr11:18354676 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1260+2230C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354676 | |||||||
| chr11:18354894 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1260+2448C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354894 | |||||||
| chr11:18354933 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1260+2487C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18354933 | |||||||
| chr11:18355057 | G | A | 3 | a0001c0001t0002g0114 a0001c0001t0002g0122 a0001c0001t0002g0134 |
3 | HG01071.hp1 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1260+2611G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355057 | |||||||
| chr11:18355115 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1260+2669A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355115 | |||||||
| chr11:18355205 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1261-2747T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355205 | |||||||
| chr11:18355287 | C | T | 1 | a0001c0001t0010g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1261-2665C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355287 | |||||||
| chr11:18355425 | G | C | 4 | a0001c0001t0002g0115 a0001c0001t0008g0104 a0001c0001t0008g0160 others(1): Show |
4 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-2527G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355425 | |||||||
| chr11:18355484 | A | AAAAT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1261-2455_1261-245 others(8): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18355484 | ||||||
| chr11:18355490 | A | AATAT | 10 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(7): Show |
15 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1261-2459_1261-245 others(8): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18355490 | ||||||
| chr11:18355524 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1261-2428G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355524 | |||||||
| chr11:18355666 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1261-2286A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355666 | |||||||
| chr11:18355695 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1261-2257T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355695 | |||||||
| chr11:18355871 | G | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1261-2081G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18355871 | |||||||
| chr11:18356036 | G | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1916G>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356036 | |||||||
| chr11:18356182 | A | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0001g0081 |
3 | HG02132.hp2 NA19084.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1261-1770A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356182 | |||||||
| chr11:18356249 | G | A | 11 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(8): Show |
12 | HG00558.hp1 HG01952.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-1703G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356249 | |||||||
| chr11:18356319 | A | G | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1633A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356319 | |||||||
| chr11:18356377 | C | CA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0032 others(25): Show |
34 | HG00423.hp1 HG00639.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.1261-1554dupA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18356377 | ||||||
| chr11:18356377 | CA | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(40): Show |
57 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1261-1554delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18356377 | ||||||
| chr11:18356439 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1261-1513A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356439 | |||||||
| chr11:18356521 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1261-1431G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356521 | |||||||
| chr11:18356555 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1261-1397G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356555 | |||||||
| chr11:18356787 | GT | G | 40 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0074 others(37): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1261-1146delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18356787 | ||||||
| chr11:18356787 | GTT | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(198): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1261-1147_1261-114 others(6): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18356787 | ||||||
| chr11:18356796 | T | G | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1261-1156T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356796 | |||||||
| chr11:18356821 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1261-1131G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356821 | |||||||
| chr11:18356946 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1261-1006A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356946 | |||||||
| chr11:18356953 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1261-999A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356953 | |||||||
| chr11:18356967 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1261-985A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18356967 | |||||||
| chr11:18357115 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1261-837A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18357115 | |||||||
| chr11:18357137 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1261-815A>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18357137 | |||||||
| chr11:18357225 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-727C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18357225 | |||||||
| chr11:18357336 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0024 others(31): Show |
45 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1261-616A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18357336 | |||||||
| chr11:18357846 | GA | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0167 a0001c0001t0001g0170 |
4 | HG01516.hp1 HG01517.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-102delA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 18357846 | ||||||
| chr11:18357911 | A | G | 1 | a0001c0001t0014g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1261-41A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18357911 | |||||||
| chr11:18357929 | T | G | 1 | a0001c0001t0002g0206 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1261-23T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 11/14 | chr11 | 18357929 | |||||||
| chr11:18358082 | C | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(202): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1351+40C>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 12/14 | chr11 | 18358082 | |||||||
| chr11:18358292 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1352-233T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 12/14 | chr11 | 18358292 | |||||||
| chr11:18358318 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352-207A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 12/14 | chr11 | 18358318 | |||||||
| chr11:18358376 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0031 |
3 | HG01243.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1352-149A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 12/14 | chr11 | 18358376 | |||||||
| chr11:18358473 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(5): Show |
10 | HG01070.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352-52C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 12/14 | chr11 | 18358473 | |||||||
| chr11:18358519 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG03486.hp2 | splice_region_variant&intron_variant | LOW | c.1352-6T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 12/14 | chr11 | 18358519 | |||||||
| chr11:18358760 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1467+120A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18358760 | |||||||
| chr11:18358824 | T | C | 1 | a0001c0001t0004g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1467+184T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18358824 | |||||||
| chr11:18358877 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1467+237C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18358877 | |||||||
| chr11:18358921 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1467+281A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18358921 | |||||||
| chr11:18359046 | A | G | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1467+406A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18359046 | |||||||
| chr11:18359288 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1467+648C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18359288 | |||||||
| chr11:18359312 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1467+672G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18359312 | |||||||
| chr11:18359780 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1468-835T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18359780 | |||||||
| chr11:18359804 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG01074.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1468-811G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18359804 | |||||||
| chr11:18359871 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0137 |
4 | HG00735.hp1 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-744G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18359871 | |||||||
| chr11:18360156 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1468-459C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18360156 | |||||||
| chr11:18360201 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1468-414C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18360201 | |||||||
| chr11:18360227 | AT | A | 105 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(102): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1468-384delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 18360227 | ||||||
| chr11:18360247 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1468-368T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18360247 | |||||||
| chr11:18360413 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1468-202G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18360413 | |||||||
| chr11:18360447 | T | A | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1468-168T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18360447 | |||||||
| chr11:18360474 | A | G | 105 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(102): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1468-141A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 13/14 | chr11 | 18360474 | |||||||
| chr11:18360807 | C | CT | 9 | a0001c0001t0001g0235 a0001c0001t0001g0242 a0001c0001t0001g0243 others(6): Show |
9 | HG01934.hp2 HG01981.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.1560+116dupT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 18360807 | ||||||
| chr11:18360807 | CT | C | 9 | a0001c0001t0001g0085 a0001c0001t0001g0171 a0001c0001t0001g0179 others(6): Show |
9 | HG01070.hp1 HG01167.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1560+116delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 18360807 | ||||||
| chr11:18360993 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1560+286C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18360993 | |||||||
| chr11:18361202 | AAAT | A | 3 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0219 |
3 | HG02145.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1560+498_1560+500d others(5): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 18361202 | ||||||
| chr11:18361364 | C | T | 61 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0015 others(58): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.1560+657C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361364 | |||||||
| chr11:18361376 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1560+669T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361376 | |||||||
| chr11:18361409 | G | A | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1560+702G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361409 | |||||||
| chr11:18361424 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1560+717T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361424 | |||||||
| chr11:18361567 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1560+860G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361567 | |||||||
| chr11:18361600 | CAG | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0002g0008 others(3): Show |
10 | HG02135.hp1 HG02818.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.1560+894_1560+895d others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361600 | |||||||
| chr11:18361763 | G | A | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1560+1056G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361763 | |||||||
| chr11:18361854 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1560+1147G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361854 | |||||||
| chr11:18361902 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1560+1195T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18361902 | |||||||
| chr11:18362037 | A | G | 12 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0088 others(9): Show |
16 | HG02132.hp1 HG02135.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+1330A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362037 | |||||||
| chr11:18362046 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1560+1339A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362046 | |||||||
| chr11:18362208 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
60 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1560+1501G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362208 | |||||||
| chr11:18362333 | T | G | 1 | a0001c0001t0002g0116 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1560+1626T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362333 | |||||||
| chr11:18362493 | A | G | 1 | a0001c0001t0003g0017 | 3 | HG02622.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1560+1786A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362493 | |||||||
| chr11:18362527 | T | C | 1 | a0001c0001t0004g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1560+1820T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362527 | |||||||
| chr11:18362623 | C | G | 105 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(102): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1560+1916C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362623 | |||||||
| chr11:18362656 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1560+1949T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362656 | |||||||
| chr11:18362668 | CT | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1560+1981delT | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 18362668 | ||||||
| chr11:18362668 | CTT | C | 15 | a0001c0001t0001g0171 a0001c0001t0001g0266 a0001c0001t0002g0117 others(12): Show |
20 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1560+1980_1560+198 others(6): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 18362668 | ||||||
| chr11:18362675 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(191): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1560+1968T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362675 | |||||||
| chr11:18362676 | T | C | 3 | a0001c0001t0001g0171 a0001c0001t0002g0117 a0001c0001t0002g0214 |
3 | NA18971.hp1 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1560+1969T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362676 | |||||||
| chr11:18362724 | G | A | 15 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0088 others(12): Show |
19 | HG02132.hp1 HG02135.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.1560+2017G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362724 | |||||||
| chr11:18362795 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0271 others(11): Show |
16 | HG01070.hp2 HG01433.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+2088C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362795 | |||||||
| chr11:18362956 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0192 |
5 | HG00597.hp2 NA18945.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1560+2249A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362956 | |||||||
| chr11:18362986 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1560+2279A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18362986 | |||||||
| chr11:18363244 | C | T | 1 | a0001c0001t0014g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1560+2537C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363244 | |||||||
| chr11:18363245 | G | A | 2 | a0001c0002t0001g0222 a0001c0002t0004g0220 |
2 | HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1560+2538G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363245 | |||||||
| chr11:18363260 | A | T | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0216 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561-2523A>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363260 | |||||||
| chr11:18363266 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1561-2517C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363266 | |||||||
| chr11:18363336 | T | C | 9 | a0001c0001t0003g0011 a0001c0001t0003g0045 a0001c0001t0003g0194 others(6): Show |
12 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1561-2447T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363336 | |||||||
| chr11:18363391 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1561-2392A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363391 | |||||||
| chr11:18363429 | A | G | 6 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0073 others(3): Show |
6 | HG02132.hp2 NA18992.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561-2354A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363429 | |||||||
| chr11:18363576 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
60 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1561-2207T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363576 | |||||||
| chr11:18363672 | C | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
59 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1561-2111C>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363672 | |||||||
| chr11:18363756 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1561-2027A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363756 | |||||||
| chr11:18363766 | G | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0088 others(9): Show |
16 | HG02132.hp1 HG02135.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.1561-2017G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363766 | |||||||
| chr11:18363870 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1561-1913C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363870 | |||||||
| chr11:18363967 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1561-1816G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18363967 | |||||||
| chr11:18364200 | A | G | 1 | a0001c0001t0004g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1561-1583A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364200 | |||||||
| chr11:18364209 | T | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1561-1574T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364209 | |||||||
| chr11:18364253 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1561-1530G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364253 | |||||||
| chr11:18364303 | A | G | 1 | a0001c0001t0004g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1561-1480A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364303 | |||||||
| chr11:18364399 | A | G | 4 | a0001c0001t0002g0115 a0001c0001t0008g0104 a0001c0001t0008g0160 others(1): Show |
4 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561-1384A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364399 | |||||||
| chr11:18364443 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1561-1340C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364443 | |||||||
| chr11:18364519 | T | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0045 others(8): Show |
16 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1561-1264T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364519 | |||||||
| chr11:18364783 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1561-1000T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364783 | |||||||
| chr11:18364822 | T | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1561-961T>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364822 | |||||||
| chr11:18364887 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1561-896G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364887 | |||||||
| chr11:18364964 | T | C | 1 | a0001c0001t0014g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1561-819T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18364964 | |||||||
| chr11:18365035 | G | C | 2 | a0001c0001t0009g0099 a0002c0003t0002g0157 |
2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1561-748G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365035 | |||||||
| chr11:18365040 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1561-743G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365040 | |||||||
| chr11:18365070 | T | TA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
116 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.1561-713_1561-712i others(3): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365070 | |||||||
| chr11:18365070 | T | TAA | 10 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0051 others(7): Show |
10 | HG01952.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1561-713_1561-712i others(4): Show |
GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365070 | |||||||
| chr11:18365071 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(192): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1561-712T>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365071 | |||||||
| chr11:18365071 | T | TA | 40 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(37): Show |
46 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(43): Show |
intron_variant | MODIFIER | c.1561-706dupA | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 18365071 | ||||||
| chr11:18365078 | G | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1561-705G>A | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365078 | |||||||
| chr11:18365085 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1561-698A>G | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365085 | |||||||
| chr11:18365314 | G | C | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561-469G>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365314 | |||||||
| chr11:18365534 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1561-249T>C | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365534 | |||||||
| chr11:18365568 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1561-215C>T | GTF2H1 | ENSG00000110768.12 | transcript | ENST00000265963.9 | protein_coding | 14/14 | chr11 | 18365568 |