Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2967 |
| ensemblid | ENSG00000111358.14 |
| hgncid | 4657 |
| symbol | GTF2H3 |
| name | general transcription factor IIH subunit 3 |
| refseq_nuc | NM_001516.5 |
| refseq_prot | NP_001507.2 |
| ensembl_nuc | ENST00000543341.7 |
| ensembl_prot | ENSP00000445162.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 123633829 |
| end | 123662604 |
| strand | + |
| ver | v1.2 |
| region | chr12:123633829-123662604 |
| region5000 | chr12:123628829-123667604 |
| regionname0 | GTF2H3_chr12_123633829_123662604 |
| regionname5000 | GTF2H3_chr12_123628829_123667604 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 308 | 271 | 92 | 51 | 70 | 18 | 38 | 42 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | MVSDE others(303): Show |
chr12 | 123628829 | 123667604 |
| a0002 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | MN | chr12 | 123628829 | 123667604 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 924 | 167 | 36 | 29 | 63 | 11 | 26 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ATGGT others(919): Show |
chr12 | 123628829 | 123667604 | ||
| a0001c0002 | 0/0 | 924 | 92 | 49 | 19 | 7 | 7 | 10 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ATGGT others(919): Show |
chr12 | 123628829 | 123667604 | ||
| a0001c0003 | 0/0 | 924 | 10 | 5 | 3 | 0 | 0 | 2 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ATGGT others(919): Show |
chr12 | 123628829 | 123667604 | ||
| a0001c0004 | 0/0 | 924 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ATGGT others(919): Show |
chr12 | 123628829 | 123667604 | ||
| a0002c0005 | 0/0 | 924 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ATAGT others(919): Show |
chr12 | 123628829 | 123667604 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3327 | 147 | 35 | 27 | 52 | 11 | 20 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0008 | 0/0 | 3326 | 4 | 1 | 0 | 0 | 0 | 3 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3321): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0009 | 0/0 | 3328 | 3 | 0 | 1 | 0 | 0 | 2 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3323): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0010 | 0/0 | 3327 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0015 | 0/0 | 3323 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3318): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0016 | 0/0 | 3328 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3323): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0017 | 0/0 | 3326 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3321): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0027 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0030 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0031 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0001t0032 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3318): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0002 | 0/0 | 3327 | 44 | 9 | 13 | 7 | 5 | 10 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0003 | 0/0 | 3338 | 12 | 11 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3333): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0005 | 0/0 | 3340 | 7 | 5 | 2 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3335): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0006 | 0/0 | 3338 | 7 | 6 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3333): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0007 | 0/0 | 3338 | 5 | 5 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3333): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0011 | 0/0 | 3340 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3335): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0012 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3337): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0013 | 0/0 | 3339 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3334): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0014 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3334): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0018 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3334): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0022 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3337): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0023 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3334): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0025 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3332): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0026 | 0/0 | 3340 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3335): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0028 | 0/0 | 3328 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3323): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0029 | 0/0 | 3326 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3321): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0033 | 0/0 | 3327 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0034 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0002t0035 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| a0001c0003t0004 | 0/0 | 3340 | 7 | 4 | 1 | 0 | 0 | 2 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3335): Show |
chr12 | 123628829 | 123667604 |
| a0001c0003t0019 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3337): Show |
chr12 | 123628829 | 123667604 |
| a0001c0003t0020 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3336): Show |
chr12 | 123628829 | 123667604 |
| a0001c0003t0021 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3334): Show |
chr12 | 123628829 | 123667604 |
| a0001c0004t0014 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3334): Show |
chr12 | 123628829 | 123667604 |
| a0001c0004t0024 | 0/0 | 3340 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3335): Show |
chr12 | 123628829 | 123667604 |
| a0002c0005t0001 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | ACTTG others(3322): Show |
chr12 | 123628829 | 123667604 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 5 | 15 | 4 | 4 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 1 | 1 | 2 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0007 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0028 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0010g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0015g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0016g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0017g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0027g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0030g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0031g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0001t0032g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0003 | 0/0 | 7 | 0 | 3 | 0 | 0 | 4 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0018g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0023g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0025g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0026g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0028g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0029g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0033g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0034g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0002t0035g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0004g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0019g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0020g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0003t0021g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0004t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0001c0004t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| a0002c0005t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0011 | EUR | GBR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0012 | EUR | GBR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0011 | EUR | FIN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00423 | hp2 | a0001 | c0001 | t0027 | g0001 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00673 | hp2 | a0001 | c0001 | t0030 | g0015 | EAS | CHS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01099 | hp2 | a0001 | c0003 | t0020 | g0019 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01109 | hp2 | a0001 | c0003 | t0004 | g0159 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0080 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0147 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01243 | hp2 | a0001 | c0002 | t0006 | g0162 | AMR | PUR | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01256 | hp1 | a0001 | c0003 | t0021 | g0017 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01346 | hp1 | a0001 | c0002 | t0005 | g0052 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01358 | hp2 | a0002 | c0005 | t0001 | g0109 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01361 | hp2 | a0001 | c0001 | t0031 | g0116 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0012 | EUR | IBS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0059 | EUR | IBS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01517 | hp1 | a0001 | c0002 | t0028 | g0012 | EUR | IBS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01884 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01975 | hp2 | a0001 | c0002 | t0023 | g0050 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0047 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0041 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02148 | hp2 | a0001 | c0002 | t0034 | g0003 | AMR | PEL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02257 | hp2 | a0001 | c0002 | t0007 | g0155 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02258 | hp2 | a0001 | c0002 | t0007 | g0157 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02451 | hp2 | a0001 | c0002 | t0014 | g0152 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | KHV | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0128 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0009 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02615 | hp1 | a0001 | c0002 | t0013 | g0151 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0164 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02630 | hp2 | a0001 | c0002 | t0005 | g0048 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0051 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02647 | hp2 | a0001 | c0003 | t0004 | g0043 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0150 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02809 | hp2 | a0001 | c0002 | t0011 | g0081 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02818 | hp1 | a0001 | c0002 | t0011 | g0115 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0118 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0049 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02895 | hp1 | a0001 | c0002 | t0007 | g0161 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0044 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02897 | hp1 | a0001 | c0002 | t0025 | g0160 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02970 | hp1 | a0001 | c0002 | t0012 | g0039 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02976 | hp1 | a0001 | c0004 | t0014 | g0037 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0153 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03098 | hp1 | a0001 | c0002 | t0022 | g0046 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03139 | hp1 | a0001 | c0002 | t0035 | g0005 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0149 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0154 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03225 | hp2 | a0001 | c0002 | t0029 | g0005 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0038 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03486 | hp1 | a0001 | c0004 | t0024 | g0040 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0002 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0103 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0158 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0156 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0067 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0054 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03942 | hp2 | a0001 | c0003 | t0004 | g0017 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0015 | SAS | BEB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04199 | hp2 | a0001 | c0003 | t0004 | g0017 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | YRI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | YRI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18906 | hp2 | a0001 | c0003 | t0019 | g0019 | AFR | YRI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18964 | hp1 | a0001 | c0001 | t0015 | g0024 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18964 | hp2 | a0001 | c0001 | t0015 | g0088 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18979 | hp1 | a0001 | c0001 | t0016 | g0015 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18979 | hp2 | a0001 | c0001 | t0032 | g0031 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18987 | hp2 | a0001 | c0001 | t0017 | g0136 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19012 | hp1 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | LWK | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19043 | hp2 | a0001 | c0002 | t0026 | g0045 | AFR | LWK | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19240 | hp1 | a0001 | c0003 | t0004 | g0042 | AFR | YRI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0083 | AFR | YRI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20805 | hp1 | a0001 | c0002 | t0033 | g0003 | EUR | TSI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02486 | hp2 | a0001 | c0002 | t0013 | g0148 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG02559 | hp2 | a0001 | c0002 | t0006 | g0163 | AFR | ACB | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| HG06807 | hp2 | a0001 | c0002 | t0018 | g0053 | AFR | USA | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0028 | REF | REF | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0097 | REF | REF | GTF2H3_chr12_123628829_123667604 | GTF2H3 | chr12 | 123628829 | 123667604 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123633862 | G | A | 1 | a0002 | 1 | HG01358.hp2 | start_lost | HIGH | c.3G>A | p.Met1? | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/13 | 34/3327 | 3/927 | 1/308 | chr12 | 123633862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123648122 | C | A | 1 | a0001c0004 | 2 | HG02976.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.360C>A | p.Thr120Thr | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/13 | 391/3327 | 360/927 | 120/308 | chr12 | 123648122 | |||
| chr12:123659812 | T | C | 1 | a0001c0003 | 10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
synonymous_variant | LOW | c.702T>C | p.Asp234Asp | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 11/13 | 733/3327 | 702/927 | 234/308 | chr12 | 123659812 | |||
| chr12:123659848 | A | G | 3 | a0001c0002 a0001c0003 a0001c0004 |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
synonymous_variant | LOW | c.738A>G | p.Pro246Pro | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 11/13 | 769/3327 | 738/927 | 246/308 | chr12 | 123659848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123660245 | A | C | 1 | a0001c0002t0035 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 10 | chr12 | 123660245 | ||||||
| chr12:123660246 | T | C | 19 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0006 others(16): Show |
55 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*11T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 11 | chr12 | 123660246 | ||||||
| chr12:123660320 | G | C | 1 | a0001c0001t0027 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 85 | chr12 | 123660320 | ||||||
| chr12:123660416 | G | A | 1 | a0001c0002t0018 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*181G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 181 | chr12 | 123660416 | ||||||
| chr12:123660614 | A | G | 1 | a0001c0002t0026 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 379 | chr12 | 123660614 | ||||||
| chr12:123660735 | A | G | 1 | a0001c0002t0034 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*500A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 500 | chr12 | 123660735 | ||||||
| chr12:123660999 | G | GA | 9 | a0001c0002t0005 a0001c0002t0011 a0001c0002t0022 others(6): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*772dupA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 773 | INFO_REALIGN_3_PRIME | chr12 | 123660999 | |||||
| chr12:123661104 | C | T | 1 | a0001c0002t0033 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*869C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 869 | chr12 | 123661104 | ||||||
| chr12:123661140 | A | G | 1 | a0001c0002t0034 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*905A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 905 | chr12 | 123661140 | ||||||
| chr12:123661150 | T | C | 25 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(22): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*915T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 915 | chr12 | 123661150 | ||||||
| chr12:123661219 | G | A | 1 | a0001c0001t0030 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*984G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 984 | chr12 | 123661219 | ||||||
| chr12:123661262 | A | T | 1 | a0001c0002t0026 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1027A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1027 | chr12 | 123661262 | ||||||
| chr12:123661275 | C | G | 8 | a0001c0002t0005 a0001c0002t0011 a0001c0002t0022 others(5): Show |
21 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1040C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1040 | chr12 | 123661275 | ||||||
| chr12:123661369 | G | C | 9 | a0001c0002t0005 a0001c0002t0011 a0001c0002t0022 others(6): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1134G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1134 | chr12 | 123661369 | ||||||
| chr12:123661454 | A | G | 4 | a0001c0002t0005 a0001c0002t0011 a0001c0002t0022 others(1): Show |
11 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1219A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1219 | chr12 | 123661454 | ||||||
| chr12:123661501 | C | G | 1 | a0001c0002t0006 | 7 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1266C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1266 | chr12 | 123661501 | ||||||
| chr12:123661640 | C | CA | 5 | a0001c0002t0002 a0001c0002t0028 a0001c0002t0033 others(2): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1417dupA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1418 | INFO_REALIGN_3_PRIME | chr12 | 123661640 | |||||
| chr12:123661640 | C | CAAAAAAA others(4): Show |
2 | a0001c0002t0023 a0001c0002t0025 |
2 | HG01975.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1407_*1417dupAAAA others(7): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1418 | INFO_REALIGN_3_PRIME | chr12 | 123661640 | |||||
| chr12:123661640 | C | CAAAAAAA others(5): Show |
11 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0006 others(8): Show |
45 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1406_*1417dupAAAA others(8): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1418 | INFO_REALIGN_3_PRIME | chr12 | 123661640 | |||||
| chr12:123661640 | C | CAAAAAAA others(6): Show |
5 | a0001c0002t0013 a0001c0002t0018 a0001c0002t0022 others(2): Show |
6 | HG02486.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1417_*1418insAAAA others(9): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1418 | INFO_REALIGN_3_PRIME | chr12 | 123661640 | |||||
| chr12:123661640 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0012 | 2 | HG02970.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1417_*1418insAAAA others(11): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1418 | INFO_REALIGN_3_PRIME | chr12 | 123661640 | |||||
| chr12:123661662 | C | T | 1 | a0001c0001t0032 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1427C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1427 | chr12 | 123661662 | ||||||
| chr12:123661672 | C | T | 1 | a0001c0001t0031 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1437C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1437 | chr12 | 123661672 | ||||||
| chr12:123661845 | C | T | 3 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0017 |
7 | HG00408.hp2 HG02523.hp2 HG04184.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1610C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1610 | chr12 | 123661845 | ||||||
| chr12:123662135 | C | CA | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0002t0022 others(2): Show |
8 | HG01099.hp2 HG01175.hp1 HG02602.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1921dupA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1922 | INFO_REALIGN_3_PRIME | chr12 | 123662135 | |||||
| chr12:123662135 | CA | C | 14 | a0001c0001t0008 a0001c0001t0017 a0001c0002t0002 others(11): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1921delA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1921 | INFO_REALIGN_3_PRIME | chr12 | 123662135 | |||||
| chr12:123662142 | A | G | 2 | a0001c0002t0007 a0001c0002t0025 |
6 | HG02257.hp2 HG02258.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1907A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 1907 | chr12 | 123662142 | ||||||
| chr12:123662429 | T | C | 1 | a0001c0002t0011 | 2 | HG02809.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2194T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 2194 | chr12 | 123662429 | ||||||
| chr12:123662594 | TTTGA | T | 2 | a0001c0001t0015 a0001c0001t0032 |
3 | NA18964.hp1 NA18964.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2362_*2365delGATT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 13/13 | 2362 | INFO_REALIGN_3_PRIME | chr12 | 123662594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123633942 | A | C | 5 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0162 others(2): Show |
7 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+70A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123633942 | |||||||
| chr12:123634231 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.13+359G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634231 | |||||||
| chr12:123634401 | T | C | 18 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(15): Show |
18 | HG01099.hp2 HG01346.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+529T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634401 | |||||||
| chr12:123634432 | C | A | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.13+560C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634432 | |||||||
| chr12:123634608 | A | G | 41 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0149 others(38): Show |
49 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.13+736A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634608 | |||||||
| chr12:123634736 | A | G | 2 | a0001c0002t0007g0161 a0001c0002t0025g0160 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.13+864A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634736 | |||||||
| chr12:123634762 | T | G | 4 | a0001c0002t0012g0038 a0001c0002t0012g0039 a0001c0004t0014g0037 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+890T>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634762 | |||||||
| chr12:123634784 | G | C | 6 | a0001c0003t0004g0041 a0001c0003t0004g0042 a0001c0003t0004g0043 others(3): Show |
6 | HG01099.hp2 HG02145.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+912G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634784 | |||||||
| chr12:123634841 | C | T | 18 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(15): Show |
18 | HG01099.hp2 HG01346.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+969C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123634841 | |||||||
| chr12:123635111 | G | A | 1 | a0001c0001t0009g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.13+1239G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635111 | |||||||
| chr12:123635182 | T | C | 1 | a0001c0002t0013g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.13+1310T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635182 | |||||||
| chr12:123635236 | G | A | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.13+1364G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635236 | |||||||
| chr12:123635342 | G | A | 4 | a0001c0002t0002g0005 a0001c0002t0002g0055 a0001c0002t0029g0005 others(1): Show |
6 | HG02257.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+1470G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635342 | |||||||
| chr12:123635391 | T | C | 18 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(15): Show |
18 | HG01099.hp2 HG01346.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+1519T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635391 | |||||||
| chr12:123635399 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0009g0147 |
3 | HG01099.hp1 HG01175.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.13+1527C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635399 | |||||||
| chr12:123635436 | G | A | 30 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(27): Show |
45 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.13+1564G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635436 | |||||||
| chr12:123635538 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.13+1666A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635538 | |||||||
| chr12:123635570 | C | T | 1 | a0001c0002t0002g0073 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.13+1698C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635570 | |||||||
| chr12:123635572 | C | CA | 21 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0075 others(18): Show |
23 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+1720dupA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123635572 | ||||||
| chr12:123635572 | CA | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(68): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.13+1720delA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123635572 | ||||||
| chr12:123635598 | A | T | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.13+1726A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635598 | |||||||
| chr12:123635658 | C | A | 18 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0149 others(15): Show |
24 | HG01109.hp2 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.13+1786C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635658 | |||||||
| chr12:123635665 | G | A | 18 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(15): Show |
18 | HG01099.hp2 HG01346.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+1793G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635665 | |||||||
| chr12:123635804 | G | A | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.13+1932G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635804 | |||||||
| chr12:123635980 | G | A | 2 | a0001c0002t0012g0038 a0001c0002t0012g0039 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.13+2108G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123635980 | |||||||
| chr12:123636271 | T | C | 1 | a0001c0003t0004g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.13+2399T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636271 | |||||||
| chr12:123636359 | A | T | 6 | a0001c0003t0004g0041 a0001c0003t0004g0042 a0001c0003t0004g0043 others(3): Show |
6 | HG01099.hp2 HG02145.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+2487A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636359 | |||||||
| chr12:123636444 | C | T | 34 | a0001c0001t0001g0032 a0001c0001t0001g0134 a0001c0001t0001g0144 others(31): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.13+2572C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636444 | |||||||
| chr12:123636498 | GGGCACGG others(1): Show |
G | 7 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(4): Show |
7 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+2632_13+2639del others(8): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123636498 | ||||||
| chr12:123636689 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14-2575G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636689 | |||||||
| chr12:123636700 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.14-2564C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636700 | |||||||
| chr12:123636707 | C | T | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14-2557C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636707 | |||||||
| chr12:123636733 | C | T | 1 | a0001c0002t0005g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.14-2531C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636733 | |||||||
| chr12:123636803 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-2461G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636803 | |||||||
| chr12:123636882 | A | T | 5 | a0001c0002t0002g0012 a0001c0002t0002g0071 a0001c0002t0002g0072 others(2): Show |
6 | HG00140.hp1 HG01257.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-2382A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636882 | |||||||
| chr12:123636885 | C | T | 1 | a0001c0001t0001g0014 | 3 | HG01256.hp2 HG01258.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.14-2379C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636885 | |||||||
| chr12:123636927 | A | T | 1 | a0001c0004t0024g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.14-2337A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123636927 | |||||||
| chr12:123637097 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.14-2167A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637097 | |||||||
| chr12:123637444 | T | C | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.14-1820T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637444 | |||||||
| chr12:123637504 | C | CT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(19): Show |
36 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.14-1744dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123637504 | ||||||
| chr12:123637564 | A | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
57 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.14-1700A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637564 | |||||||
| chr12:123637770 | TG | T | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-1491delG | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123637770 | ||||||
| chr12:123637824 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.14-1440C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637824 | |||||||
| chr12:123637839 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.14-1425C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637839 | |||||||
| chr12:123637861 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(18): Show |
35 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-1403G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637861 | |||||||
| chr12:123637875 | T | C | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.14-1389T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123637875 | |||||||
| chr12:123637983 | T | TTTTG | 5 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0162 others(2): Show |
7 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.14-1253_14-1250dup others(4): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123637983 | ||||||
| chr12:123637983 | TTTTG | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(18): Show |
35 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-1253_14-1250del others(4): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123637983 | ||||||
| chr12:123638116 | C | G | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-1148C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638116 | |||||||
| chr12:123638249 | C | T | 1 | a0001c0002t0003g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14-1015C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638249 | |||||||
| chr12:123638325 | A | AT | 23 | a0001c0001t0001g0129 a0001c0002t0002g0072 a0001c0002t0003g0158 others(20): Show |
24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-924dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123638325 | ||||||
| chr12:123638390 | T | C | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-874T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638390 | |||||||
| chr12:123638460 | C | T | 1 | a0001c0002t0005g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.14-804C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638460 | |||||||
| chr12:123638461 | G | A | 4 | a0001c0002t0002g0005 a0001c0002t0002g0055 a0001c0002t0029g0005 others(1): Show |
6 | HG02257.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-803G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638461 | |||||||
| chr12:123638523 | G | A | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-741G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638523 | |||||||
| chr12:123638616 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.14-648C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638616 | |||||||
| chr12:123638792 | C | CT | 26 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0119 others(23): Show |
27 | HG00423.hp1 HG00597.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.14-451dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 123638792 | ||||||
| chr12:123638865 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0074 |
3 | HG00438.hp1 NA18947.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.14-399G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638865 | |||||||
| chr12:123638889 | G | A | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-375G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638889 | |||||||
| chr12:123638909 | G | C | 3 | a0001c0002t0002g0056 a0001c0002t0002g0058 a0001c0002t0002g0059 |
3 | HG01516.hp2 HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.14-355G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638909 | |||||||
| chr12:123638921 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.14-343G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638921 | |||||||
| chr12:123638930 | G | A | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-334G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638930 | |||||||
| chr12:123638997 | G | A | 4 | a0001c0002t0012g0038 a0001c0002t0012g0039 a0001c0004t0014g0037 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-267G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123638997 | |||||||
| chr12:123639017 | G | T | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.14-247G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123639017 | |||||||
| chr12:123639019 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.14-245T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 1/12 | chr12 | 123639019 | |||||||
| chr12:123639509 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+166C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123639509 | |||||||
| chr12:123639598 | G | T | 1 | a0001c0001t0031g0116 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.93+255G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123639598 | |||||||
| chr12:123639817 | A | G | 4 | a0001c0002t0005g0083 a0001c0002t0005g0128 a0001c0002t0011g0081 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+474A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123639817 | |||||||
| chr12:123639894 | C | CGTGT | 17 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(14): Show |
18 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+554_93+555insTG others(2): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123639894 | ||||||
| chr12:123639898 | C | CGTGT | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(79): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.93+556_93+559dupGT others(2): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123639898 | ||||||
| chr12:123639898 | C | T | 17 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(14): Show |
18 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+555C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123639898 | |||||||
| chr12:123640055 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.93+712T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640055 | |||||||
| chr12:123640080 | G | A | 11 | a0001c0002t0003g0149 a0001c0002t0003g0150 a0001c0002t0003g0154 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.93+737G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640080 | |||||||
| chr12:123640178 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(18): Show |
35 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.93+835G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640178 | |||||||
| chr12:123640305 | C | A | 4 | a0001c0002t0005g0083 a0001c0002t0005g0128 a0001c0002t0011g0081 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+962C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640305 | |||||||
| chr12:123640337 | C | CT | 54 | a0001c0001t0001g0131 a0001c0002t0002g0003 a0001c0002t0002g0005 others(51): Show |
77 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.93+1010dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123640337 | ||||||
| chr12:123640337 | CT | C | 20 | a0001c0001t0001g0138 a0001c0002t0005g0047 a0001c0002t0005g0048 others(17): Show |
21 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.93+1010delT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123640337 | ||||||
| chr12:123640360 | G | T | 5 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0162 others(2): Show |
7 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+1017G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640360 | |||||||
| chr12:123640471 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.93+1128G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640471 | |||||||
| chr12:123640486 | G | A | 16 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(13): Show |
21 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.93+1143G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640486 | |||||||
| chr12:123640690 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0142 |
2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.93+1347A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640690 | |||||||
| chr12:123640891 | A | G | 1 | a0001c0002t0013g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.93+1548A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640891 | |||||||
| chr12:123640934 | T | C | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.93+1591T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123640934 | |||||||
| chr12:123641101 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.93+1758A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641101 | |||||||
| chr12:123641178 | A | C | 3 | a0001c0003t0004g0017 a0001c0003t0004g0159 a0001c0003t0021g0017 |
4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1835A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641178 | |||||||
| chr12:123641210 | A | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.93+1867A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641210 | |||||||
| chr12:123641232 | C | CT | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(38): Show |
62 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.93+1901dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123641232 | ||||||
| chr12:123641258 | G | A | 3 | a0001c0003t0004g0017 a0001c0003t0004g0159 a0001c0003t0021g0017 |
4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1915G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641258 | |||||||
| chr12:123641328 | C | T | 9 | a0001c0003t0004g0017 a0001c0003t0004g0041 a0001c0003t0004g0042 others(6): Show |
10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+1985C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641328 | |||||||
| chr12:123641344 | G | C | 1 | a0001c0002t0003g0149 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.93+2001G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641344 | |||||||
| chr12:123641414 | C | T | 18 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0020 others(15): Show |
28 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.93+2071C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641414 | |||||||
| chr12:123641517 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.93+2174G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641517 | |||||||
| chr12:123641527 | G | GT | 4 | a0001c0001t0001g0033 a0001c0002t0002g0072 a0001c0002t0006g0036 others(1): Show |
6 | HG01884.hp1 HG01981.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+2195dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123641527 | ||||||
| chr12:123641537 | T | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0086 others(4): Show |
11 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.93+2194T>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641537 | |||||||
| chr12:123641538 | TG | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0034 others(24): Show |
44 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.93+2196delG | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641538 | |||||||
| chr12:123641539 | G | T | 68 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(65): Show |
89 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.93+2196G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641539 | |||||||
| chr12:123641540 | TG | T | 4 | a0001c0002t0012g0038 a0001c0002t0012g0039 a0001c0004t0014g0037 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+2198delG | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641540 | |||||||
| chr12:123641541 | G | GT | 7 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(4): Show |
7 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+2199dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123641541 | ||||||
| chr12:123641541 | G | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.93+2198G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641541 | |||||||
| chr12:123641543 | G | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(60): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.93+2200G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641543 | |||||||
| chr12:123641616 | A | C | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.93+2273A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641616 | |||||||
| chr12:123641633 | A | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.93+2290A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641633 | |||||||
| chr12:123641642 | TAGC | T | 16 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(13): Show |
17 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.93+2305_93+2307del others(3): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123641642 | ||||||
| chr12:123641792 | C | T | 32 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(29): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.93+2449C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641792 | |||||||
| chr12:123641923 | G | A | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.93+2580G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641923 | |||||||
| chr12:123641999 | G | A | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93+2656G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123641999 | |||||||
| chr12:123642054 | A | G | 2 | a0001c0002t0007g0156 a0001c0002t0007g0157 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.93+2711A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123642054 | |||||||
| chr12:123642105 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.93+2762C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123642105 | |||||||
| chr12:123642177 | C | CT | 57 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(54): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.93+2845dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 123642177 | ||||||
| chr12:123642274 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(96): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.93+2931A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123642274 | |||||||
| chr12:123642855 | C | T | 2 | a0001c0003t0004g0041 a0001c0003t0004g0044 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.94-2600C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123642855 | |||||||
| chr12:123642938 | A | T | 2 | a0001c0002t0003g0016 a0001c0002t0003g0118 |
4 | HG01243.hp1 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-2517A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123642938 | |||||||
| chr12:123642967 | C | T | 3 | a0001c0001t0001g0114 a0001c0003t0004g0041 a0001c0003t0004g0044 |
3 | HG02145.hp1 HG02895.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.94-2488C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123642967 | |||||||
| chr12:123643067 | G | A | 1 | a0001c0002t0005g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-2388G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643067 | |||||||
| chr12:123643178 | C | A | 22 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(19): Show |
29 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.94-2277C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643178 | |||||||
| chr12:123643444 | C | T | 4 | a0001c0002t0005g0048 a0001c0002t0005g0049 a0001c0002t0005g0051 others(1): Show |
4 | HG02630.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-2011C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643444 | |||||||
| chr12:123643445 | G | A | 7 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(4): Show |
7 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-2010G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643445 | |||||||
| chr12:123643530 | A | G | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.94-1925A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643530 | |||||||
| chr12:123643543 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0140 a0001c0001t0001g0143 |
4 | HG01891.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-1912A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643543 | |||||||
| chr12:123643621 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.94-1834C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643621 | |||||||
| chr12:123643776 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94-1679C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643776 | |||||||
| chr12:123643865 | T | TACTC | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.94-1590_94-1589ins others(4): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643865 | |||||||
| chr12:123643877 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.94-1578C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643877 | |||||||
| chr12:123643955 | C | T | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.94-1500C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123643955 | |||||||
| chr12:123644103 | C | T | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.94-1352C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123644103 | |||||||
| chr12:123644203 | T | C | 4 | a0001c0002t0012g0038 a0001c0002t0012g0039 a0001c0004t0014g0037 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-1252T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123644203 | |||||||
| chr12:123644418 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(96): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.94-1037G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123644418 | |||||||
| chr12:123644442 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.94-1013C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123644442 | |||||||
| chr12:123644614 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(18): Show |
35 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.94-841C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123644614 | |||||||
| chr12:123644746 | A | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0079 a0001c0001t0001g0110 others(2): Show |
6 | HG01884.hp2 HG02145.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-709A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123644746 | |||||||
| chr12:123645071 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.94-384T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123645071 | |||||||
| chr12:123645262 | G | A | 32 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(29): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.94-193G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123645262 | |||||||
| chr12:123645377 | C | A | 22 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(19): Show |
29 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.94-78C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123645377 | |||||||
| chr12:123645422 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0132 |
3 | NA18947.hp2 NA19011.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.94-33T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 2/12 | chr12 | 123645422 | |||||||
| chr12:123645581 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(39): Show |
63 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.200+20T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123645581 | |||||||
| chr12:123645838 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.200+277C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123645838 | |||||||
| chr12:123645839 | G | T | 1 | a0001c0002t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.200+278G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123645839 | |||||||
| chr12:123645841 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(96): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.200+280A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123645841 | |||||||
| chr12:123645860 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0120 |
3 | NA18950.hp2 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.200+299T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123645860 | |||||||
| chr12:123645933 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(19): Show |
36 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.200+372C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123645933 | |||||||
| chr12:123646084 | A | G | 1 | a0001c0002t0002g0069 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.200+523A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646084 | |||||||
| chr12:123646255 | C | A | 9 | a0001c0003t0004g0017 a0001c0003t0004g0041 a0001c0003t0004g0042 others(6): Show |
10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.200+694C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646255 | |||||||
| chr12:123646255 | C | CT | 19 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0079 others(16): Show |
20 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.200+712dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 123646255 | ||||||
| chr12:123646255 | CT | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0024 others(22): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.200+712delT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 123646255 | ||||||
| chr12:123646338 | C | T | 1 | a0002c0005t0001g0109 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.200+777C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646338 | |||||||
| chr12:123646502 | T | C | 8 | a0001c0002t0003g0154 a0001c0002t0007g0153 a0001c0002t0007g0155 others(5): Show |
8 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.200+941T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646502 | |||||||
| chr12:123646679 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.200+1118G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646679 | |||||||
| chr12:123646724 | C | T | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.200+1163C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646724 | |||||||
| chr12:123646752 | G | A | 1 | a0001c0001t0031g0116 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.200+1191G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646752 | |||||||
| chr12:123646805 | G | GT | 32 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(29): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.201-1141dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 123646805 | ||||||
| chr12:123646805 | GT | G | 19 | a0001c0001t0001g0075 a0001c0002t0005g0047 a0001c0002t0005g0048 others(16): Show |
20 | HG01099.hp2 HG01109.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.201-1141delT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 123646805 | ||||||
| chr12:123646917 | C | T | 1 | a0001c0004t0014g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.201-1046C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123646917 | |||||||
| chr12:123647045 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.201-918C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647045 | |||||||
| chr12:123647095 | G | A | 3 | a0001c0003t0004g0017 a0001c0003t0004g0159 a0001c0003t0021g0017 |
4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-868G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647095 | |||||||
| chr12:123647107 | C | T | 5 | a0001c0002t0005g0083 a0001c0002t0005g0128 a0001c0002t0011g0081 others(2): Show |
5 | HG02572.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-856C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647107 | |||||||
| chr12:123647152 | C | CA | 34 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0092 others(31): Show |
41 | HG00438.hp1 HG00741.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.201-791dupA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 123647152 | ||||||
| chr12:123647180 | A | C | 32 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(29): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.201-783A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647180 | |||||||
| chr12:123647192 | G | A | 1 | a0001c0003t0004g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201-771G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647192 | |||||||
| chr12:123647218 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.201-745C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647218 | |||||||
| chr12:123647355 | C | G | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.201-608C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647355 | |||||||
| chr12:123647382 | G | A | 32 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(29): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.201-581G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647382 | |||||||
| chr12:123647402 | G | T | 4 | a0001c0002t0005g0083 a0001c0002t0005g0128 a0001c0002t0011g0081 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.201-561G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647402 | |||||||
| chr12:123647413 | A | G | 2 | a0001c0002t0002g0062 a0001c0002t0002g0063 |
2 | NA18977.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.201-550A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647413 | |||||||
| chr12:123647450 | C | T | 21 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(18): Show |
28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.201-513C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647450 | |||||||
| chr12:123647756 | T | C | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201-207T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647756 | |||||||
| chr12:123647787 | G | A | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.201-176G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647787 | |||||||
| chr12:123647819 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.201-144T>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 3/12 | chr12 | 123647819 | |||||||
| chr12:123648256 | C | T | 2 | a0001c0002t0003g0149 a0001c0002t0013g0151 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.364+130C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123648256 | |||||||
| chr12:123648283 | G | A | 7 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(4): Show |
7 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+157G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123648283 | |||||||
| chr12:123648309 | G | A | 9 | a0001c0003t0004g0017 a0001c0003t0004g0041 a0001c0003t0004g0042 others(6): Show |
10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+183G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123648309 | |||||||
| chr12:123648451 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.364+325G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123648451 | |||||||
| chr12:123648843 | G | A | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.364+717G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123648843 | |||||||
| chr12:123648893 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.364+767A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123648893 | |||||||
| chr12:123649190 | A | G | 1 | a0001c0002t0002g0071 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.364+1064A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649190 | |||||||
| chr12:123649279 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.364+1153T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649279 | |||||||
| chr12:123649368 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.364+1242A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649368 | |||||||
| chr12:123649401 | A | G | 3 | a0001c0002t0005g0047 a0001c0002t0005g0052 a0001c0002t0023g0050 |
3 | HG01346.hp1 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.364+1275A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649401 | |||||||
| chr12:123649453 | C | G | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.364+1327C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649453 | |||||||
| chr12:123649701 | A | C | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.365-1293A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649701 | |||||||
| chr12:123649861 | A | T | 1 | a0001c0001t0031g0116 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.365-1133A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649861 | |||||||
| chr12:123649906 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.365-1088A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123649906 | |||||||
| chr12:123650109 | C | T | 71 | a0001c0001t0001g0106 a0001c0002t0002g0003 a0001c0002t0002g0005 others(68): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.365-885C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123650109 | |||||||
| chr12:123650255 | C | T | 5 | a0001c0002t0002g0012 a0001c0002t0002g0071 a0001c0002t0002g0072 others(2): Show |
6 | HG00140.hp1 HG01257.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.365-739C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123650255 | |||||||
| chr12:123650441 | A | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0033 others(33): Show |
49 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.365-553A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 4/12 | chr12 | 123650441 | |||||||
| chr12:123651211 | G | T | 1 | a0001c0002t0012g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.427+155G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651211 | |||||||
| chr12:123651250 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.427+194G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651250 | |||||||
| chr12:123651251 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.427+195C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651251 | |||||||
| chr12:123651253 | C | T | 2 | a0001c0002t0002g0012 a0001c0002t0028g0012 |
3 | HG00140.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.427+197C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651253 | |||||||
| chr12:123651260 | G | A | 1 | a0001c0001t0001g0006 | 5 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+204G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651260 | |||||||
| chr12:123651267 | G | T | 4 | a0001c0002t0012g0038 a0001c0002t0012g0039 a0001c0004t0014g0037 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+211G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651267 | |||||||
| chr12:123651356 | C | T | 1 | a0001c0002t0003g0149 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+300C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651356 | |||||||
| chr12:123651434 | C | T | 11 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(8): Show |
11 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.427+378C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651434 | |||||||
| chr12:123651445 | A | C | 1 | a0001c0001t0008g0103 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.427+389A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651445 | |||||||
| chr12:123651493 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.427+437C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651493 | |||||||
| chr12:123651775 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.427+719G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651775 | |||||||
| chr12:123651819 | C | CA | 5 | a0001c0002t0002g0012 a0001c0002t0002g0071 a0001c0002t0002g0073 others(2): Show |
6 | HG00140.hp1 HG01257.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-699dupA | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 123651819 | ||||||
| chr12:123651835 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0102 |
2 | NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.428-697A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651835 | |||||||
| chr12:123651920 | C | G | 1 | a0001c0002t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.428-612C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123651920 | |||||||
| chr12:123652060 | C | T | 25 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(22): Show |
26 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.428-472C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123652060 | |||||||
| chr12:123652094 | G | A | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428-438G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123652094 | |||||||
| chr12:123652385 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.428-147G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 5/12 | chr12 | 123652385 | |||||||
| chr12:123652850 | G | A | 1 | a0001c0001t0009g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.486+115G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123652850 | |||||||
| chr12:123652871 | A | G | 16 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(13): Show |
21 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.486+136A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123652871 | |||||||
| chr12:123652906 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.486+171C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123652906 | |||||||
| chr12:123652938 | C | T | 31 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(28): Show |
47 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.486+203C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123652938 | |||||||
| chr12:123653071 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0122 |
2 | HG00597.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.486+336G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653071 | |||||||
| chr12:123653230 | G | A | 4 | a0001c0003t0004g0042 a0001c0003t0004g0043 a0001c0003t0019g0019 others(1): Show |
4 | HG01099.hp2 HG02647.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+495G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653230 | |||||||
| chr12:123653381 | G | T | 3 | a0001c0003t0004g0017 a0001c0003t0004g0159 a0001c0003t0021g0017 |
4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+646G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653381 | |||||||
| chr12:123653513 | G | A | 9 | a0001c0003t0004g0017 a0001c0003t0004g0041 a0001c0003t0004g0042 others(6): Show |
10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+778G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653513 | |||||||
| chr12:123653799 | C | T | 79 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(76): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1064C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653799 | |||||||
| chr12:123653809 | G | T | 1 | a0001c0002t0002g0061 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.486+1074G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653809 | |||||||
| chr12:123653875 | G | A | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.487-1049G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123653875 | |||||||
| chr12:123654071 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.487-853A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123654071 | |||||||
| chr12:123654078 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.487-846C>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | chr12 | 123654078 | |||||||
| chr12:123654222 | GTGTT | G | 4 | a0001c0003t0004g0042 a0001c0003t0004g0043 a0001c0003t0019g0019 others(1): Show |
4 | HG01099.hp2 HG02647.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-696_487-693del others(4): Show |
GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 123654222 | ||||||
| chr12:123654315 | A | AT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.487-606dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 123654315 | ||||||
| chr12:123654400 | A | AT | 4 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0162 others(1): Show |
6 | HG01243.hp2 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-520dupT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 123654400 | ||||||
| chr12:123655050 | A | G | 26 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(23): Show |
39 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.561+52A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 8/12 | chr12 | 123655050 | |||||||
| chr12:123655280 | C | T | 6 | a0001c0002t0007g0153 a0001c0002t0007g0155 a0001c0002t0007g0156 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+282C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 8/12 | chr12 | 123655280 | |||||||
| chr12:123655388 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.562-383C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 8/12 | chr12 | 123655388 | |||||||
| chr12:123655579 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.562-192G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 8/12 | chr12 | 123655579 | |||||||
| chr12:123655840 | A | G | 1 | a0001c0002t0007g0156 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.615+16A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123655840 | |||||||
| chr12:123655855 | G | A | 4 | a0001c0002t0012g0038 a0001c0002t0012g0039 a0001c0004t0014g0037 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+31G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123655855 | |||||||
| chr12:123655856 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0015g0088 |
2 | HG02080.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.615+32G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123655856 | |||||||
| chr12:123655941 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0132 |
5 | HG02155.hp2 NA18947.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+117G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123655941 | |||||||
| chr12:123655965 | C | G | 3 | a0001c0002t0003g0016 a0001c0002t0003g0118 a0001c0002t0003g0158 |
5 | HG01243.hp1 HG02818.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+141C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123655965 | |||||||
| chr12:123655988 | A | T | 2 | a0001c0002t0002g0012 a0001c0002t0028g0012 |
3 | HG00140.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.615+164A>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123655988 | |||||||
| chr12:123656068 | G | A | 1 | a0001c0001t0008g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.615+244G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656068 | |||||||
| chr12:123656332 | C | T | 2 | a0001c0003t0004g0041 a0001c0003t0004g0044 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.615+508C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656332 | |||||||
| chr12:123656482 | C | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(17): Show |
34 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.615+658C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656482 | |||||||
| chr12:123656589 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0012g0039 |
2 | HG02970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.615+765G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656589 | |||||||
| chr12:123656723 | C | T | 2 | a0001c0003t0004g0041 a0001c0003t0004g0044 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.615+899C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656723 | |||||||
| chr12:123656765 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.615+941A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656765 | |||||||
| chr12:123656787 | G | C | 9 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0079 others(6): Show |
11 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.615+963G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656787 | |||||||
| chr12:123656815 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(96): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.615+991A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656815 | |||||||
| chr12:123656836 | C | T | 25 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(22): Show |
26 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.615+1012C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656836 | |||||||
| chr12:123656935 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.615+1111A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656935 | |||||||
| chr12:123656941 | A | C | 4 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0162 others(1): Show |
6 | HG01243.hp2 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1117A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656941 | |||||||
| chr12:123656971 | T | G | 3 | a0001c0002t0003g0016 a0001c0002t0003g0118 a0001c0002t0003g0158 |
5 | HG01243.hp1 HG02818.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+1147T>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123656971 | |||||||
| chr12:123657115 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(16): Show |
33 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1291C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657115 | |||||||
| chr12:123657173 | CT | C | 6 | a0001c0001t0001g0105 a0001c0002t0012g0038 a0001c0002t0012g0039 others(3): Show |
6 | HG02897.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.615+1361delT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 123657173 | ||||||
| chr12:123657202 | A | G | 39 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(36): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.615+1378A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657202 | |||||||
| chr12:123657210 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.615+1386T>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657210 | |||||||
| chr12:123657385 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.615+1561G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657385 | |||||||
| chr12:123657389 | G | A | 1 | a0001c0002t0012g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.615+1565G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657389 | |||||||
| chr12:123657482 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.615+1658G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657482 | |||||||
| chr12:123657520 | G | A | 2 | a0001c0002t0003g0149 a0001c0002t0013g0151 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.615+1696G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657520 | |||||||
| chr12:123657550 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.615+1726A>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657550 | |||||||
| chr12:123657748 | T | A | 10 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(7): Show |
15 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.616-1768T>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657748 | |||||||
| chr12:123657838 | G | T | 1 | a0001c0002t0018g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.616-1678G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123657838 | |||||||
| chr12:123658044 | A | G | 39 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0008 others(36): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.616-1472A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658044 | |||||||
| chr12:123658158 | A | G | 9 | a0001c0003t0004g0017 a0001c0003t0004g0041 a0001c0003t0004g0042 others(6): Show |
10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-1358A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658158 | |||||||
| chr12:123658179 | C | G | 20 | a0001c0002t0003g0010 a0001c0002t0003g0016 a0001c0002t0003g0118 others(17): Show |
27 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.616-1337C>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658179 | |||||||
| chr12:123658463 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03710.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.616-1053G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658463 | |||||||
| chr12:123658485 | G | A | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.616-1031G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658485 | |||||||
| chr12:123658491 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.616-1025G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658491 | |||||||
| chr12:123658746 | G | A | 4 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0162 others(1): Show |
6 | HG01243.hp2 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-770G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658746 | |||||||
| chr12:123658826 | A | G | 1 | a0001c0002t0012g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.616-690A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658826 | |||||||
| chr12:123658999 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0033 others(17): Show |
34 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.616-517A>G | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123658999 | |||||||
| chr12:123659195 | C | T | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.616-321C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123659195 | |||||||
| chr12:123659400 | G | T | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.616-116G>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123659400 | |||||||
| chr12:123659405 | G | A | 1 | a0001c0003t0004g0159 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.616-111G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 9/12 | chr12 | 123659405 | |||||||
| chr12:123659603 | C | T | 21 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(18): Show |
22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.684+19C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 10/12 | chr12 | 123659603 | |||||||
| chr12:123659606 | C | T | 1 | a0001c0002t0026g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.684+22C>T | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 10/12 | chr12 | 123659606 | |||||||
| chr12:123659636 | G | A | 11 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(8): Show |
11 | HG01346.hp1 HG01975.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.684+52G>A | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 10/12 | chr12 | 123659636 | |||||||
| chr12:123659732 | G | C | 25 | a0001c0002t0005g0047 a0001c0002t0005g0048 a0001c0002t0005g0049 others(22): Show |
26 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.685-63G>C | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 10/12 | chr12 | 123659732 | |||||||
| chr12:123660025 | CT | C | 17 | a0001c0002t0002g0059 a0001c0002t0003g0010 a0001c0002t0003g0016 others(14): Show |
22 | HG01243.hp1 HG01516.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.821-10delT | GTF2H3 | ENSG00000111358.14 | transcript | ENST00000543341.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 123660025 |