Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5612 |
| ensemblid | ENSG00000137492.9 |
| hgncid | 9440 |
| symbol | THAP12 |
| name | THAP domain containing 12 |
| refseq_nuc | NM_004705.4 |
| refseq_prot | NP_004696.2 |
| ensembl_nuc | ENST00000260045.8 |
| ensembl_prot | ENSP00000260045.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 76349956 |
| end | 76381132 |
| strand | - |
| ver | v1.2 |
| region | chr11:76349956-76381132 |
| region5000 | chr11:76344956-76386132 |
| regionname0 | THAP12_chr11_76349956_76381132 |
| regionname5000 | THAP12_chr11_76344956_76386132 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 761 | 354 | 75 | 65 | 155 | 13 | 44 | 119 | THAP12_chr11_76344956_76386132 | THAP12 | MPNFC others(756): Show |
chr11 | 76344956 | 76386132 |
| a0002 | 0/0 | 761 | 26 | 0 | 3 | 22 | 1 | 0 | 17 | THAP12_chr11_76344956_76386132 | THAP12 | MPNFC others(756): Show |
chr11 | 76344956 | 76386132 |
| a0003 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | MPNFC others(756): Show |
chr11 | 76344956 | 76386132 |
| a0004 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | MPNFC others(756): Show |
chr11 | 76344956 | 76386132 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2283 | 350 | 71 | 65 | 155 | 13 | 44 | THAP12_chr11_76344956_76386132 | THAP12 | ATGCC others(2278): Show |
chr11 | 76344956 | 76386132 | ||
| a0001c0003 | 0/0 | 2283 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | ATGCC others(2278): Show |
chr11 | 76344956 | 76386132 | ||
| a0002c0002 | 0/0 | 2283 | 26 | 0 | 3 | 22 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | ATGCC others(2278): Show |
chr11 | 76344956 | 76386132 | ||
| a0003c0004 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | ATGCC others(2278): Show |
chr11 | 76344956 | 76386132 | ||
| a0004c0005 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | ATGCC others(2278): Show |
chr11 | 76344956 | 76386132 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3490 | 334 | 60 | 65 | 151 | 13 | 43 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0001t0002 | 0/0 | 3490 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0001t0003 | 0/0 | 3490 | 4 | 0 | 0 | 4 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0001t0004 | 0/0 | 3490 | 3 | 3 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0001t0005 | 0/0 | 3490 | 3 | 3 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0001t0007 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0001t0008 | 0/0 | 3490 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0001c0003t0001 | 0/0 | 3490 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0002c0002t0001 | 0/0 | 3490 | 24 | 0 | 3 | 20 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0002c0002t0006 | 0/0 | 3490 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0003c0004t0001 | 0/0 | 3490 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| a0004c0005t0001 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | GCATT others(3485): Show |
chr11 | 76344956 | 76386132 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 2 | 4 | 2 | 2 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0003 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0004 | 0/0 | 8 | 6 | 0 | 1 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0006 | 0/0 | 6 | 2 | 1 | 1 | 0 | 2 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0002c0002t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| a0004c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0046 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00558 | hp2 | a0002 | c0002 | t0006 | g0019 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02071 | hp1 | a0002 | c0002 | t0006 | g0019 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02080 | hp1 | a0003 | c0004 | t0001 | g0042 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0280 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03209 | hp2 | a0004 | c0005 | t0001 | g0057 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0239 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | GIH | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | GIH | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0107 | REF | REF | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76351745 | C | G | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1405G>C | p.Val469Leu | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 1701/3490 | 1405/2286 | 469/761 | chr11 | 76351745 | |||
| chr11:76352087 | T | C | 1 | a0002 | 26 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(23): Show |
missense_variant | MODERATE | c.1063A>G | p.Ile355Val | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 1359/3490 | 1063/2286 | 355/761 | chr11 | 76352087 | |||
| chr11:76380805 | G | T | 1 | a0003 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.32C>A | p.Thr11Lys | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/5 | 328/3490 | 32/2286 | 11/761 | chr11 | 76380805 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76352082 | G | A | 2 | a0001c0003 a0004c0005 |
5 | HG02559.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
synonymous_variant | LOW | c.1068C>T | p.Tyr356Tyr | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 1364/3490 | 1068/2286 | 356/761 | chr11 | 76352082 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76350241 | G | A | 1 | a0001c0001t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 623 | chr11 | 76350241 | ||||||
| chr11:76350368 | G | A | 3 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*496C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 496 | chr11 | 76350368 | ||||||
| chr11:76350639 | G | A | 1 | a0001c0001t0003 | 4 | NA18947.hp2 NA18955.hp2 NA18968.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 225 | chr11 | 76350639 | ||||||
| chr11:76350703 | A | G | 1 | a0001c0001t0002 | 4 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*161T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 161 | chr11 | 76350703 | ||||||
| chr11:76350782 | T | G | 1 | a0002c0002t0006 | 2 | HG00558.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*82A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 82 | chr11 | 76350782 | ||||||
| chr11:76380917 | G | A | 1 | a0001c0001t0008 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/5 | 81 | chr11 | 76380917 | ||||||
| chr11:76381027 | G | A | 1 | a0001c0001t0005 | 3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-191C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/5 | 191 | chr11 | 76381027 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76352827 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0119 |
3 | NA18969.hp2 NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.356-33G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76352827 | |||||||
| chr11:76352843 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.356-49G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76352843 | |||||||
| chr11:76353073 | C | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
348 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.356-279G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353073 | |||||||
| chr11:76353222 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.356-428A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353222 | |||||||
| chr11:76353574 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.356-780A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353574 | |||||||
| chr11:76353869 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG00544.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.356-1075G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353869 | |||||||
| chr11:76353870 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.356-1076C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353870 | |||||||
| chr11:76353922 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.356-1128A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353922 | |||||||
| chr11:76353964 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.356-1170C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353964 | |||||||
| chr11:76354003 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(55): Show |
86 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.356-1209G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354003 | |||||||
| chr11:76354018 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.356-1224T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354018 | |||||||
| chr11:76354023 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.356-1229G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354023 | |||||||
| chr11:76354148 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(88): Show |
117 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.356-1354A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354148 | |||||||
| chr11:76354163 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.356-1369C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354163 | |||||||
| chr11:76354197 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.356-1403G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354197 | |||||||
| chr11:76354318 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0183 |
3 | HG01243.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.355+1300A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354318 | |||||||
| chr11:76354321 | T | C | 1 | a0001c0001t0001g0027 | 2 | NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.355+1297A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354321 | |||||||
| chr11:76354380 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.355+1238C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354380 | |||||||
| chr11:76354540 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.355+1078A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354540 | |||||||
| chr11:76354749 | G | A | 16 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0016 others(13): Show |
26 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.355+869C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354749 | |||||||
| chr11:76354770 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.355+848T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354770 | |||||||
| chr11:76354927 | A | G | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.355+691T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354927 | |||||||
| chr11:76354981 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+637C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354981 | |||||||
| chr11:76355092 | G | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.355+526C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76355092 | |||||||
| chr11:76355666 | G | GA | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-13dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76355666 | |||||||
| chr11:76355706 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.319-52G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76355706 | |||||||
| chr11:76356111 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.319-457T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356111 | |||||||
| chr11:76356112 | A | AAG | 34 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(31): Show |
44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.319-460_319-459dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356112 | |||||||
| chr11:76356256 | C | CT | 34 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(31): Show |
44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.319-603_319-602ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356256 | |||||||
| chr11:76356337 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.319-683A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356337 | |||||||
| chr11:76356388 | C | T | 1 | a0002c0002t0001g0050 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.319-734G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356388 | |||||||
| chr11:76356398 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | NA18612.hp1 NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.319-744G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356398 | |||||||
| chr11:76356528 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.319-874C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356528 | |||||||
| chr11:76356551 | A | G | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.319-897T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356551 | |||||||
| chr11:76356583 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-929C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356583 | |||||||
| chr11:76356780 | C | T | 3 | a0002c0002t0001g0049 a0002c0002t0001g0051 a0002c0002t0001g0058 |
3 | NA18940.hp2 NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.319-1126G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356780 | |||||||
| chr11:76356937 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.319-1283C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356937 | |||||||
| chr11:76357423 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(56): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.319-1769A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357423 | |||||||
| chr11:76357510 | ATT | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.319-1858_319-1857d others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357510 | |||||||
| chr11:76357536 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(87): Show |
116 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.319-1882G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357536 | |||||||
| chr11:76357812 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0079 |
2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.319-2158G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357812 | |||||||
| chr11:76357921 | CA | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0231 a0001c0001t0001g0256 others(3): Show |
7 | HG01261.hp2 HG01358.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-2268delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357921 | |||||||
| chr11:76357936 | C | T | 6 | a0001c0001t0001g0227 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG00733.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-2282G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357936 | |||||||
| chr11:76358043 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.319-2389A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358043 | |||||||
| chr11:76358053 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0212 a0001c0001t0001g0235 others(2): Show |
6 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-2399G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358053 | |||||||
| chr11:76358164 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.319-2510T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358164 | |||||||
| chr11:76358195 | G | GA | 9 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(6): Show |
9 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-2542dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358195 | |||||||
| chr11:76358195 | GA | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(56): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.319-2542delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358195 | |||||||
| chr11:76358205 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.319-2551T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358205 | |||||||
| chr11:76358233 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.319-2579G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358233 | |||||||
| chr11:76358327 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.318+2629A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358327 | |||||||
| chr11:76358362 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.318+2594A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358362 | |||||||
| chr11:76358479 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+2477A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358479 | |||||||
| chr11:76358561 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+2395A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358561 | |||||||
| chr11:76358620 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0165 |
3 | HG01175.hp1 HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.318+2336G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358620 | |||||||
| chr11:76358817 | C | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+2139G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358817 | |||||||
| chr11:76358934 | A | T | 1 | a0001c0001t0004g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.318+2022T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358934 | |||||||
| chr11:76358971 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG01109.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.318+1985T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358971 | |||||||
| chr11:76359038 | G | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+1918C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359038 | |||||||
| chr11:76359314 | T | C | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+1642A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359314 | |||||||
| chr11:76359375 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0250 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.318+1581A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359375 | |||||||
| chr11:76359409 | G | A | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.318+1547C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359409 | |||||||
| chr11:76359555 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.318+1401G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359555 | |||||||
| chr11:76359576 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(26): Show |
46 | HG00609.hp2 HG00642.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.318+1380G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359576 | |||||||
| chr11:76359654 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.318+1302G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359654 | |||||||
| chr11:76359758 | T | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0276 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.318+1198A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359758 | |||||||
| chr11:76359831 | G | GA | 34 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(31): Show |
44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.318+1124dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359831 | |||||||
| chr11:76359832 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+1124T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359832 | |||||||
| chr11:76359878 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0216 a0001c0001t0001g0222 others(2): Show |
7 | HG01074.hp2 HG01081.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1078T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359878 | |||||||
| chr11:76359967 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0259 |
2 | HG00673.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.318+989T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359967 | |||||||
| chr11:76360029 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.318+927C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360029 | |||||||
| chr11:76360060 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+896T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360060 | |||||||
| chr11:76360090 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(56): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.318+866A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360090 | |||||||
| chr11:76360171 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.318+785A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360171 | |||||||
| chr11:76360248 | C | T | 3 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 |
3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.318+708G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360248 | |||||||
| chr11:76360249 | A | G | 1 | a0002c0002t0001g0047 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.318+707T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360249 | |||||||
| chr11:76360323 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.318+633T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360323 | |||||||
| chr11:76360328 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.318+628A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360328 | |||||||
| chr11:76360428 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.318+528C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360428 | |||||||
| chr11:76360691 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.318+265C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360691 | |||||||
| chr11:76361498 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.211-435C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76361498 | |||||||
| chr11:76361749 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.211-686A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76361749 | |||||||
| chr11:76362352 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0089 others(1): Show |
4 | NA18949.hp2 NA19000.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1289C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362352 | |||||||
| chr11:76362387 | A | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.211-1324T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362387 | |||||||
| chr11:76362541 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.211-1478C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362541 | |||||||
| chr11:76362795 | G | C | 1 | a0001c0001t0004g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211-1732C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362795 | |||||||
| chr11:76362828 | G | GA | 4 | a0001c0001t0002g0097 a0001c0001t0004g0092 a0001c0001t0004g0093 others(1): Show |
4 | HG02622.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1766dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362828 | |||||||
| chr11:76362998 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.211-1935G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362998 | |||||||
| chr11:76363013 | T | C | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1950A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363013 | |||||||
| chr11:76363048 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.211-1985C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363048 | |||||||
| chr11:76363056 | T | C | 22 | a0001c0001t0001g0204 a0001c0003t0001g0045 a0001c0003t0001g0052 others(19): Show |
32 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.211-1993A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363056 | |||||||
| chr11:76363072 | G | C | 1 | a0001c0001t0007g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211-2009C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363072 | |||||||
| chr11:76363076 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.211-2013C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363076 | |||||||
| chr11:76363149 | A | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(127): Show |
167 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.211-2086T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363149 | |||||||
| chr11:76363473 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.210+2379T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363473 | |||||||
| chr11:76363496 | A | C | 1 | a0001c0003t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.210+2356T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363496 | |||||||
| chr11:76363558 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.210+2294A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363558 | |||||||
| chr11:76363562 | G | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0150 |
4 | NA18947.hp2 NA18955.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+2290C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363562 | |||||||
| chr11:76363571 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.210+2281T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363571 | |||||||
| chr11:76363572 | T | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.210+2280A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363572 | |||||||
| chr11:76363589 | T | TTTTG | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
233 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.210+2259_210+2262d others(6): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363589 | |||||||
| chr11:76363589 | T | TTTTGTTT others(1): Show |
89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(86): Show |
115 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.210+2255_210+2262d others(10): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363589 | |||||||
| chr11:76363625 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+2227C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363625 | |||||||
| chr11:76363757 | T | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(93): Show |
123 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.210+2095A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363757 | |||||||
| chr11:76363760 | T | G | 1 | a0001c0001t0001g0072 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.210+2092A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363760 | |||||||
| chr11:76363845 | A | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+2007T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363845 | |||||||
| chr11:76363848 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+2004A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363848 | |||||||
| chr11:76363851 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.210+2001G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363851 | |||||||
| chr11:76363970 | C | G | 13 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(10): Show |
13 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.210+1882G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363970 | |||||||
| chr11:76364064 | A | G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(32): Show |
44 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.210+1788T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364064 | |||||||
| chr11:76364065 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01099.hp2 HG01346.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+1787A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364065 | |||||||
| chr11:76364099 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.210+1753C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364099 | |||||||
| chr11:76364629 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.210+1223G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364629 | |||||||
| chr11:76364691 | T | C | 1 | a0001c0001t0005g0282 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.210+1161A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364691 | |||||||
| chr11:76365141 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.210+711G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365141 | |||||||
| chr11:76365142 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.210+710C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365142 | |||||||
| chr11:76365251 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.210+601C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365251 | |||||||
| chr11:76365292 | T | TA | 26 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0101 others(23): Show |
38 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.210+559dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365292 | |||||||
| chr11:76365292 | TA | T | 15 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0118 others(12): Show |
15 | HG00323.hp1 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.210+559delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365292 | |||||||
| chr11:76365293 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.210+559T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365293 | |||||||
| chr11:76365356 | A | AGTTTT | 6 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0139 others(3): Show |
11 | HG00733.hp2 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+491_210+495dup others(5): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365356 | |||||||
| chr11:76365394 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.210+458A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365394 | |||||||
| chr11:76365407 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210+445G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365407 | |||||||
| chr11:76365496 | A | G | 3 | a0002c0002t0001g0013 a0002c0002t0001g0047 a0002c0002t0001g0048 |
5 | NA18955.hp1 NA18992.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+356T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365496 | |||||||
| chr11:76365515 | C | T | 5 | a0001c0001t0001g0227 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG00733.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+337G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365515 | |||||||
| chr11:76365573 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210+279C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365573 | |||||||
| chr11:76365736 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.210+116C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365736 | |||||||
| chr11:76365749 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+103C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365749 | |||||||
| chr11:76365798 | T | TGA | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+52_210+53dupTC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365798 | |||||||
| chr11:76366100 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-128C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366100 | |||||||
| chr11:76366276 | A | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(57): Show |
88 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.90-304T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366276 | |||||||
| chr11:76366457 | A | G | 34 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(31): Show |
44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.90-485T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366457 | |||||||
| chr11:76366573 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.90-601G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366573 | |||||||
| chr11:76366629 | C | T | 35 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(32): Show |
44 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.90-657G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366629 | |||||||
| chr11:76366675 | C | T | 1 | a0001c0001t0004g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.90-703G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366675 | |||||||
| chr11:76366682 | G | GA | 8 | a0001c0001t0001g0114 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01261.hp2 HG02055.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.90-711dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366682 | |||||||
| chr11:76367081 | C | CT | 7 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0112 others(4): Show |
7 | HG00597.hp2 NA18948.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.90-1110dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367081 | |||||||
| chr11:76367081 | C | CTT | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.90-1111_90-1110dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367081 | |||||||
| chr11:76367085 | T | C | 3 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 |
3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.90-1113A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367085 | |||||||
| chr11:76367234 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-1262C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367234 | |||||||
| chr11:76367303 | C | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-1331G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367303 | |||||||
| chr11:76367563 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(127): Show |
167 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.90-1591A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367563 | |||||||
| chr11:76367595 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.90-1623C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367595 | |||||||
| chr11:76367715 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.90-1743C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367715 | |||||||
| chr11:76367820 | C | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(55): Show |
86 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.90-1848G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367820 | |||||||
| chr11:76367965 | TAC | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-1995_90-1994del others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367965 | |||||||
| chr11:76367994 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0171 |
2 | NA18987.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.90-2022A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367994 | |||||||
| chr11:76368112 | G | C | 10 | a0002c0002t0001g0013 a0002c0002t0001g0016 a0002c0002t0001g0017 others(7): Show |
14 | HG00323.hp2 NA18940.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.90-2140C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368112 | |||||||
| chr11:76368136 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.90-2164G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368136 | |||||||
| chr11:76368237 | A | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
348 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.90-2265T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368237 | |||||||
| chr11:76368300 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.90-2328A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368300 | |||||||
| chr11:76368674 | C | A | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-2702G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368674 | |||||||
| chr11:76368728 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.90-2756G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368728 | |||||||
| chr11:76369022 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(93): Show |
123 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.90-3050T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369022 | |||||||
| chr11:76369090 | G | C | 2 | a0001c0001t0001g0163 a0003c0004t0001g0042 |
2 | HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.90-3118C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369090 | |||||||
| chr11:76369162 | T | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(32): Show |
44 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.90-3190A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369162 | |||||||
| chr11:76369211 | A | T | 8 | a0001c0001t0001g0037 a0001c0001t0001g0204 a0001c0001t0001g0210 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-3239T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369211 | |||||||
| chr11:76369232 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.90-3260C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369232 | |||||||
| chr11:76369486 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.90-3514C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369486 | |||||||
| chr11:76369604 | A | G | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3632T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369604 | |||||||
| chr11:76369630 | A | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3658T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369630 | |||||||
| chr11:76369631 | GC | G | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3660delG | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369631 | |||||||
| chr11:76369634 | C | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3662G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369634 | |||||||
| chr11:76369635 | A | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3663T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369635 | |||||||
| chr11:76369636 | C | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3664G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369636 | |||||||
| chr11:76369637 | C | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3665G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369637 | |||||||
| chr11:76369699 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.90-3727C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369699 | |||||||
| chr11:76369846 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.90-3874C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369846 | |||||||
| chr11:76369922 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0151 |
3 | HG02602.hp1 HG02735.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.90-3950T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369922 | |||||||
| chr11:76370050 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0068 a0001c0001t0001g0074 others(1): Show |
5 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-4078C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370050 | |||||||
| chr11:76370151 | C | T | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-4179G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370151 | |||||||
| chr11:76370203 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-4231T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370203 | |||||||
| chr11:76370353 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-4381C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370353 | |||||||
| chr11:76370358 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.90-4386A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370358 | |||||||
| chr11:76370358 | TG | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(54): Show |
85 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.90-4387delC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370358 | |||||||
| chr11:76370359 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0173 |
2 | NA18966.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.90-4387C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370359 | |||||||
| chr11:76370365 | T | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0173 |
2 | NA18966.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.90-4393A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370365 | |||||||
| chr11:76370369 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0173 |
2 | NA18966.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.90-4397C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370369 | |||||||
| chr11:76370746 | C | T | 1 | a0001c0003t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.90-4774G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370746 | |||||||
| chr11:76370830 | G | GA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(100): Show |
145 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.90-4859dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370830 | |||||||
| chr11:76370835 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.90-4863T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370835 | |||||||
| chr11:76370841 | A | AAT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(38): Show |
70 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.90-4870_90-4869ins others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | |||||||
| chr11:76370841 | A | AATAT | 10 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0137 others(7): Show |
10 | HG01175.hp1 HG01978.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-4870_90-4869ins others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | |||||||
| chr11:76370841 | A | AT | 8 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG00323.hp1 HG01069.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-4870_90-4869ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | |||||||
| chr11:76370841 | A | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0128 a0001c0001t0001g0151 others(1): Show |
5 | HG02602.hp1 HG03516.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-4869T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | |||||||
| chr11:76370843 | A | AAT | 14 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0082 others(11): Show |
14 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.90-4873_90-4872dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370843 | |||||||
| chr11:76370843 | A | AT | 24 | a0001c0001t0001g0041 a0001c0001t0001g0078 a0001c0001t0001g0155 others(21): Show |
28 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.90-4872_90-4871ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370843 | |||||||
| chr11:76370843 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
132 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.90-4871T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370843 | |||||||
| chr11:76370845 | T | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0240 |
2 | HG01192.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.90-4873A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370845 | |||||||
| chr11:76370879 | A | G | 2 | a0002c0002t0001g0018 a0002c0002t0006g0019 |
4 | HG00558.hp2 HG02071.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-4907T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370879 | |||||||
| chr11:76370883 | G | A | 2 | a0002c0002t0001g0018 a0002c0002t0006g0019 |
4 | HG00558.hp2 HG02071.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-4911C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370883 | |||||||
| chr11:76370884 | T | TATTC | 19 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(16): Show |
27 | HG00323.hp2 HG00544.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.90-4916_90-4913dup others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370884 | |||||||
| chr11:76370884 | T | TTC | 2 | a0002c0002t0001g0018 a0002c0002t0006g0019 |
4 | HG00558.hp2 HG02071.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-4913_90-4912ins others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370884 | |||||||
| chr11:76370997 | G | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-5025C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370997 | |||||||
| chr11:76371018 | A | G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01099.hp2 HG01346.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-5046T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371018 | |||||||
| chr11:76371096 | C | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.90-5124G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371096 | |||||||
| chr11:76371233 | T | C | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-5261A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371233 | |||||||
| chr11:76371298 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
17 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.90-5326C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371298 | |||||||
| chr11:76371311 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0139 others(4): Show |
12 | HG00733.hp2 HG00735.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-5339G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371311 | |||||||
| chr11:76371336 | T | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0204 a0001c0001t0001g0210 others(7): Show |
11 | HG00639.hp1 HG01074.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.90-5364A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371336 | |||||||
| chr11:76371461 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG02056.hp1 NA18952.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.90-5489A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371461 | |||||||
| chr11:76371661 | CTTG | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-5692_90-5690del others(3): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371661 | |||||||
| chr11:76371688 | CCAAGGAG others(1): Show |
C | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-5724_90-5717del others(8): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371688 | |||||||
| chr11:76371710 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.90-5738G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371710 | |||||||
| chr11:76371810 | CT | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.90-5839delA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371810 | |||||||
| chr11:76371895 | C | T | 10 | a0002c0002t0001g0013 a0002c0002t0001g0016 a0002c0002t0001g0017 others(7): Show |
14 | HG00323.hp2 NA18940.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.90-5923G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371895 | |||||||
| chr11:76371919 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.90-5947A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371919 | |||||||
| chr11:76372091 | G | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(56): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90-6119C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372091 | |||||||
| chr11:76372205 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
346 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(343): Show |
intron_variant | MODIFIER | c.90-6233T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372205 | |||||||
| chr11:76372275 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.90-6303G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372275 | |||||||
| chr11:76372389 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0131 |
2 | HG02135.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.90-6417A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372389 | |||||||
| chr11:76372407 | T | TA | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
343 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.90-6436dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372407 | |||||||
| chr11:76372449 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.90-6477C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372449 | |||||||
| chr11:76372527 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(127): Show |
167 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.90-6555T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372527 | |||||||
| chr11:76372588 | T | TA | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-6617_90-6616ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372588 | |||||||
| chr11:76372589 | T | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-6617A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372589 | |||||||
| chr11:76372589 | TA | T | 24 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0063 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.90-6618delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372589 | |||||||
| chr11:76372656 | C | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0212 a0001c0001t0001g0235 others(2): Show |
6 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-6684G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372656 | |||||||
| chr11:76372701 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.90-6729A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372701 | |||||||
| chr11:76372774 | C | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(56): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90-6802G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372774 | |||||||
| chr11:76372887 | C | CA | 7 | a0001c0001t0001g0038 a0001c0001t0001g0205 a0001c0001t0001g0231 others(4): Show |
8 | HG01261.hp2 HG01358.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-6916dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372887 | |||||||
| chr11:76373147 | TCCAGCCT others(364): Show |
T | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.89+7230_90-7176del | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373147 | |||||||
| chr11:76373191 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
372 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(369): Show |
intron_variant | MODIFIER | c.90-7219A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373191 | |||||||
| chr11:76373217 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-7245C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373217 | |||||||
| chr11:76373343 | C | CA | 11 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(8): Show |
12 | HG00642.hp2 HG00673.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-7372dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373343 | |||||||
| chr11:76373371 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.89+7377A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373371 | |||||||
| chr11:76373380 | T | C | 1 | a0001c0001t0004g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89+7368A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373380 | |||||||
| chr11:76373489 | G | A | 1 | a0001c0003t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89+7259C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373489 | |||||||
| chr11:76373650 | T | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
348 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.89+7098A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373650 | |||||||
| chr11:76373718 | C | CA | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.89+7029dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373718 | |||||||
| chr11:76373775 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.89+6973G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373775 | |||||||
| chr11:76373873 | A | T | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.89+6875T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373873 | |||||||
| chr11:76374141 | A | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.89+6607T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374141 | |||||||
| chr11:76374215 | C | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
348 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.89+6533G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374215 | |||||||
| chr11:76374386 | C | CA | 9 | a0001c0001t0001g0041 a0001c0001t0001g0122 a0001c0001t0001g0131 others(6): Show |
10 | HG02080.hp2 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.89+6361dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374386 | |||||||
| chr11:76374386 | CA | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(65): Show |
93 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.89+6361delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374386 | |||||||
| chr11:76374386 | CAA | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(112): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.89+6360_89+6361del others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374386 | |||||||
| chr11:76374622 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.89+6126G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374622 | |||||||
| chr11:76374636 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+6112C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374636 | |||||||
| chr11:76374683 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.89+6065T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374683 | |||||||
| chr11:76374752 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.89+5996A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374752 | |||||||
| chr11:76374798 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+5950C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374798 | |||||||
| chr11:76374812 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.89+5936A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374812 | |||||||
| chr11:76374892 | C | CT | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+5855dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374892 | |||||||
| chr11:76375061 | G | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0250 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.89+5687C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375061 | |||||||
| chr11:76375070 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.89+5678A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375070 | |||||||
| chr11:76375169 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.89+5579A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375169 | |||||||
| chr11:76375235 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.89+5513T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375235 | |||||||
| chr11:76375390 | C | CT | 18 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0089 others(15): Show |
18 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.89+5357dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375390 | |||||||
| chr11:76375393 | T | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG00408.hp2 HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.89+5355A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375393 | |||||||
| chr11:76375747 | T | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0175 others(1): Show |
5 | HG00621.hp2 HG02080.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+5001A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | |||||||
| chr11:76375747 | T | TG | 34 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
48 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.89+5000dupC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | |||||||
| chr11:76375747 | T | TGG | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(87): Show |
128 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.89+4999_89+5000dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | |||||||
| chr11:76375747 | T | TGGG | 74 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.89+4998_89+5000dup others(3): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | |||||||
| chr11:76375747 | T | TGGGG | 20 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0089 others(17): Show |
22 | HG00733.hp1 HG01123.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.89+4997_89+5000dup others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | |||||||
| chr11:76375747 | TG | T | 27 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(24): Show |
37 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.89+5000delC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | |||||||
| chr11:76375756 | G | GT | 2 | a0001c0001t0001g0022 a0001c0001t0001g0103 |
3 | NA18988.hp1 NA19070.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.89+4991_89+4992ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375756 | |||||||
| chr11:76375994 | T | C | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+4754A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375994 | |||||||
| chr11:76376187 | G | A | 3 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG02622.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89+4561C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376187 | |||||||
| chr11:76376322 | A | T | 1 | a0001c0001t0004g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89+4426T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376322 | |||||||
| chr11:76376355 | T | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(60): Show |
90 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.89+4393A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376355 | |||||||
| chr11:76376456 | A | T | 1 | a0001c0001t0004g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.89+4292T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376456 | |||||||
| chr11:76376498 | G | C | 1 | a0001c0001t0004g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89+4250C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376498 | |||||||
| chr11:76376615 | G | GT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0197 a0001c0001t0001g0255 others(7): Show |
15 | HG01261.hp2 HG01358.hp1 HG03453.hp1 others(12): Show |
intron_variant | MODIFIER | c.89+4132dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376615 | |||||||
| chr11:76376615 | G | GTT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0015 others(56): Show |
79 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.89+4131_89+4132dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376615 | |||||||
| chr11:76376615 | G | GTTT | 19 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0199 others(16): Show |
20 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.89+4130_89+4132dup others(3): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376615 | |||||||
| chr11:76376623 | TG | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(10): Show |
20 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.89+4124delC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376623 | |||||||
| chr11:76376624 | G | GT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0027 others(10): Show |
13 | HG02055.hp1 HG02080.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.89+4123dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376624 | |||||||
| chr11:76376624 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(89): Show |
118 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.89+4124C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376624 | |||||||
| chr11:76376624 | GT | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(44): Show |
58 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.89+4123delA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376624 | |||||||
| chr11:76376711 | G | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.89+4037C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376711 | |||||||
| chr11:76376748 | T | TCTAAACA others(319): Show |
2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.89+3999_89+4000ins others(326): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376748 | |||||||
| chr11:76376748 | T | TCTAAACA others(320): Show |
1 | a0001c0001t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.89+3999_89+4000ins others(327): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376748 | |||||||
| chr11:76376800 | C | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.89+3948G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376800 | |||||||
| chr11:76377044 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+3704G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377044 | |||||||
| chr11:76377183 | T | C | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+3565A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377183 | |||||||
| chr11:76377823 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.89+2925G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377823 | |||||||
| chr11:76377860 | G | A | 1 | a0002c0002t0001g0058 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.89+2888C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377860 | |||||||
| chr11:76377884 | C | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+2864G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377884 | |||||||
| chr11:76377939 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.89+2809G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377939 | |||||||
| chr11:76378198 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.89+2550G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378198 | |||||||
| chr11:76378252 | T | C | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+2496A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378252 | |||||||
| chr11:76378256 | TA | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+2491delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378256 | |||||||
| chr11:76378406 | C | G | 3 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 |
3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.89+2342G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378406 | |||||||
| chr11:76378510 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.89+2238T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378510 | |||||||
| chr11:76378598 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.89+2150G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378598 | |||||||
| chr11:76378724 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(88): Show |
117 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.89+2024C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378724 | |||||||
| chr11:76378839 | C | T | 3 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG02622.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89+1909G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378839 | |||||||
| chr11:76379026 | T | A | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | NA18612.hp2 NA18966.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+1722A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379026 | |||||||
| chr11:76379041 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | NA18612.hp1 NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.89+1707C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379041 | |||||||
| chr11:76379130 | T | C | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.89+1618A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379130 | |||||||
| chr11:76379195 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.89+1553T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379195 | |||||||
| chr11:76379245 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.89+1503A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379245 | |||||||
| chr11:76379544 | G | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0271 a0001c0001t0001g0272 |
4 | NA18950.hp2 NA18982.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+1204C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379544 | |||||||
| chr11:76379618 | G | C | 1 | a0001c0001t0001g0041 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.89+1130C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379618 | |||||||
| chr11:76379645 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.89+1103A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379645 | |||||||
| chr11:76379799 | G | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.89+949C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379799 | |||||||
| chr11:76379894 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.89+854A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379894 | |||||||
| chr11:76379921 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.89+827A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379921 | |||||||
| chr11:76380049 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.89+699A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380049 | |||||||
| chr11:76380083 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.89+665C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380083 | |||||||
| chr11:76380245 | A | AT | 21 | a0001c0003t0001g0045 a0001c0003t0001g0052 a0001c0003t0001g0054 others(18): Show |
31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.89+502dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380245 | |||||||
| chr11:76380407 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.89+341G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380407 | |||||||
| chr11:76380444 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+304C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380444 | |||||||
| chr11:76380715 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.89+33C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380715 |