Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83591 |
| ensemblid | ENSG00000173451.7 |
| hgncid | 20854 |
| symbol | THAP2 |
| name | THAP domain containing 2 |
| refseq_nuc | NM_031435.4 |
| refseq_prot | NP_113623.1 |
| ensembl_nuc | ENST00000308086.3 |
| ensembl_prot | ENSP00000310796.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 71664301 |
| end | 71680644 |
| strand | + |
| ver | v1.2 |
| region | chr12:71664301-71680644 |
| region5000 | chr12:71659301-71685644 |
| regionname0 | THAP2_chr12_71664301_71680644 |
| regionname5000 | THAP2_chr12_71659301_71685644 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 228 | 348 | 84 | 51 | 158 | 14 | 39 | 124 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(223): Show |
chr12 | 71659301 | 71685644 |
| a0002 | 0/0 | 227 | 10 | 0 | 3 | 2 | 0 | 5 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(222): Show |
chr12 | 71659301 | 71685644 |
| a0003 | 0/0 | 228 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(223): Show |
chr12 | 71659301 | 71685644 |
| a0004 | 0/0 | 228 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(223): Show |
chr12 | 71659301 | 71685644 |
| a0005 | 0/0 | 228 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(223): Show |
chr12 | 71659301 | 71685644 |
| a0006 | 0/0 | 228 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(223): Show |
chr12 | 71659301 | 71685644 |
| a0007 | 0/0 | 223 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | MPTKC others(218): Show |
chr12 | 71659301 | 71685644 |
| a0008 | 0/0 | 181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | MPTNC others(176): Show |
chr12 | 71659301 | 71685644 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 684 | 346 | 83 | 50 | 158 | 14 | 39 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0001c0006 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0001c0007 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0002c0002 | 0/0 | 681 | 10 | 0 | 3 | 2 | 0 | 5 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(676): Show |
chr12 | 71659301 | 71685644 | ||
| a0003c0003 | 0/0 | 684 | 10 | 10 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0004c0004 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0005c0008 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0006c0010 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 | ||
| a0007c0005 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(664): Show |
chr12 | 71659301 | 71685644 | ||
| a0008c0009 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | ATGCC others(679): Show |
chr12 | 71659301 | 71685644 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4432 | 182 | 20 | 20 | 114 | 6 | 22 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0002 | 1/1 | 4432 | 89 | 8 | 24 | 35 | 7 | 13 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0003 | 0/0 | 4436 | 22 | 20 | 2 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4431): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0004 | 0/0 | 4433 | 11 | 10 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4428): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0005 | 0/0 | 4433 | 12 | 4 | 1 | 2 | 1 | 4 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4428): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0006 | 0/0 | 4431 | 8 | 8 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4426): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0007 | 0/0 | 4431 | 5 | 5 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4426): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0008 | 0/0 | 4436 | 4 | 3 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4431): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0009 | 0/0 | 4432 | 3 | 0 | 1 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0010 | 0/0 | 4432 | 2 | 2 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0011 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0013 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0014 | 0/0 | 4431 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4426): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0015 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0016 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0017 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0018 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0001t0020 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0001c0006t0004 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4428): Show |
chr12 | 71659301 | 71685644 |
| a0001c0007t0002 | 0/0 | 4432 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0002c0002t0003 | 0/0 | 4433 | 10 | 0 | 3 | 2 | 0 | 5 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4428): Show |
chr12 | 71659301 | 71685644 |
| a0003c0003t0001 | 0/0 | 4432 | 10 | 10 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0004c0004t0001 | 0/0 | 4432 | 2 | 0 | 0 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0005c0008t0001 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0006c0010t0019 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| a0007c0005t0012 | 0/0 | 4417 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4412): Show |
chr12 | 71659301 | 71685644 |
| a0008c0009t0002 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | AGTCG others(4427): Show |
chr12 | 71659301 | 71685644 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 51 | 4 | 5 | 39 | 0 | 3 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0003 | 0/0 | 52 | 3 | 2 | 41 | 0 | 6 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 0 | 5 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0002 | 1/0 | 63 | 5 | 20 | 23 | 4 | 10 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0004 | 0/0 | 10 | 8 | 2 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0004g0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0006 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0006g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0007g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0008g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0009g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0010g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0014g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0018g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0001t0020g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0006t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0001c0007t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0002c0002t0003g0007 | 0/0 | 8 | 0 | 2 | 2 | 0 | 4 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0003c0003t0001g0001 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0004c0004t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0005c0008t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0006c0010t0019g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0007c0005t0012g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| a0008c0009t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00741 | hp1 | a0002 | c0002 | t0003 | g0056 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01081 | hp1 | a0001 | c0007 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0025 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01975 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02071 | hp1 | a0005 | c0008 | t0001 | g0013 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02083 | hp1 | a0006 | c0010 | t0019 | g0063 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02135 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0092 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0050 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0074 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02965 | hp2 | a0001 | c0006 | t0004 | g0010 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0097 | AFR | GWD | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0066 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0007 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0062 | SAS | BEB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0007 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0007 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | YRI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18948 | hp1 | a0001 | c0001 | t0020 | g0070 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18967 | hp1 | a0001 | c0001 | t0014 | g0024 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18977 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18981 | hp2 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18988 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18992 | hp2 | a0007 | c0005 | t0012 | g0057 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | LWK | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | LWK | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | LWK | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | LWK | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19059 | hp1 | a0008 | c0009 | t0002 | g0044 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19063 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19081 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | YRI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0078 | AFR | ASW | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0006 | EUR | TSI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0007 | SAS | GIH | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | MSL | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | USA | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | USA | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA18955 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | LWK | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0037 | REF | REF | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | THAP2_chr12_71659301_71685644 | THAP2 | chr12 | 71659301 | 71685644 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71664521 | T | A | 1 | a0007 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.12T>A | p.Asn4Lys | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 221/4432 | 12/687 | 4/228 | chr12 | 71664521 | |||
| chr12:71664535 | GCTGTGCC others(8): Show |
G | 1 | a0007 | 1 | NA18992.hp2 | conservative_inframe_deletion | MODERATE | c.28_42delTGTGCCACTA others(5): Show |
p.Cys10_Tyr14del | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 237/4432 | 28/687 | 10/228 | INFO_REALIGN_3_PRIME | chr12 | 71664535 | ||
| chr12:71664564 | A | T | 1 | a0007 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.55A>T | p.Asn19Tyr | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 264/4432 | 55/687 | 19/228 | chr12 | 71664564 | |||
| chr12:71664577 | A | T | 1 | a0007 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.68A>T | p.His23Leu | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 277/4432 | 68/687 | 23/228 | chr12 | 71664577 | |||
| chr12:71664578 | C | A | 1 | a0007 | 1 | NA18992.hp2 | missense_variant&splice_region_variant | MODERATE | c.69C>A | p.His23Gln | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 278/4432 | 69/687 | 23/228 | chr12 | 71664578 | |||
| chr12:71674229 | A | G | 1 | a0006 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.98A>G | p.Lys33Arg | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/3 | 307/4432 | 98/687 | 33/228 | chr12 | 71674229 | |||
| chr12:71674231 | G | A | 1 | a0006 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.100G>A | p.Glu34Lys | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/3 | 309/4432 | 100/687 | 34/228 | chr12 | 71674231 | |||
| chr12:71676725 | AGTT | A | 1 | a0002 | 10 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
disruptive_inframe_deletion | MODERATE | c.308_310delGTT | p.Cys103del | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 517/4432 | 308/687 | 103/228 | INFO_REALIGN_3_PRIME | chr12 | 71676725 | ||
| chr12:71676776 | C | G | 1 | a0008 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.355C>G | p.Gln119Glu | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 564/4432 | 355/687 | 119/228 | chr12 | 71676776 | |||
| chr12:71676801 | C | A | 1 | a0008 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.380C>A | p.Ala127Asp | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 589/4432 | 380/687 | 127/228 | chr12 | 71676801 | |||
| chr12:71676930 | C | T | 1 | a0003 | 10 | HG02109.hp1 HG02280.hp2 HG02717.hp1 others(7): Show |
missense_variant | MODERATE | c.509C>T | p.Thr170Met | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 718/4432 | 509/687 | 170/228 | chr12 | 71676930 | |||
| chr12:71676962 | G | A | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.541G>A | p.Val181Ile | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 750/4432 | 541/687 | 181/228 | chr12 | 71676962 | |||
| chr12:71676966 | T | A | 1 | a0008 | 1 | NA19059.hp1 | stop_gained | HIGH | c.545T>A | p.Leu182* | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 754/4432 | 545/687 | 182/228 | chr12 | 71676966 | |||
| chr12:71676998 | A | G | 1 | a0004 | 2 | NA18988.hp2 NA19081.hp2 |
missense_variant | MODERATE | c.577A>G | p.Thr193Ala | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 786/4432 | 577/687 | 193/228 | chr12 | 71676998 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71664533 | G | A | 1 | a0001c0006 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.24G>A | p.Ala8Ala | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 233/4432 | 24/687 | 8/228 | chr12 | 71664533 | |||
| chr12:71664557 | G | A | 1 | a0001c0007 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.48G>A | p.Lys16Lys | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 257/4432 | 48/687 | 16/228 | chr12 | 71664557 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71664340 | T | A | 1 | a0001c0001t0011 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-170T>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 170 | chr12 | 71664340 | ||||||
| chr12:71664403 | C | T | 1 | a0001c0001t0020 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 107 | chr12 | 71664403 | ||||||
| chr12:71664425 | C | T | 1 | a0001c0001t0009 | 3 | HG01975.hp1 NA18979.hp1 NA19063.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-85C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | chr12 | 71664425 | |||||||
| chr12:71664484 | G | A | 1 | a0007c0005t0012 | 1 | NA18992.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 26 | chr12 | 71664484 | ||||||
| chr12:71664499 | G | A | 1 | a0007c0005t0012 | 1 | NA18992.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 11 | chr12 | 71664499 | ||||||
| chr12:71664500 | G | T | 1 | a0007c0005t0012 | 1 | NA18992.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10G>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/3 | 10 | chr12 | 71664500 | ||||||
| chr12:71677178 | T | G | 1 | a0001c0001t0013 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70T>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 70 | chr12 | 71677178 | ||||||
| chr12:71677235 | A | C | 1 | a0006c0010t0019 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 127 | chr12 | 71677235 | ||||||
| chr12:71677265 | A | G | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
281 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*157A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 157 | chr12 | 71677265 | ||||||
| chr12:71677380 | A | T | 1 | a0001c0001t0018 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 272 | chr12 | 71677380 | ||||||
| chr12:71677668 | T | TATTA | 3 | a0001c0001t0003 a0001c0001t0008 a0002c0002t0003 |
36 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*560_*561insATTA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 561 | chr12 | 71677668 | ||||||
| chr12:71677935 | G | GT | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0006t0004 |
24 | HG01109.hp2 HG01346.hp1 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*833dupT | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 834 | INFO_REALIGN_3_PRIME | chr12 | 71677935 | |||||
| chr12:71678252 | A | G | 1 | a0001c0001t0017 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 1144 | chr12 | 71678252 | ||||||
| chr12:71678365 | T | C | 1 | a0001c0001t0011 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 1257 | chr12 | 71678365 | ||||||
| chr12:71678474 | A | G | 1 | a0001c0001t0016 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 1366 | chr12 | 71678474 | ||||||
| chr12:71678669 | T | A | 2 | a0001c0001t0004 a0001c0006t0004 |
12 | HG01109.hp2 HG02572.hp2 HG02818.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1561T>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 1561 | chr12 | 71678669 | ||||||
| chr12:71678669 | TA | T | 3 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0014 |
14 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1566delA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 1566 | INFO_REALIGN_3_PRIME | chr12 | 71678669 | |||||
| chr12:71678689 | T | C | 1 | a0001c0001t0006 | 8 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1581T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 1581 | chr12 | 71678689 | ||||||
| chr12:71679211 | A | G | 1 | a0001c0001t0008 | 4 | HG01496.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2103A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 2103 | chr12 | 71679211 | ||||||
| chr12:71679989 | G | A | 1 | a0001c0001t0015 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2881G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 2881 | chr12 | 71679989 | ||||||
| chr12:71680411 | G | C | 1 | a0001c0001t0010 | 2 | HG02615.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3303G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 3/3 | 3303 | chr12 | 71680411 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71664636 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(63): Show |
220 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.71+56G>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71664636 | |||||||
| chr12:71664703 | A | T | 1 | a0007c0005t0012g0057 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.71+123A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71664703 | |||||||
| chr12:71664723 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71+143C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71664723 | |||||||
| chr12:71664725 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.71+145C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71664725 | |||||||
| chr12:71664751 | T | G | 2 | a0001c0001t0003g0022 a0001c0001t0003g0031 |
3 | HG02486.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.71+171T>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71664751 | |||||||
| chr12:71664812 | G | GT | 2 | a0002c0002t0003g0007 a0002c0002t0003g0056 |
9 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+233dupT | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71664812 | ||||||
| chr12:71664875 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.71+295C>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71664875 | |||||||
| chr12:71665018 | T | C | 2 | a0002c0002t0003g0007 a0002c0002t0003g0056 |
9 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+438T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665018 | |||||||
| chr12:71665269 | G | T | 4 | a0001c0001t0002g0055 a0001c0001t0004g0010 a0001c0001t0007g0010 others(1): Show |
8 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+689G>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665269 | |||||||
| chr12:71665346 | A | G | 1 | a0001c0001t0005g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71+766A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665346 | |||||||
| chr12:71665377 | C | T | 1 | a0001c0001t0010g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71+797C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665377 | |||||||
| chr12:71665389 | CCCTA | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0096 |
4 | HG01258.hp2 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+814_71+817delCC others(2): Show |
THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71665389 | ||||||
| chr12:71665397 | A | G | 1 | a0001c0001t0008g0025 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.71+817A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665397 | |||||||
| chr12:71665543 | A | G | 4 | a0001c0001t0002g0055 a0001c0001t0004g0010 a0001c0001t0007g0010 others(1): Show |
8 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+963A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665543 | |||||||
| chr12:71665725 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0005g0014 |
3 | NA18949.hp1 NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.71+1145T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665725 | |||||||
| chr12:71665769 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
259 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.71+1189A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665769 | |||||||
| chr12:71665774 | G | A | 2 | a0002c0002t0003g0007 a0002c0002t0003g0056 |
9 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+1194G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665774 | |||||||
| chr12:71665919 | T | C | 2 | a0002c0002t0003g0007 a0002c0002t0003g0056 |
9 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+1339T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665919 | |||||||
| chr12:71665975 | T | C | 4 | a0001c0001t0002g0055 a0001c0001t0004g0010 a0001c0001t0007g0010 others(1): Show |
8 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+1395T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665975 | |||||||
| chr12:71665986 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+1406C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71665986 | |||||||
| chr12:71666076 | A | C | 1 | a0001c0001t0003g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+1496A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666076 | |||||||
| chr12:71666108 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.71+1528A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666108 | |||||||
| chr12:71666109 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.71+1529T>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666109 | |||||||
| chr12:71666110 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.71+1530T>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666110 | |||||||
| chr12:71666166 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.71+1586T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666166 | |||||||
| chr12:71666267 | C | T | 1 | a0001c0001t0008g0025 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.71+1687C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666267 | |||||||
| chr12:71666283 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.71+1703G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666283 | |||||||
| chr12:71666493 | A | G | 1 | a0001c0001t0003g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+1913A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666493 | |||||||
| chr12:71666580 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.71+2000G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666580 | |||||||
| chr12:71666619 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.71+2039A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666619 | |||||||
| chr12:71666686 | A | T | 8 | a0001c0001t0002g0055 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
14 | HG01496.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+2106A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666686 | |||||||
| chr12:71666984 | G | A | 1 | a0001c0001t0005g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.71+2404G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71666984 | |||||||
| chr12:71667005 | T | C | 1 | a0001c0001t0005g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71+2425T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71667005 | |||||||
| chr12:71667226 | C | G | 2 | a0002c0002t0003g0007 a0002c0002t0003g0056 |
9 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+2646C>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71667226 | |||||||
| chr12:71667243 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71+2663T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71667243 | |||||||
| chr12:71667269 | G | A | 1 | a0006c0010t0019g0063 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.71+2689G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71667269 | |||||||
| chr12:71667514 | A | G | 8 | a0001c0001t0002g0055 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
14 | HG01496.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+2934A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71667514 | |||||||
| chr12:71668051 | A | C | 1 | a0001c0001t0002g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.71+3471A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71668051 | |||||||
| chr12:71668113 | G | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.71+3533G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71668113 | |||||||
| chr12:71668241 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71+3661A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71668241 | |||||||
| chr12:71668259 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.71+3679T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71668259 | |||||||
| chr12:71668469 | T | TA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
259 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.71+3893dupA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71668469 | ||||||
| chr12:71668833 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.71+4253A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71668833 | |||||||
| chr12:71668945 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71+4365A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71668945 | |||||||
| chr12:71669247 | A | G | 1 | a0001c0001t0018g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+4667A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669247 | |||||||
| chr12:71669290 | C | T | 8 | a0001c0001t0002g0055 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
14 | HG01496.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+4710C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669290 | |||||||
| chr12:71669307 | G | C | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71+4727G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669307 | |||||||
| chr12:71669382 | C | A | 8 | a0001c0001t0002g0055 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
14 | HG01496.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+4802C>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669382 | |||||||
| chr12:71669398 | C | T | 4 | a0001c0001t0003g0022 a0001c0001t0003g0031 a0001c0001t0003g0052 others(1): Show |
6 | HG01496.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-4805C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669398 | |||||||
| chr12:71669410 | G | C | 1 | a0001c0001t0003g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.72-4793G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669410 | |||||||
| chr12:71669502 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
78 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.72-4701G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669502 | |||||||
| chr12:71669722 | G | A | 1 | a0001c0001t0003g0027 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.72-4481G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669722 | |||||||
| chr12:71669875 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
254 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.72-4328C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669875 | |||||||
| chr12:71669932 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.72-4271C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71669932 | |||||||
| chr12:71669957 | C | CA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
251 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.72-4230dupA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71669957 | ||||||
| chr12:71669957 | C | CAA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0049 others(3): Show |
12 | HG00597.hp1 HG01978.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-4231_72-4230dup others(2): Show |
THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71669957 | ||||||
| chr12:71670067 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
225 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.72-4136G>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670067 | |||||||
| chr12:71670423 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.72-3780G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670423 | |||||||
| chr12:71670506 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72-3697G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670506 | |||||||
| chr12:71670587 | T | G | 2 | a0002c0002t0003g0007 a0002c0002t0003g0056 |
9 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-3616T>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670587 | |||||||
| chr12:71670588 | A | G | 1 | a0002c0002t0003g0056 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.72-3615A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670588 | |||||||
| chr12:71670620 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.72-3583G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670620 | |||||||
| chr12:71670637 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0089 a0001c0001t0001g0090 |
5 | HG00280.hp2 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-3566A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670637 | |||||||
| chr12:71670800 | G | A | 1 | a0001c0001t0008g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.72-3403G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71670800 | |||||||
| chr12:71670936 | C | CA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(68): Show |
229 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.72-3248dupA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71670936 | ||||||
| chr12:71670936 | C | CAA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0004g0005 others(3): Show |
19 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.72-3249_72-3248dup others(2): Show |
THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71670936 | ||||||
| chr12:71670936 | CA | C | 4 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0002c0002t0003g0007 others(1): Show |
13 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-3248delA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71670936 | ||||||
| chr12:71671091 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.72-3112A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671091 | |||||||
| chr12:71671132 | C | T | 1 | a0002c0002t0003g0066 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.72-3071C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671132 | |||||||
| chr12:71671262 | G | C | 1 | a0001c0001t0008g0025 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.72-2941G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671262 | |||||||
| chr12:71671301 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.72-2902A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671301 | |||||||
| chr12:71671519 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.72-2684A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671519 | |||||||
| chr12:71671549 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
239 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.72-2654G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671549 | |||||||
| chr12:71671566 | G | T | 3 | a0002c0002t0003g0007 a0002c0002t0003g0056 a0002c0002t0003g0066 |
10 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-2637G>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671566 | |||||||
| chr12:71671622 | T | C | 8 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
12 | HG01496.hp1 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-2581T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671622 | |||||||
| chr12:71671780 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72-2423G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671780 | |||||||
| chr12:71671837 | A | C | 11 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0031 others(8): Show |
22 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.72-2366A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71671837 | |||||||
| chr12:71672208 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
276 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.72-1995G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672208 | |||||||
| chr12:71672370 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.72-1833G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672370 | |||||||
| chr12:71672631 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.72-1572G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672631 | |||||||
| chr12:71672635 | A | AT | 8 | a0001c0001t0001g0042 a0001c0001t0001g0083 a0001c0001t0001g0086 others(5): Show |
11 | HG01358.hp2 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-1556dupT | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71672635 | ||||||
| chr12:71672716 | C | CAT | 9 | a0001c0001t0002g0008 a0001c0001t0002g0023 a0001c0001t0003g0022 others(6): Show |
18 | HG01167.hp1 HG01496.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.72-1472_72-1471dup others(2): Show |
THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71672716 | ||||||
| chr12:71672716 | C | CATAT | 2 | a0001c0001t0003g0019 a0001c0001t0003g0052 |
4 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1474_72-1471dup others(4): Show |
THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71672716 | ||||||
| chr12:71672731 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72-1472A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672731 | |||||||
| chr12:71672814 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0089 a0001c0001t0001g0090 |
5 | HG00280.hp2 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-1389G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672814 | |||||||
| chr12:71672872 | C | T | 3 | a0002c0002t0003g0007 a0002c0002t0003g0056 a0002c0002t0003g0066 |
10 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-1331C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672872 | |||||||
| chr12:71672956 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.72-1247A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672956 | |||||||
| chr12:71672984 | G | C | 8 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
12 | HG01496.hp1 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-1219G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71672984 | |||||||
| chr12:71673072 | A | G | 4 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0053 others(1): Show |
14 | HG01069.hp1 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.72-1131A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673072 | |||||||
| chr12:71673073 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.72-1130T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673073 | |||||||
| chr12:71673307 | G | A | 1 | a0001c0001t0013g0078 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.72-896G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673307 | |||||||
| chr12:71673382 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.72-821A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673382 | |||||||
| chr12:71673816 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.72-387A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673816 | |||||||
| chr12:71673861 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.72-342G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673861 | |||||||
| chr12:71673878 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.72-325G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673878 | |||||||
| chr12:71673879 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.72-324C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673879 | |||||||
| chr12:71673972 | T | C | 3 | a0002c0002t0003g0007 a0002c0002t0003g0056 a0002c0002t0003g0066 |
10 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-231T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71673972 | |||||||
| chr12:71674151 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01361.hp1 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-52G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71674151 | |||||||
| chr12:71674152 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01361.hp1 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-51C>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | chr12 | 71674152 | |||||||
| chr12:71674186 | A | AT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
261 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
splice_region_variant&intron_variant | LOW | c.72-4dupT | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71674186 | ||||||
| chr12:71674186 | A | ATT | 6 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0031 others(3): Show |
9 | HG01891.hp1 HG02486.hp2 HG02717.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.72-5_72-4dupTT | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 71674186 | ||||||
| chr12:71674523 | G | A | 1 | a0001c0001t0006g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.267+125G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71674523 | |||||||
| chr12:71674719 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.267+321A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71674719 | |||||||
| chr12:71674750 | G | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0051 |
8 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.267+352G>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71674750 | |||||||
| chr12:71674798 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0069 |
4 | HG01109.hp1 HG03239.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+400G>A | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71674798 | |||||||
| chr12:71674909 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.267+511A>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71674909 | |||||||
| chr12:71674997 | CA | C | 12 | a0001c0001t0001g0068 a0001c0001t0003g0019 a0001c0001t0003g0022 others(9): Show |
23 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.267+607delA | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 71674997 | ||||||
| chr12:71675013 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.267+615A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71675013 | |||||||
| chr12:71675694 | C | T | 8 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0031 others(5): Show |
12 | HG01496.hp1 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.268-995C>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71675694 | |||||||
| chr12:71675885 | A | G | 1 | a0001c0001t0011g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.268-804A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71675885 | |||||||
| chr12:71676002 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01261.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.268-687A>G | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71676002 | |||||||
| chr12:71676279 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(94): Show |
281 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.268-410T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71676279 | |||||||
| chr12:71676287 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.268-402T>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71676287 | |||||||
| chr12:71676336 | A | T | 1 | a0008c0009t0002g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.268-353A>T | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71676336 | |||||||
| chr12:71676377 | G | C | 2 | a0001c0001t0008g0074 a0001c0001t0008g0084 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.268-312G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71676377 | |||||||
| chr12:71676516 | G | C | 1 | a0001c0001t0002g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.268-173G>C | THAP2 | ENSG00000173451.7 | transcript | ENST00000308086.3 | protein_coding | 2/2 | chr12 | 71676516 |