Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79725 |
| ensemblid | ENSG00000168152.13 |
| hgncid | 23192 |
| symbol | THAP9 |
| name | THAP domain containing 9 |
| refseq_nuc | NM_024672.6 |
| refseq_prot | NP_078948.3 |
| ensembl_nuc | ENST00000302236.10 |
| ensembl_prot | ENSP00000305533.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 82900735 |
| end | 82919969 |
| strand | + |
| ver | v1.2 |
| region | chr4:82900735-82919969 |
| region5000 | chr4:82895735-82924969 |
| regionname0 | THAP9_chr4_82900735_82919969 |
| regionname5000 | THAP9_chr4_82895735_82924969 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 903 | 258 | 65 | 25 | 139 | 4 | 25 | 109 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0002 | 0/1 | 903 | 108 | 2 | 34 | 52 | 4 | 15 | 42 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0003 | 0/0 | 903 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0004 | 0/0 | 903 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0005 | 1/0 | 903 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0006 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0007 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0008 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0009 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0010 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0011 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| a0012 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | MTRSC others(898): Show |
chr4 | 82895735 | 82924969 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2709 | 250 | 65 | 24 | 132 | 4 | 25 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0001c0004 | 0/0 | 2709 | 6 | 0 | 0 | 6 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0001c0007 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0001c0016 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0002c0002 | 0/1 | 2709 | 104 | 2 | 33 | 49 | 4 | 15 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0002c0013 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0002c0014 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0002c0017 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0002c0019 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0003c0003 | 0/0 | 2709 | 9 | 9 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0004c0005 | 0/0 | 2709 | 4 | 4 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0005c0006 | 1/0 | 2709 | 2 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0006c0010 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0007c0018 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0008c0011 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0009c0008 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0010c0015 | 0/0 | 2709 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0011c0009 | 0/0 | 2709 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 | ||
| a0012c0012 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | ATGAC others(2704): Show |
chr4 | 82895735 | 82924969 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3825 | 239 | 56 | 24 | 130 | 4 | 25 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0001t0002 | 0/0 | 3825 | 4 | 3 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0001t0003 | 0/0 | 3825 | 4 | 4 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0001t0004 | 0/0 | 3825 | 2 | 2 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0001t0005 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0004t0001 | 0/0 | 3825 | 6 | 0 | 0 | 6 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0007t0001 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0001c0016t0001 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0002t0002 | 0/1 | 3825 | 101 | 2 | 33 | 48 | 3 | 14 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0002t0006 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0002t0007 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 1 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0002t0008 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0013t0002 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0014t0002 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0017t0002 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0002c0019t0002 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0003c0003t0002 | 0/0 | 3825 | 9 | 9 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0004c0005t0002 | 0/0 | 3825 | 4 | 4 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0005c0006t0002 | 1/0 | 3825 | 2 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0006c0010t0001 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0007c0018t0002 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0008c0011t0001 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0009c0008t0001 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0010c0015t0002 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0011c0009t0001 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| a0012c0012t0002 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | GGAGC others(3820): Show |
chr4 | 82895735 | 82924969 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 64 | 19 | 9 | 25 | 2 | 9 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0003 | 0/0 | 37 | 11 | 2 | 20 | 1 | 3 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0006 | 0/0 | 9 | 3 | 0 | 5 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0011 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0004t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0007t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0001c0016t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0002 | 0/0 | 46 | 1 | 13 | 23 | 3 | 6 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0004 | 0/0 | 18 | 0 | 9 | 9 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0002g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0002t0008g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0013t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0014t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0017t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0002c0019t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0003c0003t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0003c0003t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0003c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0003c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0004c0005t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0005c0006t0002g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0005c0006t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0006c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0007c0018t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0008c0011t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0009c0008t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0010c0015t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0011c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| a0012c0012t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00438 | hp2 | a0006 | c0010 | t0001 | g0003 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00639 | hp1 | a0002 | c0017 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01884 | hp2 | a0005 | c0006 | t0002 | g0095 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01934 | hp2 | a0007 | c0018 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02004 | hp2 | a0001 | c0016 | t0001 | g0026 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02015 | hp1 | a0002 | c0002 | t0006 | g0032 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02027 | hp1 | a0001 | c0007 | t0001 | g0006 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0028 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02074 | hp1 | a0008 | c0011 | t0001 | g0051 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CDX | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | PEL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02622 | hp1 | a0004 | c0005 | t0002 | g0016 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02630 | hp2 | a0004 | c0005 | t0002 | g0016 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0036 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0019 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0019 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02965 | hp1 | a0004 | c0005 | t0002 | g0016 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02976 | hp1 | a0004 | c0005 | t0002 | g0016 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03041 | hp2 | a0003 | c0003 | t0002 | g0094 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03130 | hp2 | a0003 | c0003 | t0002 | g0023 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0036 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03195 | hp2 | a0009 | c0008 | t0001 | g0003 | AFR | ESN | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03239 | hp1 | a0010 | c0015 | t0002 | g0002 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03490 | hp1 | a0002 | c0002 | t0008 | g0015 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0019 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0085 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0097 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04199 | hp1 | a0011 | c0009 | t0001 | g0001 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18612 | hp1 | a0002 | c0013 | t0002 | g0002 | EAS | CHB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18906 | hp2 | a0003 | c0003 | t0002 | g0023 | AFR | YRI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18953 | hp1 | a0001 | c0004 | t0001 | g0064 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18965 | hp1 | a0002 | c0014 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18984 | hp1 | a0012 | c0012 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18990 | hp1 | a0002 | c0019 | t0002 | g0100 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19064 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0028 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19240 | hp1 | a0003 | c0003 | t0002 | g0043 | AFR | YRI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA20752 | hp2 | a0002 | c0002 | t0007 | g0015 | EUR | TSI | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0035 | SAS | GIH | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | USA | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0101 | REF | REF | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| homoSapiens | grch38p0 | a0005 | c0006 | t0002 | g0093 | REF | REF | THAP9_chr4_82895735_82924969 | THAP9 | chr4 | 82895735 | 82924969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82906433 | A | G | 1 | a0007 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.386A>G | p.Lys129Arg | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/5 | 454/3825 | 386/2712 | 129/903 | chr4 | 82906433 | |||
| chr4:82906448 | T | C | 1 | a0004 | 4 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.401T>C | p.Ile134Thr | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/5 | 469/3825 | 401/2712 | 134/903 | chr4 | 82906448 | |||
| chr4:82917064 | G | A | 10 | a0001 a0002 a0004 others(7): Show |
376 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(373): Show |
missense_variant | MODERATE | c.852G>A | p.Met284Ile | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 920/3825 | 852/2712 | 284/903 | chr4 | 82917064 | |||
| chr4:82917109 | G | T | 5 | a0002 a0004 a0007 others(2): Show |
114 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(111): Show |
missense_variant | MODERATE | c.897G>T | p.Leu299Phe | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 965/3825 | 897/2712 | 299/903 | chr4 | 82917109 | |||
| chr4:82917432 | A | G | 1 | a0010 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1220A>G | p.Gln407Arg | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 1288/3825 | 1220/2712 | 407/903 | chr4 | 82917432 | |||
| chr4:82918280 | G | T | 1 | a0008 | 1 | HG02074.hp1 | stop_gained | HIGH | c.2068G>T | p.Glu690* | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2136/3825 | 2068/2712 | 690/903 | chr4 | 82918280 | |||
| chr4:82918281 | A | T | 1 | a0008 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.2069A>T | p.Glu690Val | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2137/3825 | 2069/2712 | 690/903 | chr4 | 82918281 | |||
| chr4:82918295 | G | A | 1 | a0009 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.2083G>A | p.Asp695Asn | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2151/3825 | 2083/2712 | 695/903 | chr4 | 82918295 | |||
| chr4:82918347 | G | A | 1 | a0012 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2135G>A | p.Arg712Lys | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2203/3825 | 2135/2712 | 712/903 | chr4 | 82918347 | |||
| chr4:82918542 | G | A | 1 | a0011 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2330G>A | p.Arg777Gln | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2398/3825 | 2330/2712 | 777/903 | chr4 | 82918542 | |||
| chr4:82918646 | A | G | 10 | a0001 a0002 a0004 others(7): Show |
376 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(373): Show |
missense_variant | MODERATE | c.2434A>G | p.Asn812Asp | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2502/3825 | 2434/2712 | 812/903 | chr4 | 82918646 | |||
| chr4:82918689 | T | G | 1 | a0006 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.2477T>G | p.Val826Gly | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2545/3825 | 2477/2712 | 826/903 | chr4 | 82918689 | |||
| chr4:82918709 | G | A | 1 | a0003 | 9 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
missense_variant | MODERATE | c.2497G>A | p.Val833Ile | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2565/3825 | 2497/2712 | 833/903 | chr4 | 82918709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82904766 | A | G | 1 | a0002c0019 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.111A>G | p.Lys37Lys | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/5 | 179/3825 | 111/2712 | 37/903 | chr4 | 82904766 | |||
| chr4:82907858 | A | G | 2 | a0001c0016 a0002c0017 |
2 | HG00639.hp1 HG02004.hp2 |
synonymous_variant | LOW | c.654A>G | p.Thr218Thr | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/5 | 722/3825 | 654/2712 | 218/903 | chr4 | 82907858 | |||
| chr4:82917047 | T | C | 1 | a0001c0007 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.835T>C | p.Leu279Leu | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 903/3825 | 835/2712 | 279/903 | chr4 | 82917047 | |||
| chr4:82917847 | C | T | 1 | a0001c0004 | 6 | HG02071.hp1 NA18953.hp1 NA18983.hp1 others(3): Show |
synonymous_variant | LOW | c.1635C>T | p.His545His | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 1703/3825 | 1635/2712 | 545/903 | chr4 | 82917847 | |||
| chr4:82918237 | A | G | 1 | a0002c0014 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.2025A>G | p.Gln675Gln | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2093/3825 | 2025/2712 | 675/903 | chr4 | 82918237 | |||
| chr4:82918276 | C | T | 1 | a0002c0013 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.2064C>T | p.His688His | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2132/3825 | 2064/2712 | 688/903 | chr4 | 82918276 | |||
| chr4:82918903 | C | T | 1 | a0004c0005 | 4 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.2691C>T | p.Asn897Asn | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 2759/3825 | 2691/2712 | 897/903 | chr4 | 82918903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82900755 | T | A | 1 | a0001c0001t0005 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/5 | 48 | chr4 | 82900755 | ||||||
| chr4:82900756 | C | T | 1 | a0001c0001t0005 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/5 | 47 | chr4 | 82900756 | ||||||
| chr4:82900798 | A | C | 1 | a0001c0001t0003 | 4 | HG01891.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-5A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/5 | 5 | chr4 | 82900798 | ||||||
| chr4:82919328 | T | C | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(7): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*404T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 404 | chr4 | 82919328 | ||||||
| chr4:82919753 | G | A | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(7): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*829G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 829 | chr4 | 82919753 | ||||||
| chr4:82919756 | A | C | 1 | a0001c0001t0004 | 2 | HG02572.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*832A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 832 | chr4 | 82919756 | ||||||
| chr4:82919766 | A | G | 1 | a0002c0002t0008 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 842 | chr4 | 82919766 | ||||||
| chr4:82919856 | T | G | 1 | a0002c0002t0006 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932T>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 932 | chr4 | 82919856 | ||||||
| chr4:82919941 | A | G | 1 | a0002c0002t0007 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 5/5 | 1017 | chr4 | 82919941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82901070 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.80+188G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901070 | |||||||
| chr4:82901110 | T | C | 2 | a0003c0003t0002g0023 a0003c0003t0002g0043 |
3 | HG03130.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.80+228T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901110 | |||||||
| chr4:82901123 | A | G | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.80+241A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901123 | |||||||
| chr4:82901141 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.80+259T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901141 | |||||||
| chr4:82901181 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
165 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.80+299G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901181 | |||||||
| chr4:82901304 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(31): Show |
100 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.80+422C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901304 | |||||||
| chr4:82901672 | TTAGAGTA others(7): Show |
T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.80+794_80+807delAG others(12): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82901672 | ||||||
| chr4:82901674 | A | C | 39 | a0001c0001t0002g0002 a0002c0002t0002g0002 a0002c0002t0002g0004 others(36): Show |
111 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.80+792A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901674 | |||||||
| chr4:82901706 | A | T | 1 | a0002c0019t0002g0100 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.80+824A>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901706 | |||||||
| chr4:82901710 | AT | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
366 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(363): Show |
intron_variant | MODIFIER | c.80+843delT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82901710 | ||||||
| chr4:82901721 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(81): Show |
259 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.80+839T>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901721 | |||||||
| chr4:82901721 | T | TG | 1 | a0003c0003t0002g0019 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80+839_80+840insG | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901721 | |||||||
| chr4:82901722 | T | G | 2 | a0001c0001t0002g0079 a0002c0002t0002g0078 |
2 | HG03209.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.80+840T>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901722 | |||||||
| chr4:82901788 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+906C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901788 | |||||||
| chr4:82901806 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.80+924A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901806 | |||||||
| chr4:82901962 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.80+1080G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82901962 | |||||||
| chr4:82902063 | A | AGTTAT | 3 | a0001c0001t0001g0022 a0001c0001t0001g0114 a0001c0001t0001g0115 |
5 | HG00140.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+1183_80+1187dup others(5): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82902063 | ||||||
| chr4:82902105 | C | CT | 35 | a0001c0001t0001g0103 a0001c0001t0002g0002 a0001c0001t0002g0079 others(32): Show |
88 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.80+1243dupT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82902105 | ||||||
| chr4:82902105 | C | CTT | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(38): Show |
132 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.80+1242_80+1243dup others(2): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82902105 | ||||||
| chr4:82902105 | C | CTTT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(37): Show |
138 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.80+1241_80+1243dup others(3): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82902105 | ||||||
| chr4:82902105 | C | CTTTT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
14 | HG00621.hp1 HG02027.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.80+1240_80+1243dup others(4): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82902105 | ||||||
| chr4:82902193 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80+1311C>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902193 | |||||||
| chr4:82902235 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
376 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.80+1353G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902235 | |||||||
| chr4:82902260 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.80+1378C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902260 | |||||||
| chr4:82902263 | C | CT | 6 | a0001c0001t0001g0066 a0001c0001t0002g0079 a0001c0001t0002g0116 others(3): Show |
6 | HG02886.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+1395dupT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82902263 | ||||||
| chr4:82902407 | A | G | 1 | a0002c0002t0002g0089 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.80+1525A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902407 | |||||||
| chr4:82902431 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.80+1549C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902431 | |||||||
| chr4:82902550 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0044 others(1): Show |
12 | HG00438.hp1 HG00673.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+1668G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902550 | |||||||
| chr4:82902941 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.81-1795G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902941 | |||||||
| chr4:82902988 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.81-1748A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82902988 | |||||||
| chr4:82903034 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.81-1702A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903034 | |||||||
| chr4:82903039 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81-1697T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903039 | |||||||
| chr4:82903046 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.81-1690C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903046 | |||||||
| chr4:82903216 | C | T | 1 | a0001c0001t0004g0076 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.81-1520C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903216 | |||||||
| chr4:82903261 | C | T | 1 | a0005c0006t0002g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81-1475C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903261 | |||||||
| chr4:82903262 | G | T | 1 | a0002c0002t0002g0010 | 6 | NA18955.hp1 NA18994.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-1474G>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903262 | |||||||
| chr4:82903501 | C | T | 1 | a0002c0002t0002g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.81-1235C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903501 | |||||||
| chr4:82903566 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81-1170A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903566 | |||||||
| chr4:82903842 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.81-894A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903842 | |||||||
| chr4:82903887 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.81-849G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903887 | |||||||
| chr4:82903904 | A | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0074 |
4 | HG01891.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-832A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903904 | |||||||
| chr4:82903957 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.81-779G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82903957 | |||||||
| chr4:82904057 | CCTTTT | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0102 |
5 | HG01928.hp1 HG01978.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-678_81-674delCT others(3): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904057 | |||||||
| chr4:82904058 | CT | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
235 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.81-655delT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82904058 | ||||||
| chr4:82904058 | CTT | C | 7 | a0001c0001t0002g0117 a0002c0002t0002g0002 a0002c0002t0002g0004 others(4): Show |
30 | HG00609.hp1 HG01109.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.81-656_81-655delTT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82904058 | ||||||
| chr4:82904058 | CTTTTT | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
88 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.81-659_81-655delTT others(3): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 82904058 | ||||||
| chr4:82904060 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81-676T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904060 | |||||||
| chr4:82904061 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81-675T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904061 | |||||||
| chr4:82904064 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-672T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904064 | |||||||
| chr4:82904156 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.81-580C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904156 | |||||||
| chr4:82904222 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
377 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(374): Show |
intron_variant | MODIFIER | c.81-514T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904222 | |||||||
| chr4:82904308 | C | T | 1 | a0004c0005t0002g0016 | 4 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-428C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904308 | |||||||
| chr4:82904429 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0105 |
5 | NA18612.hp2 NA18949.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-307T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904429 | |||||||
| chr4:82904493 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.81-243A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904493 | |||||||
| chr4:82904517 | G | T | 4 | a0001c0004t0001g0028 a0001c0004t0001g0063 a0001c0004t0001g0064 others(1): Show |
5 | HG02071.hp1 NA18953.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-219G>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904517 | |||||||
| chr4:82904670 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.81-66A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 1/4 | chr4 | 82904670 | |||||||
| chr4:82905075 | T | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0073 others(2): Show |
9 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+144T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | chr4 | 82905075 | |||||||
| chr4:82905214 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0073 others(2): Show |
9 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+283A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | chr4 | 82905214 | |||||||
| chr4:82905258 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0066 a0001c0001t0001g0070 |
4 | HG02165.hp1 NA18949.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+327A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | chr4 | 82905258 | |||||||
| chr4:82905304 | T | C | 1 | a0001c0001t0001g0017 | 3 | NA18993.hp1 NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.276+373T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | chr4 | 82905304 | |||||||
| chr4:82905962 | A | G | 1 | a0002c0002t0002g0087 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.277-362A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | chr4 | 82905962 | |||||||
| chr4:82906136 | C | CA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.277-177dupA | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 82906136 | ||||||
| chr4:82906315 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02080.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.277-9C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 2/4 | chr4 | 82906315 | |||||||
| chr4:82906640 | A | G | 1 | a0005c0006t0002g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580+13A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82906640 | |||||||
| chr4:82906669 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.580+42A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82906669 | |||||||
| chr4:82906870 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.580+243A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82906870 | |||||||
| chr4:82907041 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.580+414G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907041 | |||||||
| chr4:82907075 | C | T | 1 | a0005c0006t0002g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580+448C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907075 | |||||||
| chr4:82907306 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.581-479A>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907306 | |||||||
| chr4:82907351 | AT | A | 39 | a0001c0001t0002g0002 a0002c0002t0002g0002 a0002c0002t0002g0004 others(36): Show |
111 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.581-422delT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 82907351 | ||||||
| chr4:82907353 | T | A | 1 | a0005c0006t0002g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.581-432T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907353 | |||||||
| chr4:82907520 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.581-265T>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907520 | |||||||
| chr4:82907719 | A | G | 1 | a0002c0002t0002g0035 | 2 | NA20300.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.581-66A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907719 | |||||||
| chr4:82907749 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.581-36A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 3/4 | chr4 | 82907749 | |||||||
| chr4:82907959 | T | A | 3 | a0001c0001t0002g0079 a0001c0001t0002g0116 a0001c0001t0002g0117 |
3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.731+24T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82907959 | |||||||
| chr4:82908027 | ATAT | A | 3 | a0001c0001t0002g0079 a0001c0001t0002g0116 a0001c0001t0002g0117 |
3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.731+97_731+99delAT others(1): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82908027 | ||||||
| chr4:82908084 | TA | T | 39 | a0001c0001t0002g0002 a0002c0002t0002g0002 a0002c0002t0002g0004 others(36): Show |
111 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.731+156delA | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82908084 | ||||||
| chr4:82908353 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.731+418C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82908353 | |||||||
| chr4:82908412 | ATGCC | A | 3 | a0001c0001t0002g0079 a0001c0001t0002g0116 a0001c0001t0002g0117 |
3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.731+478_731+481del others(4): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82908412 | |||||||
| chr4:82908565 | C | T | 1 | a0002c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.731+630C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82908565 | |||||||
| chr4:82908650 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.731+715C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82908650 | |||||||
| chr4:82908911 | CT | C | 40 | a0001c0001t0002g0002 a0002c0002t0002g0002 a0002c0002t0002g0004 others(37): Show |
115 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.731+987delT | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82908911 | ||||||
| chr4:82908912 | T | A | 1 | a0001c0001t0001g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.731+977T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82908912 | |||||||
| chr4:82909091 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
156 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.731+1156G>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909091 | |||||||
| chr4:82909143 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.731+1208G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909143 | |||||||
| chr4:82909267 | A | G | 1 | a0002c0002t0002g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.731+1332A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909267 | |||||||
| chr4:82909408 | A | G | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.731+1473A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909408 | |||||||
| chr4:82909422 | C | CTG | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(34): Show |
103 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.731+1504_731+1505d others(4): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82909422 | ||||||
| chr4:82909422 | C | CTGTG | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
141 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.731+1502_731+1505d others(6): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82909422 | ||||||
| chr4:82909440 | G | GTGTA | 1 | a0001c0001t0001g0014 | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.731+1505_731+1506i others(6): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909440 | |||||||
| chr4:82909493 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.731+1558C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909493 | |||||||
| chr4:82909539 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.731+1604G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909539 | |||||||
| chr4:82909601 | A | G | 1 | a0001c0001t0001g0021 | 3 | HG03654.hp2 HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.731+1666A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909601 | |||||||
| chr4:82909617 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.731+1682C>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909617 | |||||||
| chr4:82909976 | A | C | 1 | a0001c0001t0001g0031 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.731+2041A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82909976 | |||||||
| chr4:82910143 | C | A | 5 | a0002c0002t0002g0015 a0002c0002t0002g0081 a0002c0002t0002g0090 others(2): Show |
6 | HG01168.hp1 HG01433.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.731+2208C>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910143 | |||||||
| chr4:82910364 | A | C | 1 | a0002c0002t0002g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.731+2429A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910364 | |||||||
| chr4:82910367 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
376 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.731+2432T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910367 | |||||||
| chr4:82910376 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.731+2441G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910376 | |||||||
| chr4:82910377 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.731+2442C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910377 | |||||||
| chr4:82910438 | T | TAA | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.731+2513_731+2514d others(4): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82910438 | ||||||
| chr4:82910438 | TA | T | 40 | a0001c0001t0002g0002 a0002c0002t0002g0002 a0002c0002t0002g0004 others(37): Show |
115 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.731+2514delA | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82910438 | ||||||
| chr4:82910479 | T | C | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.731+2544T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910479 | |||||||
| chr4:82910535 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.731+2600G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910535 | |||||||
| chr4:82910571 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG00609.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.731+2636T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910571 | |||||||
| chr4:82910578 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.731+2643A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910578 | |||||||
| chr4:82910889 | G | A | 1 | a0008c0011t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.731+2954G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910889 | |||||||
| chr4:82910958 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.731+3023A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82910958 | |||||||
| chr4:82911015 | T | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0073 others(2): Show |
9 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.731+3080T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911015 | |||||||
| chr4:82911123 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.731+3188G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911123 | |||||||
| chr4:82911301 | T | TG | 45 | a0001c0001t0002g0002 a0001c0001t0002g0079 a0001c0001t0002g0116 others(42): Show |
120 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.731+3370dupG | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82911301 | ||||||
| chr4:82911374 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
3 | HG02165.hp2 NA18946.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.731+3439G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911374 | |||||||
| chr4:82911389 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.731+3454A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911389 | |||||||
| chr4:82911567 | C | G | 1 | a0008c0011t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.731+3632C>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911567 | |||||||
| chr4:82911589 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0003g0018 others(1): Show |
7 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.731+3654G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911589 | |||||||
| chr4:82911608 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.731+3673G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911608 | |||||||
| chr4:82911658 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.731+3723C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911658 | |||||||
| chr4:82911685 | G | A | 1 | a0001c0001t0001g0017 | 3 | NA18993.hp1 NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.731+3750G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911685 | |||||||
| chr4:82911735 | C | T | 1 | a0005c0006t0002g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.731+3800C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911735 | |||||||
| chr4:82911739 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.731+3804G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911739 | |||||||
| chr4:82911760 | T | C | 1 | a0002c0002t0002g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.731+3825T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911760 | |||||||
| chr4:82911966 | A | G | 1 | a0003c0003t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.731+4031A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82911966 | |||||||
| chr4:82912016 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.731+4081A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912016 | |||||||
| chr4:82912068 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.731+4133C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912068 | |||||||
| chr4:82912320 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.731+4385T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912320 | |||||||
| chr4:82912393 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0069 |
2 | NA18994.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.731+4458C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912393 | |||||||
| chr4:82912550 | G | A | 2 | a0002c0002t0002g0083 a0005c0006t0002g0095 |
2 | HG01884.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.732-4394G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912550 | |||||||
| chr4:82912623 | G | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(31): Show |
100 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.732-4321G>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912623 | |||||||
| chr4:82912635 | A | T | 1 | a0002c0002t0002g0034 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.732-4309A>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912635 | |||||||
| chr4:82912710 | C | A | 39 | a0001c0001t0002g0002 a0002c0002t0002g0002 a0002c0002t0002g0004 others(36): Show |
111 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.732-4234C>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912710 | |||||||
| chr4:82912758 | A | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
376 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.732-4186A>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912758 | |||||||
| chr4:82912781 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.732-4163A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912781 | |||||||
| chr4:82912899 | G | A | 1 | a0002c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.732-4045G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912899 | |||||||
| chr4:82912991 | G | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.732-3953G>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82912991 | |||||||
| chr4:82913001 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0044 |
3 | NA18980.hp2 NA19062.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.732-3943C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913001 | |||||||
| chr4:82913253 | A | C | 1 | a0002c0002t0002g0084 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.732-3691A>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913253 | |||||||
| chr4:82913457 | A | T | 1 | a0004c0005t0002g0016 | 4 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.732-3487A>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913457 | |||||||
| chr4:82913529 | T | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0003g0018 others(1): Show |
8 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.732-3415T>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913529 | |||||||
| chr4:82913569 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.732-3375T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913569 | |||||||
| chr4:82913592 | CA | C | 48 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0113 others(45): Show |
125 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.732-3351delA | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913592 | |||||||
| chr4:82913620 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(74): Show |
225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.732-3324A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913620 | |||||||
| chr4:82913635 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
373 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(370): Show |
intron_variant | MODIFIER | c.732-3309G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913635 | |||||||
| chr4:82913740 | T | A | 1 | a0001c0001t0001g0012 | 5 | HG02027.hp2 HG02080.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.732-3204T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913740 | |||||||
| chr4:82913891 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
376 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.732-3053T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913891 | |||||||
| chr4:82913895 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
255 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.732-3049C>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913895 | |||||||
| chr4:82913989 | G | A | 3 | a0002c0002t0002g0032 a0002c0002t0002g0096 a0002c0002t0006g0032 |
3 | HG00558.hp1 HG02015.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.732-2955G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82913989 | |||||||
| chr4:82914035 | C | T | 1 | a0008c0011t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.732-2909C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914035 | |||||||
| chr4:82914063 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.732-2881A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914063 | |||||||
| chr4:82914131 | C | G | 1 | a0002c0002t0002g0091 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.732-2813C>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914131 | |||||||
| chr4:82914133 | A | G | 2 | a0001c0004t0001g0064 a0001c0004t0001g0071 |
2 | NA18953.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.732-2811A>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914133 | |||||||
| chr4:82914545 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.732-2399C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914545 | |||||||
| chr4:82914808 | TACCTTAA others(9): Show |
T | 1 | a0001c0001t0001g0055 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.732-2131_732-2116d others(18): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82914808 | ||||||
| chr4:82914821 | T | TCCCACCT others(375): Show |
1 | a0002c0002t0002g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.732-2106_732-2105i others(384): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82914821 | ||||||
| chr4:82914843 | C | T | 2 | a0002c0002t0002g0033 a0002c0002t0002g0082 |
3 | HG00733.hp1 HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.732-2101C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914843 | |||||||
| chr4:82914914 | G | A | 1 | a0001c0004t0001g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.732-2030G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914914 | |||||||
| chr4:82914941 | T | C | 1 | a0001c0001t0001g0007 | 9 | HG02074.hp2 NA18940.hp1 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.732-2003T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82914941 | |||||||
| chr4:82915096 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(31): Show |
100 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.732-1848C>T | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915096 | |||||||
| chr4:82915239 | ATTGTTTT others(3): Show |
A | 51 | a0001c0001t0002g0002 a0001c0001t0002g0079 a0001c0001t0002g0116 others(48): Show |
130 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.732-1676_732-1667d others(12): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82915239 | ||||||
| chr4:82915239 | ATTGTTTT others(18): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.732-1691_732-1667d others(27): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82915239 | ||||||
| chr4:82915353 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0058 |
4 | HG02056.hp1 HG02165.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.732-1591T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915353 | |||||||
| chr4:82915469 | C | G | 1 | a0008c0011t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.732-1475C>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915469 | |||||||
| chr4:82915506 | C | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.732-1438C>G | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915506 | |||||||
| chr4:82915572 | T | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
156 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.732-1372T>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915572 | |||||||
| chr4:82915646 | T | C | 2 | a0001c0001t0001g0026 a0001c0016t0001g0026 |
2 | HG01346.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.732-1298T>C | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915646 | |||||||
| chr4:82915732 | TATATACA others(4): Show |
T | 1 | a0001c0001t0001g0020 | 3 | NA18612.hp2 NA18965.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.732-1211_732-1201d others(13): Show |
THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82915732 | |||||||
| chr4:82916119 | C | CA | 5 | a0003c0003t0002g0019 a0003c0003t0002g0023 a0003c0003t0002g0036 others(2): Show |
9 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.732-824dupA | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 82916119 | ||||||
| chr4:82916126 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.732-818G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82916126 | |||||||
| chr4:82916321 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.732-623G>A | THAP9 | ENSG00000168152.13 | transcript | ENST00000302236.10 | protein_coding | 4/4 | chr4 | 82916321 |