Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7507 |
| ensemblid | ENSG00000136936.11 |
| hgncid | 12814 |
| symbol | XPA |
| name | XPA, DNA damage recognition and repair factor |
| refseq_nuc | NM_000380.4 |
| refseq_prot | NP_000371.1 |
| ensembl_nuc | ENST00000375128.5 |
| ensembl_prot | ENSP00000364270.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 97674909 |
| end | 97697340 |
| strand | - |
| ver | v1.2 |
| region | chr9:97674909-97697340 |
| region5000 | chr9:97669909-97702340 |
| regionname0 | XPA_chr9_97674909_97697340 |
| regionname5000 | XPA_chr9_97669909_97702340 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 273 | 405 | 82 | 78 | 185 | 14 | 44 | 143 | XPA_chr9_97669909_97702340 | XPA | MAAAD others(268): Show |
chr9 | 97669909 | 97702340 |
| a0002 | 0/0 | 273 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | MAAAD others(268): Show |
chr9 | 97669909 | 97702340 |
| a0003 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | MAAAD others(268): Show |
chr9 | 97669909 | 97702340 |
| a0004 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | MAAAD others(268): Show |
chr9 | 97669909 | 97702340 |
| a0005 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | MAAAD others(268): Show |
chr9 | 97669909 | 97702340 |
| a0006 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | MAAAD others(268): Show |
chr9 | 97669909 | 97702340 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 819 | 405 | 82 | 78 | 185 | 14 | 44 | XPA_chr9_97669909_97702340 | XPA | ATGGC others(814): Show |
chr9 | 97669909 | 97702340 | ||
| a0002c0002 | 0/0 | 819 | 5 | 5 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | ATGGC others(814): Show |
chr9 | 97669909 | 97702340 | ||
| a0003c0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | ATGGC others(814): Show |
chr9 | 97669909 | 97702340 | ||
| a0004c0003 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | ATGGC others(814): Show |
chr9 | 97669909 | 97702340 | ||
| a0005c0005 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | ATGGC others(814): Show |
chr9 | 97669909 | 97702340 | ||
| a0006c0004 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | ATGGC others(814): Show |
chr9 | 97669909 | 97702340 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1400 | 169 | 12 | 24 | 101 | 5 | 25 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0002 | 0/0 | 1400 | 158 | 28 | 40 | 63 | 9 | 18 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0003 | 0/0 | 1400 | 35 | 1 | 12 | 21 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0004 | 0/0 | 1400 | 24 | 23 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0005 | 0/0 | 1400 | 15 | 14 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0006 | 0/0 | 1400 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0007 | 0/0 | 1400 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0001c0001t0008 | 0/0 | 1400 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0002c0002t0003 | 0/0 | 1400 | 5 | 5 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0003c0006t0004 | 0/0 | 1400 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0004c0003t0001 | 0/0 | 1400 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0005c0005t0002 | 0/0 | 1400 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| a0006c0004t0002 | 0/0 | 1400 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | AGTGC others(1395): Show |
chr9 | 97669909 | 97702340 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 23 | 1 | 2 | 20 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0003 | 0/0 | 20 | 0 | 3 | 17 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0005 | 0/0 | 17 | 0 | 1 | 12 | 1 | 3 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 2 | 2 | 0 | 5 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 1 | 4 | 1 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0014 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0022 | 1/1 | 4 | 0 | 1 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0027 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0001 | 0/0 | 33 | 1 | 5 | 27 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0008 | 0/0 | 9 | 0 | 2 | 5 | 1 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0009 | 0/0 | 9 | 0 | 1 | 2 | 2 | 4 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0011 | 0/0 | 8 | 0 | 7 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0013 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0016 | 0/0 | 6 | 0 | 1 | 0 | 1 | 4 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0017 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0019 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0020 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0025 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0059 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0060 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0004 | 0/0 | 18 | 0 | 11 | 6 | 0 | 1 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0010 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0007 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0006g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0001c0001t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0002c0002t0003g0024 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0002c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0003c0006t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0004c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0005c0005t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| a0006c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0140 | EUR | GBR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | GBR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | FIN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0106 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02145 | hp1 | a0003 | c0006 | t0004 | g0116 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CDX | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CDX | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | CDX | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0109 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03098 | hp2 | a0005 | c0005 | t0002 | g0139 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0117 | AFR | YRI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | YRI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18967 | hp2 | a0006 | c0004 | t0002 | g0141 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | LWK | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | YRI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0120 | AFR | YRI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ASW | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ASW | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | TSI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | GIH | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02486 | hp1 | a0004 | c0003 | t0001 | g0087 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | USA | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | USA | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | LWK | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | LWK | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0022 | REF | REF | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | XPA_chr9_97669909_97702340 | XPA | chr9 | 97669909 | 97702340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97675495 | T | C | 1 | a0002 | 5 | HG02109.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.766A>G | p.Met256Val | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 814/1400 | 766/822 | 256/273 | chr9 | 97675495 | |||
| chr9:97675507 | G | C | 1 | a0005 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.754C>G | p.Leu252Val | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 802/1400 | 754/822 | 252/273 | chr9 | 97675507 | |||
| chr9:97684948 | C | G | 1 | a0006 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.648G>C | p.Gln216His | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/6 | 696/1400 | 648/822 | 216/273 | chr9 | 97684948 | |||
| chr9:97687154 | A | G | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.497T>C | p.Val166Ala | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/6 | 545/1400 | 497/822 | 166/273 | chr9 | 97687154 | |||
| chr9:97687248 | T | C | 1 | a0003 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.403A>G | p.Lys135Glu | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/6 | 451/1400 | 403/822 | 135/273 | chr9 | 97687248 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97674916 | C | T | 1 | a0001c0001t0006 | 2 | HG02976.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*523G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 523 | chr9 | 97674916 | ||||||
| chr9:97675043 | A | C | 1 | a0001c0001t0008 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 396 | chr9 | 97675043 | ||||||
| chr9:97675161 | A | G | 1 | a0001c0001t0005 | 15 | HG01891.hp2 HG01952.hp2 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*278T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 278 | chr9 | 97675161 | ||||||
| chr9:97675205 | G | T | 2 | a0001c0001t0003 a0002c0002t0003 |
40 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*234C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 234 | chr9 | 97675205 | ||||||
| chr9:97675236 | G | C | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(4): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*203C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 203 | chr9 | 97675236 | ||||||
| chr9:97675369 | G | A | 1 | a0001c0001t0007 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 6/6 | 70 | chr9 | 97675369 | ||||||
| chr9:97697296 | T | C | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(240): Show |
5_prime_UTR_variant | MODIFIER | c.-4A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/6 | 4 | chr9 | 97697296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97675666 | A | G | 1 | a0001c0001t0006g0043 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.674-79T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97675666 | |||||||
| chr9:97675997 | T | A | 1 | a0001c0001t0004g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.674-410A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97675997 | |||||||
| chr9:97676062 | T | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0059 others(7): Show |
22 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.674-475A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676062 | |||||||
| chr9:97676285 | C | T | 1 | a0001c0001t0004g0042 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.674-698G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676285 | |||||||
| chr9:97676370 | A | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-783T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676370 | |||||||
| chr9:97676483 | T | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-896A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676483 | |||||||
| chr9:97676528 | A | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0050 a0001c0001t0002g0131 others(1): Show |
8 | HG01109.hp2 HG01243.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.674-941T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676528 | |||||||
| chr9:97676529 | T | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-942A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676529 | |||||||
| chr9:97676569 | T | TA | 3 | a0001c0001t0003g0121 a0002c0002t0003g0024 a0002c0002t0003g0120 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.674-983dupT | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676569 | |||||||
| chr9:97676681 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.674-1094T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676681 | |||||||
| chr9:97676751 | T | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0140 |
3 | HG00099.hp1 HG01168.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.674-1164A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676751 | |||||||
| chr9:97676942 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.674-1355A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97676942 | |||||||
| chr9:97677082 | T | TCACGTAA others(10): Show |
92 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(89): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.674-1496_674-1495i others(19): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677082 | |||||||
| chr9:97677272 | T | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-1685A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677272 | |||||||
| chr9:97677401 | C | T | 7 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(4): Show |
33 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.674-1814G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677401 | |||||||
| chr9:97677428 | G | C | 1 | a0001c0001t0002g0134 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.674-1841C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677428 | |||||||
| chr9:97677438 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.674-1851G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677438 | |||||||
| chr9:97677470 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.674-1883G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677470 | |||||||
| chr9:97677488 | C | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-1901G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677488 | |||||||
| chr9:97677537 | A | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-1950T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677537 | |||||||
| chr9:97677722 | G | C | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.674-2135C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677722 | |||||||
| chr9:97677752 | C | CTT | 12 | a0001c0001t0001g0078 a0001c0001t0003g0004 a0001c0001t0003g0010 others(9): Show |
41 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.674-2167_674-2166d others(4): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677752 | |||||||
| chr9:97677752 | C | CTTT | 15 | a0001c0001t0004g0007 a0001c0001t0004g0042 a0001c0001t0004g0044 others(12): Show |
33 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.674-2168_674-2166d others(5): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677752 | |||||||
| chr9:97677752 | C | CTTTT | 6 | a0001c0001t0004g0105 a0001c0001t0004g0110 a0001c0001t0004g0111 others(3): Show |
7 | HG01891.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-2169_674-2166d others(6): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677752 | |||||||
| chr9:97677786 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.674-2199T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677786 | |||||||
| chr9:97677854 | A | G | 1 | a0001c0001t0002g0143 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.674-2267T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97677854 | |||||||
| chr9:97678101 | C | G | 1 | a0001c0001t0002g0147 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.674-2514G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678101 | |||||||
| chr9:97678109 | G | A | 11 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(8): Show |
40 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.674-2522C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678109 | |||||||
| chr9:97678128 | T | C | 94 | a0001c0001t0001g0090 a0001c0001t0002g0001 a0001c0001t0002g0008 others(91): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.674-2541A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678128 | |||||||
| chr9:97678167 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.674-2580C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678167 | |||||||
| chr9:97678396 | G | A | 1 | a0001c0001t0004g0044 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.674-2809C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678396 | |||||||
| chr9:97678407 | AAAT | A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0048 |
10 | HG00741.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.674-2823_674-2821d others(5): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678407 | |||||||
| chr9:97678429 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.674-2842T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678429 | |||||||
| chr9:97678550 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.674-2963T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678550 | |||||||
| chr9:97678572 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.674-2985C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678572 | |||||||
| chr9:97678777 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.674-3190A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97678777 | |||||||
| chr9:97679025 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.674-3438C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679025 | |||||||
| chr9:97679117 | C | A | 1 | a0001c0001t0004g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.674-3530G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679117 | |||||||
| chr9:97679211 | G | T | 22 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0017 others(19): Show |
49 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.674-3624C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679211 | |||||||
| chr9:97679220 | T | C | 11 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(8): Show |
40 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.674-3633A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679220 | |||||||
| chr9:97679393 | A | AT | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-3807dupA | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679393 | |||||||
| chr9:97679431 | C | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-3844G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679431 | |||||||
| chr9:97679550 | T | TA | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.674-3964dupT | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679550 | |||||||
| chr9:97679835 | C | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-4248G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679835 | |||||||
| chr9:97679854 | C | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-4267G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679854 | |||||||
| chr9:97679908 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.674-4321G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679908 | |||||||
| chr9:97679912 | C | A | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.674-4325G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679912 | |||||||
| chr9:97679976 | T | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.674-4389A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97679976 | |||||||
| chr9:97680049 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.674-4462G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680049 | |||||||
| chr9:97680242 | C | T | 1 | a0001c0001t0003g0046 | 2 | NA18947.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.674-4655G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680242 | |||||||
| chr9:97680356 | A | C | 1 | a0001c0001t0002g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.673+4567T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680356 | |||||||
| chr9:97680387 | G | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(71): Show |
169 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.673+4536C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680387 | |||||||
| chr9:97680388 | T | A | 1 | a0001c0001t0004g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.673+4535A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680388 | |||||||
| chr9:97680524 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(156): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.673+4399A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680524 | |||||||
| chr9:97680598 | T | C | 3 | a0001c0001t0003g0121 a0002c0002t0003g0024 a0002c0002t0003g0120 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+4325A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680598 | |||||||
| chr9:97680764 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.673+4159C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680764 | |||||||
| chr9:97680780 | A | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0041 a0001c0001t0005g0106 others(3): Show |
12 | HG01891.hp2 HG01952.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.673+4143T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680780 | |||||||
| chr9:97680844 | C | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+4079G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97680844 | |||||||
| chr9:97681223 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.673+3700G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681223 | |||||||
| chr9:97681368 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.673+3555A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681368 | |||||||
| chr9:97681398 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+3525G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681398 | |||||||
| chr9:97681480 | C | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+3443G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681480 | |||||||
| chr9:97681663 | C | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+3260G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681663 | |||||||
| chr9:97681750 | T | A | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+3173A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681750 | |||||||
| chr9:97681771 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.673+3152A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681771 | |||||||
| chr9:97681793 | G | A | 1 | a0001c0001t0007g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.673+3130C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681793 | |||||||
| chr9:97681926 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.673+2997C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681926 | |||||||
| chr9:97681955 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.673+2968A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681955 | |||||||
| chr9:97681977 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.673+2946T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97681977 | |||||||
| chr9:97682062 | TTATC | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.673+2857_673+2860d others(6): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682062 | |||||||
| chr9:97682062 | TTATCTAT others(1): Show |
T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+2853_673+2860d others(10): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682062 | |||||||
| chr9:97682154 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.673+2769T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682154 | |||||||
| chr9:97682251 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.673+2672T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682251 | |||||||
| chr9:97682319 | C | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0146 |
3 | HG00673.hp1 HG02155.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.673+2604G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682319 | |||||||
| chr9:97682353 | G | C | 1 | a0001c0001t0002g0135 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.673+2570C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682353 | |||||||
| chr9:97682541 | T | C | 4 | a0001c0001t0004g0007 a0001c0001t0004g0044 a0001c0001t0004g0118 others(1): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.673+2382A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682541 | |||||||
| chr9:97682545 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.673+2378G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682545 | |||||||
| chr9:97682633 | C | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+2290G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682633 | |||||||
| chr9:97682669 | C | G | 12 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0048 others(9): Show |
29 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.673+2254G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682669 | |||||||
| chr9:97682715 | A | G | 1 | a0001c0001t0003g0010 | 8 | HG00609.hp2 NA18962.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.673+2208T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682715 | |||||||
| chr9:97682969 | G | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+1954C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97682969 | |||||||
| chr9:97683086 | T | C | 1 | a0001c0001t0004g0042 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.673+1837A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683086 | |||||||
| chr9:97683204 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.673+1719C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683204 | |||||||
| chr9:97683206 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.673+1717G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683206 | |||||||
| chr9:97683524 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.673+1399A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683524 | |||||||
| chr9:97683561 | A | G | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.673+1362T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683561 | |||||||
| chr9:97683584 | T | A | 22 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0017 others(19): Show |
49 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.673+1339A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683584 | |||||||
| chr9:97683585 | A | T | 2 | a0001c0001t0002g0158 a0001c0001t0005g0106 |
2 | HG01074.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.673+1338T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683585 | |||||||
| chr9:97683685 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.673+1238C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683685 | |||||||
| chr9:97683699 | T | TCTTAA | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+1223_673+1224i others(7): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683699 | |||||||
| chr9:97683761 | G | C | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.673+1162C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683761 | |||||||
| chr9:97683837 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.673+1086A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683837 | |||||||
| chr9:97683850 | C | CCTTAT | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+1068_673+1072d others(7): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683850 | |||||||
| chr9:97683948 | T | A | 1 | a0001c0001t0005g0041 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.673+975A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683948 | |||||||
| chr9:97683955 | G | A | 10 | a0001c0001t0002g0060 a0001c0001t0002g0157 a0001c0001t0003g0004 others(7): Show |
37 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.673+968C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683955 | |||||||
| chr9:97683995 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0096 |
3 | NA18953.hp1 NA18963.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.673+928G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97683995 | |||||||
| chr9:97684002 | A | G | 1 | a0001c0001t0001g0028 | 3 | HG00558.hp2 NA18953.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.673+921T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684002 | |||||||
| chr9:97684058 | CTT | C | 6 | a0001c0001t0005g0015 a0001c0001t0005g0041 a0001c0001t0005g0106 others(3): Show |
12 | HG01891.hp2 HG01952.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.673+863_673+864del others(2): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684058 | |||||||
| chr9:97684106 | A | C | 1 | a0001c0001t0003g0123 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.673+817T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684106 | |||||||
| chr9:97684243 | T | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+680A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684243 | |||||||
| chr9:97684246 | T | TGATG | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.673+673_673+676dup others(4): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684246 | |||||||
| chr9:97684374 | A | G | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.673+549T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684374 | |||||||
| chr9:97684391 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0073 |
3 | HG03831.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.673+532T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684391 | |||||||
| chr9:97684424 | G | C | 3 | a0001c0001t0003g0121 a0002c0002t0003g0024 a0002c0002t0003g0120 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+499C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684424 | |||||||
| chr9:97684439 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.673+484T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684439 | |||||||
| chr9:97684451 | A | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.673+472T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 5/5 | chr9 | 97684451 | |||||||
| chr9:97685072 | G | A | 3 | a0001c0001t0003g0121 a0002c0002t0003g0024 a0002c0002t0003g0120 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-32C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685072 | |||||||
| chr9:97685134 | T | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01069.hp2 HG01106.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.556-94A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685134 | |||||||
| chr9:97685195 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0082 |
22 | HG00423.hp2 HG01346.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.556-155T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685195 | |||||||
| chr9:97685504 | C | A | 1 | a0001c0001t0002g0052 | 2 | HG00408.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.556-464G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685504 | |||||||
| chr9:97685514 | T | A | 23 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0016 others(20): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.556-474A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685514 | |||||||
| chr9:97685579 | A | C | 2 | a0001c0001t0004g0115 a0003c0006t0004g0116 |
2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.556-539T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685579 | |||||||
| chr9:97685692 | A | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.556-652T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685692 | |||||||
| chr9:97685803 | A | G | 3 | a0001c0001t0002g0025 a0001c0001t0002g0050 a0001c0001t0002g0131 |
7 | HG01109.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-763T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685803 | |||||||
| chr9:97685890 | T | C | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.556-850A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685890 | |||||||
| chr9:97685925 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.556-885T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685925 | |||||||
| chr9:97685946 | C | T | 1 | a0001c0001t0002g0059 | 2 | HG01081.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.556-906G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97685946 | |||||||
| chr9:97686003 | A | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.556-963T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686003 | |||||||
| chr9:97686147 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.555+949A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686147 | |||||||
| chr9:97686335 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0062 |
3 | HG00140.hp1 HG00738.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.555+761T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686335 | |||||||
| chr9:97686386 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.555+710C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686386 | |||||||
| chr9:97686471 | T | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.555+625A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686471 | |||||||
| chr9:97686636 | G | A | 1 | a0001c0001t0002g0056 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.555+460C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686636 | |||||||
| chr9:97686662 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.555+434G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686662 | |||||||
| chr9:97686725 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0080 |
4 | HG02056.hp1 HG02129.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+371C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686725 | |||||||
| chr9:97686914 | AAAG | A | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.555+179_555+181del others(3): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 4/5 | chr9 | 97686914 | |||||||
| chr9:97687332 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.390-71T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97687332 | |||||||
| chr9:97687378 | T | C | 4 | a0001c0001t0004g0007 a0001c0001t0004g0044 a0001c0001t0004g0118 others(1): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.390-117A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97687378 | |||||||
| chr9:97687615 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.390-354C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97687615 | |||||||
| chr9:97687714 | C | T | 2 | a0001c0001t0003g0121 a0002c0002t0003g0024 |
5 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-453G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97687714 | |||||||
| chr9:97687756 | G | A | 33 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(30): Show |
82 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.390-495C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97687756 | |||||||
| chr9:97687868 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.390-607T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97687868 | |||||||
| chr9:97688081 | G | A | 1 | a0001c0001t0005g0031 | 3 | HG02976.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.390-820C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688081 | |||||||
| chr9:97688113 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.390-852T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688113 | |||||||
| chr9:97688293 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.390-1032G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688293 | |||||||
| chr9:97688334 | CACTT | C | 1 | a0001c0001t0002g0016 | 6 | HG01106.hp2 HG01516.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-1077_390-1074d others(6): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688334 | |||||||
| chr9:97688450 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.389+1084C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688450 | |||||||
| chr9:97688458 | T | C | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.389+1076A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688458 | |||||||
| chr9:97688669 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0102 |
5 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+865T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688669 | |||||||
| chr9:97688705 | T | C | 3 | a0001c0001t0003g0121 a0002c0002t0003g0024 a0002c0002t0003g0120 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+829A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688705 | |||||||
| chr9:97688705 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.389+829A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688705 | |||||||
| chr9:97688808 | A | T | 1 | a0001c0001t0002g0051 | 2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.389+726T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688808 | |||||||
| chr9:97688813 | G | GAA | 7 | a0001c0001t0005g0015 a0001c0001t0005g0031 a0001c0001t0005g0041 others(4): Show |
15 | HG01891.hp2 HG01952.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+719_389+720dup others(2): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688813 | |||||||
| chr9:97688914 | A | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.389+620T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688914 | |||||||
| chr9:97688957 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.389+577C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97688957 | |||||||
| chr9:97689225 | G | C | 1 | a0001c0001t0002g0053 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.389+309C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97689225 | |||||||
| chr9:97689228 | T | C | 1 | a0001c0001t0005g0031 | 3 | HG02976.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.389+306A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97689228 | |||||||
| chr9:97689274 | A | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.389+260T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 3/5 | chr9 | 97689274 | |||||||
| chr9:97689784 | T | TAA | 27 | a0001c0001t0003g0121 a0001c0001t0003g0124 a0001c0001t0004g0007 others(24): Show |
50 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.284-147_284-146dup others(2): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97689784 | |||||||
| chr9:97689784 | T | TTA | 6 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(3): Show |
32 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.284-146_284-145ins others(2): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97689784 | |||||||
| chr9:97689836 | A | AACGTAGC others(66): Show |
1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.284-270_284-198dup others(73): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97689836 | |||||||
| chr9:97689859 | T | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.284-220A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97689859 | |||||||
| chr9:97689866 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.284-227G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97689866 | |||||||
| chr9:97690153 | C | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.284-514G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690153 | |||||||
| chr9:97690273 | C | T | 1 | a0001c0001t0002g0032 | 3 | HG00597.hp2 NA18984.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.284-634G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690273 | |||||||
| chr9:97690419 | G | A | 1 | a0001c0001t0002g0054 | 2 | HG00544.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.284-780C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690419 | |||||||
| chr9:97690517 | AGCTGGGA others(126): Show |
A | 1 | a0001c0001t0001g0018 | 5 | NA18940.hp2 NA19076.hp2 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-1011_284-879de others(1): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690517 | |||||||
| chr9:97690538 | C | G | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-899G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690538 | |||||||
| chr9:97690598 | G | T | 22 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0017 others(19): Show |
49 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.284-959C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690598 | |||||||
| chr9:97690608 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.284-969C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690608 | |||||||
| chr9:97690608 | G | T | 1 | a0001c0001t0002g0009 | 4 | HG01358.hp1 HG01515.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-969C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690608 | |||||||
| chr9:97690780 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.284-1141G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690780 | |||||||
| chr9:97690788 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(97): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.284-1149C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690788 | |||||||
| chr9:97690818 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(97): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.284-1179G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690818 | |||||||
| chr9:97690910 | C | T | 1 | a0001c0001t0005g0031 | 3 | HG02976.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.284-1271G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690910 | |||||||
| chr9:97690941 | T | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.284-1302A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97690941 | |||||||
| chr9:97691016 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284-1377G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691016 | |||||||
| chr9:97691036 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0007g0076 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.284-1397T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691036 | |||||||
| chr9:97691209 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.284-1570T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691209 | |||||||
| chr9:97691288 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
6 | HG00673.hp2 NA18747.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1649G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691288 | |||||||
| chr9:97691321 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.284-1682T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691321 | |||||||
| chr9:97691345 | ACTTCAAA others(3): Show |
A | 1 | a0001c0001t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.284-1716_284-1707d others(12): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691345 | |||||||
| chr9:97691453 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.284-1814C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691453 | |||||||
| chr9:97691462 | GAGGCCA | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0042 a0001c0001t0004g0044 others(4): Show |
17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-1829_284-1824d others(8): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691462 | |||||||
| chr9:97691581 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(132): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.284-1942T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691581 | |||||||
| chr9:97691628 | G | A | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.284-1989C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691628 | |||||||
| chr9:97691743 | C | G | 3 | a0001c0001t0004g0105 a0001c0001t0004g0112 a0001c0001t0004g0114 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.283+1906G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691743 | |||||||
| chr9:97691798 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1851C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691798 | |||||||
| chr9:97691800 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1849A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691800 | |||||||
| chr9:97691802 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1847C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691802 | |||||||
| chr9:97691803 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1846T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691803 | |||||||
| chr9:97691805 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1844G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691805 | |||||||
| chr9:97691806 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1843G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691806 | |||||||
| chr9:97691807 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1842G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691807 | |||||||
| chr9:97691809 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1840C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691809 | |||||||
| chr9:97691810 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1839C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691810 | |||||||
| chr9:97691812 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1837C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691812 | |||||||
| chr9:97691813 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1836C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691813 | |||||||
| chr9:97691815 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1834C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691815 | |||||||
| chr9:97691816 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1833C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691816 | |||||||
| chr9:97691817 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1832T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691817 | |||||||
| chr9:97691818 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1831C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691818 | |||||||
| chr9:97691819 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1830C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691819 | |||||||
| chr9:97691833 | A | C | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.283+1816T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691833 | |||||||
| chr9:97691886 | A | AAT | 11 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0027 others(8): Show |
28 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.283+1761_283+1762d others(4): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | A | AATAT | 8 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0001g0102 others(5): Show |
16 | HG01167.hp1 HG01169.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+1759_283+1762d others(6): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | A | AATATATA others(1): Show |
1 | a0001c0001t0001g0026 | 3 | NA18985.hp1 NA19011.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.283+1755_283+1762d others(10): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283+1763T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | AAT | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0030 others(42): Show |
108 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.283+1761_283+1762d others(4): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | AATAT | A | 12 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0050 others(9): Show |
25 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.283+1759_283+1762d others(6): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | AATATATA others(1): Show |
A | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.283+1755_283+1762d others(10): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691886 | AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0034 | 2 | HG00438.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.283+1749_283+1762d others(16): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691886 | |||||||
| chr9:97691892 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.283+1757A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691892 | |||||||
| chr9:97691898 | T | A | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.283+1751A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691898 | |||||||
| chr9:97691902 | T | A | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.283+1747A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691902 | |||||||
| chr9:97691906 | T | A | 21 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(18): Show |
41 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.283+1743A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691906 | |||||||
| chr9:97691917 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1732C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691917 | |||||||
| chr9:97691919 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1730T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691919 | |||||||
| chr9:97691925 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1724T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691925 | |||||||
| chr9:97691926 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1723A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691926 | |||||||
| chr9:97691929 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1720T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691929 | |||||||
| chr9:97691930 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1719A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691930 | |||||||
| chr9:97691937 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1712T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691937 | |||||||
| chr9:97691948 | A | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0059 others(7): Show |
22 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+1701T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97691948 | |||||||
| chr9:97692000 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1649T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692000 | |||||||
| chr9:97692002 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1647C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692002 | |||||||
| chr9:97692011 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1638C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692011 | |||||||
| chr9:97692013 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1636G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692013 | |||||||
| chr9:97692015 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1634T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692015 | |||||||
| chr9:97692016 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1633C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692016 | |||||||
| chr9:97692017 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1632C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692017 | |||||||
| chr9:97692018 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1631A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692018 | |||||||
| chr9:97692020 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1629G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692020 | |||||||
| chr9:97692031 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1618C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692031 | |||||||
| chr9:97692032 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1617G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692032 | |||||||
| chr9:97692061 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283+1588C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692061 | |||||||
| chr9:97692066 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1583C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692066 | |||||||
| chr9:97692067 | T | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1582A>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692067 | |||||||
| chr9:97692069 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1580C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692069 | |||||||
| chr9:97692078 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1571T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692078 | |||||||
| chr9:97692088 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1561G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692088 | |||||||
| chr9:97692114 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1535T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692114 | |||||||
| chr9:97692147 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1502A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692147 | |||||||
| chr9:97692184 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1465C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692184 | |||||||
| chr9:97692212 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1437T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692212 | |||||||
| chr9:97692227 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1422C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692227 | |||||||
| chr9:97692229 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1420A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692229 | |||||||
| chr9:97692231 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1418G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692231 | |||||||
| chr9:97692234 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1415A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692234 | |||||||
| chr9:97692237 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1412C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692237 | |||||||
| chr9:97692238 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1411G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692238 | |||||||
| chr9:97692249 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1400G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692249 | |||||||
| chr9:97692254 | A | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.283+1395T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692254 | |||||||
| chr9:97692256 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1393T>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692256 | |||||||
| chr9:97692258 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1391A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692258 | |||||||
| chr9:97692259 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1390G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692259 | |||||||
| chr9:97692262 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1387C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692262 | |||||||
| chr9:97692264 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1385G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692264 | |||||||
| chr9:97692294 | AGAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1343_283+1354d others(14): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692294 | |||||||
| chr9:97692310 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1339T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692310 | |||||||
| chr9:97692312 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1337C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692312 | |||||||
| chr9:97692315 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1334T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692315 | |||||||
| chr9:97692316 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1333T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692316 | |||||||
| chr9:97692317 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1332A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692317 | |||||||
| chr9:97692319 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1330C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692319 | |||||||
| chr9:97692323 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1326A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692323 | |||||||
| chr9:97692327 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1322C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692327 | |||||||
| chr9:97692328 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1321A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692328 | |||||||
| chr9:97692331 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1318A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692331 | |||||||
| chr9:97692336 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1313A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692336 | |||||||
| chr9:97692337 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1312C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692337 | |||||||
| chr9:97692338 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1311A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692338 | |||||||
| chr9:97692340 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1309A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692340 | |||||||
| chr9:97692341 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1308C>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692341 | |||||||
| chr9:97692385 | A | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0050 a0001c0001t0002g0131 others(1): Show |
8 | HG01109.hp2 HG01243.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+1264T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692385 | |||||||
| chr9:97692481 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1168T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692481 | |||||||
| chr9:97692517 | AAAGTGGT others(3): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.283+1122_283+1131d others(12): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692517 | |||||||
| chr9:97692771 | A | G | 3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0126 |
5 | HG02257.hp2 HG02280.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+878T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692771 | |||||||
| chr9:97692811 | C | T | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.283+838G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692811 | |||||||
| chr9:97692820 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.283+829C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97692820 | |||||||
| chr9:97693050 | C | CT | 5 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0130 others(2): Show |
7 | HG00423.hp1 HG01168.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+598dupA | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693050 | |||||||
| chr9:97693050 | CT | C | 22 | a0001c0001t0001g0097 a0001c0001t0002g0057 a0001c0001t0002g0058 others(19): Show |
55 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.283+598delA | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693050 | |||||||
| chr9:97693066 | T | A | 31 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(28): Show |
80 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.283+583A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693066 | |||||||
| chr9:97693066 | T | TA | 3 | a0001c0001t0004g0104 a0001c0001t0004g0110 a0001c0001t0004g0111 |
3 | HG02630.hp2 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+582dupT | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693066 | |||||||
| chr9:97693072 | AAAG | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0038 others(4): Show |
18 | HG00639.hp2 HG01496.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.283+574_283+576del others(3): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693072 | |||||||
| chr9:97693081 | AT | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0059 others(7): Show |
22 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+567delA | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693081 | |||||||
| chr9:97693108 | T | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0044 a0001c0001t0004g0118 others(1): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+541A>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693108 | |||||||
| chr9:97693260 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.283+389C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693260 | |||||||
| chr9:97693623 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.283+26T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 2/5 | chr9 | 97693623 | |||||||
| chr9:97694082 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18995.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.173-323G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694082 | |||||||
| chr9:97694127 | G | A | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.173-368C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694127 | |||||||
| chr9:97694178 | A | G | 4 | a0001c0001t0004g0007 a0001c0001t0004g0044 a0001c0001t0004g0118 others(1): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.173-419T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694178 | |||||||
| chr9:97694251 | TGTGC | T | 1 | a0001c0001t0002g0020 | 5 | HG00642.hp2 HG01074.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-496_173-493del others(4): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694251 | |||||||
| chr9:97694256 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0044 a0001c0001t0004g0118 others(1): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.173-497C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694256 | |||||||
| chr9:97694315 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 |
6 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.173-556C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694315 | |||||||
| chr9:97694479 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.173-720C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694479 | |||||||
| chr9:97694778 | G | T | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.173-1019C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694778 | |||||||
| chr9:97694795 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.173-1036G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694795 | |||||||
| chr9:97694838 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.173-1079T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694838 | |||||||
| chr9:97694851 | C | A | 1 | a0001c0001t0005g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.173-1092G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97694851 | |||||||
| chr9:97695148 | G | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.173-1389C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695148 | |||||||
| chr9:97695173 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.173-1414A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695173 | |||||||
| chr9:97695223 | T | TTAAAA | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.173-1465_173-1464i others(7): Show |
XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695223 | |||||||
| chr9:97695452 | T | C | 8 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(5): Show |
34 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.172+1669A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695452 | |||||||
| chr9:97695477 | A | G | 7 | a0001c0001t0005g0015 a0001c0001t0005g0031 a0001c0001t0005g0041 others(4): Show |
15 | HG01891.hp2 HG01952.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.172+1644T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695477 | |||||||
| chr9:97695535 | G | T | 1 | a0001c0001t0002g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172+1586C>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695535 | |||||||
| chr9:97695558 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.172+1563C>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695558 | |||||||
| chr9:97695788 | A | C | 1 | a0001c0001t0002g0047 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172+1333T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695788 | |||||||
| chr9:97695790 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172+1331G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695790 | |||||||
| chr9:97695827 | C | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0059 others(7): Show |
22 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.172+1294G>T | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695827 | |||||||
| chr9:97695900 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0104 |
3 | HG03225.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.172+1221G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97695900 | |||||||
| chr9:97696018 | T | C | 1 | a0001c0001t0006g0043 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.172+1103A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696018 | |||||||
| chr9:97696058 | A | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.172+1063T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696058 | |||||||
| chr9:97696281 | C | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.172+840G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696281 | |||||||
| chr9:97696418 | A | G | 1 | a0001c0001t0003g0119 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.172+703T>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696418 | |||||||
| chr9:97696537 | T | C | 4 | a0001c0001t0004g0007 a0001c0001t0004g0044 a0001c0001t0004g0118 others(1): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.172+584A>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696537 | |||||||
| chr9:97696766 | C | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0042 others(20): Show |
43 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.172+355G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696766 | |||||||
| chr9:97696771 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.172+350G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696771 | |||||||
| chr9:97696917 | A | C | 34 | a0001c0001t0003g0004 a0001c0001t0003g0010 a0001c0001t0003g0045 others(31): Show |
83 | HG00597.hp1 HG00609.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.172+204T>G | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696917 | |||||||
| chr9:97696999 | C | G | 1 | a0001c0001t0004g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.172+122G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97696999 | |||||||
| chr9:97697027 | C | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
20 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.172+94G>C | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97697027 | |||||||
| chr9:97697062 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0104 |
3 | HG03225.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.172+59G>A | XPA | ENSG00000136936.11 | transcript | ENST00000375128.5 | protein_coding | 1/5 | chr9 | 97697062 |