Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 389668 |
| ensemblid | ENSG00000221947.8 |
| hgncid | 20937 |
| symbol | XKR9 |
| name | XK related 9 |
| refseq_nuc | NM_001011720.2 |
| refseq_prot | NP_001011720.1 |
| ensembl_nuc | ENST00000408926.8 |
| ensembl_prot | ENSP00000386141.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 70669339 |
| end | 70735942 |
| strand | + |
| ver | v1.2 |
| region | chr8:70669339-70735942 |
| region5000 | chr8:70664339-70740942 |
| regionname0 | XKR9_chr8_70669339_70735942 |
| regionname5000 | XKR9_chr8_70664339_70740942 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 373 | 313 | 80 | 57 | 136 | 10 | 28 | 110 | XKR9_chr8_70664339_70740942 | XKR9 | MKYTK others(368): Show |
chr8 | 70664339 | 70740942 |
| a0002 | 0/0 | 373 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | MKYTK others(368): Show |
chr8 | 70664339 | 70740942 |
| a0003 | 0/0 | 182 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | MKYTK others(177): Show |
chr8 | 70664339 | 70740942 |
| a0004 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | MKYTK others(368): Show |
chr8 | 70664339 | 70740942 |
| a0005 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | MKYTK others(368): Show |
chr8 | 70664339 | 70740942 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1119 | 212 | 54 | 37 | 98 | 5 | 17 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0001c0002 | 0/1 | 1119 | 86 | 22 | 19 | 31 | 4 | 9 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0001c0003 | 0/0 | 1119 | 7 | 0 | 0 | 7 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0001c0005 | 0/0 | 1119 | 4 | 0 | 1 | 0 | 1 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0001c0006 | 0/0 | 1119 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0002c0004 | 0/0 | 1119 | 5 | 5 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0003c0007 | 0/0 | 1119 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0004c0008 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 | ||
| a0005c0009 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | ATGAA others(1114): Show |
chr8 | 70664339 | 70740942 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3200 | 106 | 22 | 13 | 54 | 4 | 12 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0003 | 0/0 | 3200 | 50 | 0 | 12 | 36 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0004 | 0/0 | 3200 | 35 | 19 | 11 | 1 | 1 | 3 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0006 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0007 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0010 | 0/0 | 3196 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3191): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0011 | 0/0 | 3200 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0012 | 0/0 | 3196 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3191): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0013 | 0/0 | 3200 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0014 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0015 | 0/0 | 3193 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3188): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0016 | 0/0 | 3197 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3192): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0017 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0018 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0019 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0020 | 0/0 | 3199 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3194): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0021 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0001t0025 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0002t0002 | 0/1 | 3200 | 70 | 14 | 13 | 31 | 4 | 7 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0002t0005 | 0/0 | 3200 | 9 | 2 | 5 | 0 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0002t0008 | 0/0 | 3197 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3192): Show |
chr8 | 70664339 | 70740942 |
| a0001c0002t0022 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0002t0023 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0002t0024 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0003t0003 | 0/0 | 3200 | 7 | 0 | 0 | 7 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0005t0006 | 0/0 | 3200 | 4 | 0 | 1 | 0 | 1 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0001c0006t0007 | 0/0 | 3200 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0002c0004t0002 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0002c0004t0009 | 0/0 | 3199 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3194): Show |
chr8 | 70664339 | 70740942 |
| a0003c0007t0001 | 0/0 | 3200 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0004c0008t0002 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| a0005c0009t0004 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | AGAGG others(3195): Show |
chr8 | 70664339 | 70740942 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0012g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0014g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0015g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0017g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0020g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0001t0025g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0002g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0022g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0023g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0002t0024g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0005t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0005t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0005t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0005t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0006t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0001c0006t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0002c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0002c0004t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0002c0004t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0002c0004t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0002c0004t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0003c0007t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0003c0007t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0004c0008t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| a0005c0009t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0006 | g0089 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0013 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0271 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00639 | hp2 | a0001 | c0005 | t0006 | g0090 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00642 | hp1 | a0001 | c0002 | t0005 | g0210 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0272 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01074 | hp2 | a0001 | c0002 | t0005 | g0213 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0233 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0023 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0023 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01256 | hp1 | a0004 | c0008 | t0002 | g0010 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01258 | hp2 | a0001 | c0002 | t0024 | g0273 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0270 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0274 | EUR | IBS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02004 | hp1 | a0001 | c0002 | t0005 | g0209 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0196 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02056 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02074 | hp2 | a0001 | c0001 | t0014 | g0052 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0116 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02135 | hp1 | a0001 | c0001 | t0021 | g0084 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02148 | hp1 | a0001 | c0001 | t0025 | g0007 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0065 | EAS | CDX | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02258 | hp1 | a0001 | c0002 | t0023 | g0228 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0263 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02451 | hp1 | a0001 | c0006 | t0007 | g0008 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0110 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0111 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02615 | hp2 | a0001 | c0006 | t0007 | g0008 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0046 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0245 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02717 | hp1 | a0001 | c0002 | t0022 | g0239 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02735 | hp1 | a0001 | c0005 | t0006 | g0115 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0246 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02738 | hp2 | a0001 | c0002 | t0005 | g0212 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0094 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02897 | hp2 | a0001 | c0006 | t0007 | g0080 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0113 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0250 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02970 | hp2 | a0001 | c0006 | t0007 | g0008 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0112 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0275 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0227 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0215 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0243 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0078 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03209 | hp1 | a0002 | c0004 | t0009 | g0218 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0244 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03453 | hp2 | a0002 | c0004 | t0009 | g0216 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0107 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0214 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03516 | hp1 | a0002 | c0004 | t0009 | g0217 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03516 | hp2 | a0001 | c0002 | t0008 | g0249 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0194 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03704 | hp1 | a0001 | c0005 | t0006 | g0093 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18522 | hp1 | a0005 | c0009 | t0004 | g0079 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18522 | hp2 | a0002 | c0004 | t0002 | g0238 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CHB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0230 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18952 | hp1 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18952 | hp2 | a0001 | c0001 | t0020 | g0124 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18968 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18981 | hp2 | a0001 | c0003 | t0003 | g0076 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18982 | hp2 | a0001 | c0001 | t0019 | g0147 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18991 | hp2 | a0001 | c0001 | t0011 | g0127 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18993 | hp2 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0211 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19062 | hp1 | a0003 | c0007 | t0001 | g0143 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0058 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0060 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19084 | hp2 | a0003 | c0007 | t0001 | g0148 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0235 | AFR | ASW | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ASW | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0229 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG03471 | hp2 | a0001 | c0002 | t0008 | g0251 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0031 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA20300 | hp2 | a0002 | c0004 | t0009 | g0219 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0279 | REF | REF | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0088 | REF | REF | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70707000 | G | T | 1 | a0002 | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.340G>T | p.Val114Leu | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/5 | 900/3200 | 340/1122 | 114/373 | chr8 | 70707000 | |||
| chr8:70707037 | A | G | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.377A>G | p.Asp126Gly | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/5 | 937/3200 | 377/1122 | 126/373 | chr8 | 70707037 | |||
| chr8:70733849 | C | T | 1 | a0003 | 2 | NA19062.hp1 NA19084.hp2 |
stop_gained | HIGH | c.547C>T | p.Gln183* | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1107/3200 | 547/1122 | 183/373 | chr8 | 70733849 | |||
| chr8:70733877 | A | T | 1 | a0004 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.575A>T | p.Asp192Val | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1135/3200 | 575/1122 | 192/373 | chr8 | 70733877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70681190 | G | A | 3 | a0001c0002 a0002c0004 a0004c0008 |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
synonymous_variant | LOW | c.132G>A | p.Ala44Ala | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 692/3200 | 132/1122 | 44/373 | chr8 | 70681190 | |||
| chr8:70707018 | C | T | 1 | a0001c0006 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.358C>T | p.Leu120Leu | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/5 | 918/3200 | 358/1122 | 120/373 | chr8 | 70707018 | |||
| chr8:70734226 | C | T | 1 | a0001c0005 | 4 | HG00099.hp1 HG00639.hp2 HG02735.hp1 others(1): Show |
synonymous_variant | LOW | c.924C>T | p.Cys308Cys | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1484/3200 | 924/1122 | 308/373 | chr8 | 70734226 | |||
| chr8:70734241 | T | C | 1 | a0001c0003 | 7 | HG02056.hp2 HG02165.hp2 NA18968.hp1 others(4): Show |
synonymous_variant | LOW | c.939T>C | p.Phe313Phe | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1499/3200 | 939/1122 | 313/373 | chr8 | 70734241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70680840 | A | G | 1 | a0001c0001t0025 | 1 | HG02148.hp1 | 5_prime_UTR_variant | MODIFIER | c.-219A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 219 | chr8 | 70680840 | ||||||
| chr8:70680929 | C | T | 1 | a0001c0002t0024 | 1 | HG01258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 130 | chr8 | 70680929 | ||||||
| chr8:70680963 | A | G | 7 | a0001c0002t0002 a0001c0002t0022 a0001c0002t0023 others(4): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-96A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 96 | chr8 | 70680963 | ||||||
| chr8:70734442 | T | C | 1 | a0001c0001t0014 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 18 | chr8 | 70734442 | ||||||
| chr8:70734445 | A | G | 1 | a0001c0002t0023 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 21 | chr8 | 70734445 | ||||||
| chr8:70734606 | A | T | 1 | a0001c0001t0021 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 182 | chr8 | 70734606 | ||||||
| chr8:70734651 | TC | T | 1 | a0002c0004t0009 | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*228delC | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 228 | chr8 | 70734651 | ||||||
| chr8:70734673 | A | G | 1 | a0001c0001t0013 | 2 | HG02895.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*249A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 249 | chr8 | 70734673 | ||||||
| chr8:70734745 | T | C | 7 | a0001c0002t0002 a0001c0002t0022 a0001c0002t0023 others(4): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 321 | chr8 | 70734745 | ||||||
| chr8:70734974 | G | GACCTCTC others(11): Show |
1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552_*553insCTCTCA others(12): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 553 | INFO_REALIGN_3_PRIME | chr8 | 70734974 | |||||
| chr8:70734982 | A | T | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 558 | chr8 | 70734982 | ||||||
| chr8:70734986 | T | C | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*562T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 562 | chr8 | 70734986 | ||||||
| chr8:70734992 | T | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 568 | chr8 | 70734992 | ||||||
| chr8:70734994 | T | A | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 570 | chr8 | 70734994 | ||||||
| chr8:70734998 | C | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*574C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 574 | chr8 | 70734998 | ||||||
| chr8:70734999 | T | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 575 | chr8 | 70734999 | ||||||
| chr8:70735010 | A | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*586A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 586 | chr8 | 70735010 | ||||||
| chr8:70735016 | T | A | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 592 | chr8 | 70735016 | ||||||
| chr8:70735023 | T | C | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 599 | chr8 | 70735023 | ||||||
| chr8:70735026 | A | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*602A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 602 | chr8 | 70735026 | ||||||
| chr8:70735029 | T | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 605 | chr8 | 70735029 | ||||||
| chr8:70735030 | ATAATTAT others(12): Show |
A | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*608_*626delAATTAT others(13): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 608 | INFO_REALIGN_3_PRIME | chr8 | 70735030 | |||||
| chr8:70735051 | G | T | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*627G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 627 | chr8 | 70735051 | ||||||
| chr8:70735125 | A | G | 2 | a0001c0002t0005 a0001c0002t0008 |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*701A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 701 | chr8 | 70735125 | ||||||
| chr8:70735202 | G | A | 1 | a0001c0002t0005 | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*778G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 778 | chr8 | 70735202 | ||||||
| chr8:70735204 | C | A | 1 | a0001c0002t0022 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 780 | chr8 | 70735204 | ||||||
| chr8:70735232 | CTATT | C | 3 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 |
6 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*813_*816delTATT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 813 | INFO_REALIGN_3_PRIME | chr8 | 70735232 | |||||
| chr8:70735364 | A | T | 1 | a0001c0001t0019 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*940A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 940 | chr8 | 70735364 | ||||||
| chr8:70735370 | G | T | 26 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(23): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*946G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 946 | chr8 | 70735370 | ||||||
| chr8:70735459 | ATAT | A | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0002t0008 |
6 | HG02965.hp2 HG03098.hp2 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1054_*1056delTAT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1054 | INFO_REALIGN_3_PRIME | chr8 | 70735459 | |||||
| chr8:70735578 | T | G | 2 | a0001c0002t0005 a0001c0002t0008 |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1154T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1154 | chr8 | 70735578 | ||||||
| chr8:70735620 | C | A | 2 | a0001c0001t0011 a0001c0001t0021 |
4 | HG02132.hp1 HG02135.hp1 NA18952.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1196C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1196 | chr8 | 70735620 | ||||||
| chr8:70735641 | G | T | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1217 | chr8 | 70735641 | ||||||
| chr8:70735679 | G | A | 4 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0025 others(1): Show |
59 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1255G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1255 | chr8 | 70735679 | ||||||
| chr8:70735731 | G | A | 3 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 |
6 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1307 | chr8 | 70735731 | ||||||
| chr8:70735830 | A | C | 2 | a0001c0001t0016 a0001c0001t0017 |
2 | HG03195.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1406A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1406 | chr8 | 70735830 | ||||||
| chr8:70735861 | T | C | 1 | a0001c0001t0010 | 3 | HG02451.hp2 HG02965.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1437T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1437 | chr8 | 70735861 | ||||||
| chr8:70735912 | T | C | 5 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0016 others(2): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1488T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1488 | chr8 | 70735912 | ||||||
| chr8:70735933 | T | C | 2 | a0001c0001t0006 a0001c0005t0006 |
5 | HG00099.hp1 HG00639.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1509T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1509 | chr8 | 70735933 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70669606 | C | CTG | 2 | a0001c0001t0003g0028 a0001c0001t0003g0278 |
3 | HG00735.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-361+100_-361+101d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669606 | ||||||
| chr8:70669606 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0003g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-361+92_-361+101de others(11): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669606 | ||||||
| chr8:70669606 | CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0006g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-361+88_-361+101de others(15): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669606 | ||||||
| chr8:70669635 | TGTGTA | T | 17 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0032 others(14): Show |
19 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-361+100_-361+104d others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669635 | ||||||
| chr8:70669637 | TGTA | T | 88 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(85): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-361+116_-361+118d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669637 | ||||||
| chr8:70669639 | T | TG | 28 | a0001c0001t0001g0181 a0001c0001t0010g0110 a0001c0001t0010g0112 others(25): Show |
32 | HG00621.hp2 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | |||||||
| chr8:70669639 | T | TGTG | 9 | a0001c0002t0002g0004 a0001c0002t0002g0025 a0001c0002t0002g0026 others(6): Show |
11 | HG02738.hp2 HG02922.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | |||||||
| chr8:70669639 | T | TGTGTG | 7 | a0001c0001t0007g0114 a0001c0002t0002g0220 a0001c0002t0002g0222 others(4): Show |
7 | HG01256.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | |||||||
| chr8:70669639 | T | TGTGTGTG | 8 | a0001c0002t0002g0024 a0001c0002t0002g0221 a0001c0002t0002g0230 others(5): Show |
8 | HG01243.hp1 HG03209.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(9): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | |||||||
| chr8:70669639 | TA | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0120 others(38): Show |
44 | HG00673.hp2 HG01167.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.-361+102delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | |||||||
| chr8:70669640 | A | G | 31 | a0001c0002t0002g0011 a0001c0002t0002g0027 a0001c0002t0002g0252 others(28): Show |
34 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-361+102A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669640 | |||||||
| chr8:70669640 | A | T | 52 | a0001c0001t0001g0181 a0001c0001t0007g0114 a0001c0001t0010g0110 others(49): Show |
60 | HG00621.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.-361+102A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669640 | |||||||
| chr8:70669641 | G | T | 31 | a0001c0002t0002g0011 a0001c0002t0002g0027 a0001c0002t0002g0252 others(28): Show |
34 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-361+103G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669641 | |||||||
| chr8:70669642 | T | G | 31 | a0001c0002t0002g0011 a0001c0002t0002g0027 a0001c0002t0002g0252 others(28): Show |
34 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-361+104T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | |||||||
| chr8:70669642 | T | TG | 45 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0024 others(42): Show |
53 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.-361+104_-361+105i others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | |||||||
| chr8:70669642 | T | TGTGTGTG others(16): Show |
1 | a0001c0002t0002g0247 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-361+104_-361+105i others(25): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | |||||||
| chr8:70669642 | T | TGTGTGTG others(18): Show |
1 | a0001c0002t0002g0248 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-361+104_-361+105i others(27): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | |||||||
| chr8:70669643 | A | T | 78 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(75): Show |
89 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.-361+105A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669643 | |||||||
| chr8:70669664 | A | AT | 10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0045 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-361+146dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | ||||||
| chr8:70669664 | A | ATT | 100 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-361+145_-361+146d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | ||||||
| chr8:70669664 | AT | A | 98 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0006 others(95): Show |
117 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-361+146delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | ||||||
| chr8:70669664 | ATT | A | 10 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0047 others(7): Show |
15 | HG00735.hp1 HG01978.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.-361+145_-361+146d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | ||||||
| chr8:70669664 | ATTT | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-361+144_-361+146d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | ||||||
| chr8:70669747 | A | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-361+209A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669747 | |||||||
| chr8:70669774 | C | T | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-361+236C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669774 | |||||||
| chr8:70669956 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-361+418A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669956 | |||||||
| chr8:70670131 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-361+593A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670131 | |||||||
| chr8:70670244 | TGCCTGCC others(25): Show |
T | 1 | a0001c0001t0016g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-361+710_-361+741d others(34): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70670244 | ||||||
| chr8:70670355 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-361+817C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670355 | |||||||
| chr8:70670356 | A | C | 28 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(25): Show |
32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-361+818A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670356 | |||||||
| chr8:70670423 | C | T | 1 | a0001c0001t0013g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-361+885C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670423 | |||||||
| chr8:70670446 | T | C | 1 | a0001c0001t0011g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-361+908T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670446 | |||||||
| chr8:70670509 | CT | C | 12 | a0001c0002t0002g0240 a0001c0002t0002g0241 a0001c0002t0002g0242 others(9): Show |
12 | HG02630.hp1 HG02717.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-361+982delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70670509 | ||||||
| chr8:70670518 | T | A | 1 | a0001c0002t0005g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-361+980T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670518 | |||||||
| chr8:70670519 | T | A | 11 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(8): Show |
12 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-361+981T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670519 | |||||||
| chr8:70670519 | T | TA | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-361+981_-361+982i others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670519 | |||||||
| chr8:70670520 | T | A | 216 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(213): Show |
241 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-361+982T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670520 | |||||||
| chr8:70670528 | G | A | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.-361+990G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670528 | |||||||
| chr8:70670621 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18939.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-361+1083C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670621 | |||||||
| chr8:70670838 | T | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-361+1300T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670838 | |||||||
| chr8:70670843 | C | G | 3 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 |
3 | HG02630.hp1 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-361+1305C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670843 | |||||||
| chr8:70670861 | G | A | 2 | a0001c0002t0002g0247 a0001c0002t0002g0248 |
2 | HG01255.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-361+1323G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670861 | |||||||
| chr8:70671032 | T | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-361+1494T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671032 | |||||||
| chr8:70671075 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-361+1537G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671075 | |||||||
| chr8:70671288 | A | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0198 others(6): Show |
10 | HG02165.hp1 NA18612.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.-361+1750A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671288 | |||||||
| chr8:70671320 | CATGATCT others(1081): Show |
C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-361+1799_-360-239 others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671320 | ||||||
| chr8:70671329 | ATT | A | 63 | a0001c0001t0001g0146 a0001c0001t0001g0153 a0001c0001t0001g0195 others(60): Show |
79 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-361+1806_-361+180 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671329 | ||||||
| chr8:70671329 | ATTT | A | 130 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(127): Show |
138 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-361+1805_-361+180 others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671329 | ||||||
| chr8:70671329 | ATTTT | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0167 others(2): Show |
8 | HG01891.hp1 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-361+1804_-361+180 others(8): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671329 | ||||||
| chr8:70671394 | A | G | 1 | a0001c0001t0004g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-361+1856A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671394 | |||||||
| chr8:70671425 | T | C | 1 | a0001c0001t0013g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-361+1887T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671425 | |||||||
| chr8:70671557 | C | A | 2 | a0001c0001t0004g0012 a0001c0001t0004g0045 |
3 | HG02145.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-361+2019C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671557 | |||||||
| chr8:70671725 | A | G | 149 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(146): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-361+2187A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671725 | |||||||
| chr8:70671923 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-361+2385C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671923 | |||||||
| chr8:70672044 | A | G | 1 | a0001c0001t0020g0124 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-361+2506A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672044 | |||||||
| chr8:70672083 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0075 |
3 | NA18944.hp1 NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-361+2545T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672083 | |||||||
| chr8:70672125 | G | A | 4 | a0001c0001t0004g0015 a0001c0001t0004g0095 a0001c0001t0004g0096 others(1): Show |
5 | HG02055.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-361+2587G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672125 | |||||||
| chr8:70672256 | T | C | 1 | a0001c0001t0007g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-360-2562T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672256 | |||||||
| chr8:70672606 | C | CTG | 5 | a0001c0001t0001g0195 a0001c0001t0007g0114 a0001c0001t0013g0087 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-360-2194_-360-219 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70672606 | ||||||
| chr8:70672768 | AG | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0195 |
3 | HG03704.hp2 HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-360-2049delG | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672768 | |||||||
| chr8:70672933 | T | A | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-360-1885T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672933 | |||||||
| chr8:70672934 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-360-1884T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672934 | |||||||
| chr8:70673218 | G | C | 1 | a0001c0002t0008g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-360-1600G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673218 | |||||||
| chr8:70673374 | G | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-360-1444G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673374 | |||||||
| chr8:70673475 | G | A | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-360-1343G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673475 | |||||||
| chr8:70673524 | C | T | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-360-1294C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673524 | |||||||
| chr8:70673694 | G | A | 1 | a0001c0002t0002g0252 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-360-1124G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673694 | |||||||
| chr8:70673721 | C | T | 2 | a0001c0001t0007g0114 a0001c0001t0018g0196 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-360-1097C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673721 | |||||||
| chr8:70673824 | G | C | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.-360-994G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673824 | |||||||
| chr8:70673917 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-360-901G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673917 | |||||||
| chr8:70674348 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-360-470C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674348 | |||||||
| chr8:70674501 | T | A | 2 | a0001c0001t0007g0114 a0001c0001t0018g0196 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-360-317T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674501 | |||||||
| chr8:70674659 | C | A | 1 | a0001c0002t0002g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-360-159C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674659 | |||||||
| chr8:70674736 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-360-82A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674736 | |||||||
| chr8:70674908 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-279+9A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70674908 | |||||||
| chr8:70675012 | C | T | 4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-279+113C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675012 | |||||||
| chr8:70675025 | G | A | 1 | a0001c0001t0004g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-279+126G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675025 | |||||||
| chr8:70675041 | A | G | 5 | a0001c0001t0001g0086 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-279+142A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675041 | |||||||
| chr8:70675076 | G | A | 1 | a0001c0001t0014g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-279+177G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675076 | |||||||
| chr8:70675162 | C | T | 1 | a0001c0001t0006g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-279+263C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675162 | |||||||
| chr8:70675187 | G | A | 1 | a0001c0001t0001g0017 | 2 | NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-279+288G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675187 | |||||||
| chr8:70675235 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-279+336G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675235 | |||||||
| chr8:70675331 | G | T | 1 | a0001c0001t0003g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-279+432G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675331 | |||||||
| chr8:70675441 | C | T | 1 | a0001c0003t0003g0076 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-279+542C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675441 | |||||||
| chr8:70675458 | T | C | 1 | a0001c0001t0012g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-279+559T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675458 | |||||||
| chr8:70675474 | C | G | 2 | a0002c0004t0009g0217 a0002c0004t0009g0218 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-279+575C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675474 | |||||||
| chr8:70675666 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-279+767A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675666 | |||||||
| chr8:70675899 | T | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1000T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675899 | |||||||
| chr8:70675900 | T | G | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1001T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675900 | |||||||
| chr8:70675902 | C | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1003C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675902 | |||||||
| chr8:70675903 | T | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1004T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675903 | |||||||
| chr8:70676134 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-279+1235G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676134 | |||||||
| chr8:70676151 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-279+1252T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676151 | |||||||
| chr8:70676159 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-279+1260G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676159 | |||||||
| chr8:70676191 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-279+1292G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676191 | |||||||
| chr8:70676422 | G | A | 4 | a0001c0001t0004g0015 a0001c0001t0004g0095 a0001c0001t0004g0096 others(1): Show |
5 | HG02055.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-279+1523G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676422 | |||||||
| chr8:70676845 | TAAAC | T | 6 | a0001c0001t0001g0184 a0002c0004t0002g0238 a0002c0004t0009g0216 others(3): Show |
6 | HG01074.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-279+1965_-279+196 others(8): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70676845 | ||||||
| chr8:70676973 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+2074G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676973 | |||||||
| chr8:70677041 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-279+2142G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677041 | |||||||
| chr8:70677126 | T | TA | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-279+2236dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70677126 | ||||||
| chr8:70677126 | TA | T | 105 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-279+2236delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70677126 | ||||||
| chr8:70677171 | G | GGTCTCAC others(28): Show |
3 | a0001c0001t0004g0013 a0001c0001t0004g0042 a0001c0001t0004g0043 |
4 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-279+2274_-279+230 others(39): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70677171 | ||||||
| chr8:70677249 | G | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0075 |
3 | NA18944.hp1 NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-279+2350G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677249 | |||||||
| chr8:70677369 | A | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-279+2470A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677369 | |||||||
| chr8:70677414 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-279+2515C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677414 | |||||||
| chr8:70677790 | A | C | 1 | a0001c0001t0011g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-279+2891A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677790 | |||||||
| chr8:70677916 | A | G | 1 | a0001c0002t0002g0026 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-278-2865A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677916 | |||||||
| chr8:70678123 | C | T | 1 | a0001c0002t0008g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-278-2658C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678123 | |||||||
| chr8:70678208 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-278-2573T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678208 | |||||||
| chr8:70678369 | T | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-278-2412T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678369 | |||||||
| chr8:70678961 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-278-1820C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678961 | |||||||
| chr8:70678968 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-278-1813A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678968 | |||||||
| chr8:70679230 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-278-1551T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70679230 | |||||||
| chr8:70679559 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-278-1222C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70679559 | |||||||
| chr8:70680078 | G | A | 112 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(109): Show |
120 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-278-703G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70680078 | |||||||
| chr8:70680378 | A | G | 1 | a0001c0002t0002g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-278-403A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70680378 | |||||||
| chr8:70681428 | CTTA | C | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+101_272+103del others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70681428 | ||||||
| chr8:70681692 | A | C | 1 | a0001c0002t0002g0268 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.272+362A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681692 | |||||||
| chr8:70681787 | TTAAGAAT others(20): Show |
T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+458_272+484del others(27): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681787 | |||||||
| chr8:70681904 | A | G | 2 | a0001c0001t0004g0081 a0005c0009t0004g0079 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.272+574A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681904 | |||||||
| chr8:70681981 | T | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+651T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681981 | |||||||
| chr8:70682089 | T | C | 1 | a0001c0006t0007g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.272+759T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682089 | |||||||
| chr8:70682159 | T | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+829T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682159 | |||||||
| chr8:70682413 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.272+1083A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682413 | |||||||
| chr8:70682483 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+1153G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682483 | |||||||
| chr8:70682670 | CT | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+1342delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70682670 | ||||||
| chr8:70682812 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.272+1482A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682812 | |||||||
| chr8:70682824 | C | T | 118 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(115): Show |
126 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.272+1494C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682824 | |||||||
| chr8:70682985 | A | G | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+1655A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682985 | |||||||
| chr8:70682991 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+1661C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682991 | |||||||
| chr8:70683168 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(29): Show |
36 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.272+1838T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683168 | |||||||
| chr8:70683247 | T | A | 2 | a0001c0001t0004g0012 a0001c0001t0004g0045 |
3 | HG02145.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.272+1917T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683247 | |||||||
| chr8:70683300 | A | G | 1 | a0001c0001t0003g0074 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.272+1970A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683300 | |||||||
| chr8:70683475 | C | A | 1 | a0001c0001t0004g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.272+2145C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683475 | |||||||
| chr8:70683544 | G | A | 4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+2214G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683544 | |||||||
| chr8:70683729 | C | T | 1 | a0001c0001t0004g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.272+2399C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683729 | |||||||
| chr8:70683783 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.272+2453C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683783 | |||||||
| chr8:70683803 | T | G | 2 | a0001c0001t0007g0114 a0001c0001t0018g0196 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.272+2473T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683803 | |||||||
| chr8:70683805 | C | T | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+2475C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683805 | |||||||
| chr8:70683958 | G | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+2628G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683958 | |||||||
| chr8:70683989 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.272+2659T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683989 | |||||||
| chr8:70684021 | T | G | 1 | a0001c0001t0020g0124 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.272+2691T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684021 | |||||||
| chr8:70684142 | A | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+2812A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684142 | |||||||
| chr8:70684255 | G | T | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG02071.hp2 NA18940.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.272+2925G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684255 | |||||||
| chr8:70684298 | C | G | 1 | a0001c0002t0002g0236 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.272+2968C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684298 | |||||||
| chr8:70684302 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.272+2972C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684302 | |||||||
| chr8:70684363 | T | C | 1 | a0001c0001t0004g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.272+3033T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684363 | |||||||
| chr8:70684500 | A | G | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+3170A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684500 | |||||||
| chr8:70684573 | GGTCT | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+3248_272+3251d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70684573 | ||||||
| chr8:70684652 | A | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+3322A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684652 | |||||||
| chr8:70684700 | G | T | 193 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(190): Show |
212 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.272+3370G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684700 | |||||||
| chr8:70684884 | T | C | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+3554T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684884 | |||||||
| chr8:70684894 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.272+3564C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684894 | |||||||
| chr8:70684937 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272+3607C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684937 | |||||||
| chr8:70685037 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+3707C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685037 | |||||||
| chr8:70685038 | G | A | 105 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.272+3708G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685038 | |||||||
| chr8:70685053 | G | T | 105 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.272+3723G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685053 | |||||||
| chr8:70685211 | T | C | 1 | a0001c0002t0002g0253 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.272+3881T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685211 | |||||||
| chr8:70685239 | A | G | 4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+3909A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685239 | |||||||
| chr8:70685262 | G | T | 1 | a0001c0003t0003g0073 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.272+3932G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685262 | |||||||
| chr8:70685276 | G | A | 82 | a0001c0001t0001g0082 a0001c0001t0001g0126 a0001c0002t0002g0004 others(79): Show |
93 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.272+3946G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685276 | |||||||
| chr8:70685346 | G | A | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.272+4016G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685346 | |||||||
| chr8:70685359 | G | C | 59 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(56): Show |
69 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.272+4029G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685359 | |||||||
| chr8:70685408 | A | C | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+4078A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685408 | |||||||
| chr8:70685410 | G | A | 1 | a0001c0006t0007g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.272+4080G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685410 | |||||||
| chr8:70685411 | C | G | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+4081C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685411 | |||||||
| chr8:70685412 | A | G | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+4082A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685412 | |||||||
| chr8:70685422 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.272+4092C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685422 | |||||||
| chr8:70685490 | T | TATA | 62 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(59): Show |
72 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.272+4180_272+4182d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | ||||||
| chr8:70685490 | T | TATAATAA others(2): Show |
12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+4174_272+4182d others(11): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | ||||||
| chr8:70685490 | T | TATAATAA others(8): Show |
1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.272+4168_272+4182d others(17): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | ||||||
| chr8:70685490 | T | TATAATAA others(14): Show |
4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+4162_272+4182d others(23): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | ||||||
| chr8:70685635 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+4305C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685635 | |||||||
| chr8:70685739 | T | A | 4 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0053 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+4409T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685739 | |||||||
| chr8:70685746 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.272+4416A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685746 | |||||||
| chr8:70685749 | G | A | 1 | a0001c0002t0002g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.272+4419G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685749 | |||||||
| chr8:70685752 | G | A | 7 | a0001c0001t0004g0016 a0001c0001t0004g0098 a0001c0001t0004g0099 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.272+4422G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685752 | |||||||
| chr8:70685769 | G | T | 1 | a0001c0002t0002g0235 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.272+4439G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685769 | |||||||
| chr8:70685786 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+4456A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685786 | |||||||
| chr8:70685833 | A | C | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+4503A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685833 | |||||||
| chr8:70685957 | T | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+4627T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685957 | |||||||
| chr8:70686003 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.272+4673A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686003 | |||||||
| chr8:70686006 | T | C | 1 | a0001c0002t0005g0209 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.272+4676T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686006 | |||||||
| chr8:70686071 | G | A | 1 | a0001c0001t0011g0127 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.272+4741G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686071 | |||||||
| chr8:70686240 | CT | C | 159 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(156): Show |
175 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.272+4926delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686240 | ||||||
| chr8:70686240 | CTTTTTTT others(1): Show |
C | 16 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0077 others(13): Show |
18 | HG02738.hp1 HG03942.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.272+4919_272+4926d others(10): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686240 | ||||||
| chr8:70686370 | G | A | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+5040G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686370 | |||||||
| chr8:70686407 | T | G | 1 | a0001c0002t0002g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.272+5077T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686407 | |||||||
| chr8:70686412 | AAT | A | 85 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(82): Show |
105 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.272+5101_272+5102d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686412 | ||||||
| chr8:70686412 | AATAT | A | 79 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(76): Show |
90 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.272+5099_272+5102d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686412 | ||||||
| chr8:70686421 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0171 |
2 | HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.272+5091A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686421 | |||||||
| chr8:70686472 | C | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+5142C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686472 | |||||||
| chr8:70686834 | A | G | 1 | a0001c0001t0004g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.272+5504A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686834 | |||||||
| chr8:70687047 | G | C | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.272+5717G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687047 | |||||||
| chr8:70687088 | T | TC | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+5761dupC | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687088 | ||||||
| chr8:70687179 | C | G | 28 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(25): Show |
32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.272+5849C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687179 | |||||||
| chr8:70687242 | T | C | 1 | a0001c0001t0011g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.272+5912T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687242 | |||||||
| chr8:70687293 | G | T | 113 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(110): Show |
121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.272+5963G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687293 | |||||||
| chr8:70687308 | C | CTTCTCTT others(8): Show |
1 | a0001c0002t0002g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.272+5979_272+5980i others(17): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687308 | ||||||
| chr8:70687310 | C | T | 79 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(76): Show |
90 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.272+5980C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687310 | |||||||
| chr8:70687311 | C | T | 1 | a0001c0002t0002g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.272+5981C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687311 | |||||||
| chr8:70687312 | C | CTCTCTTT others(11): Show |
1 | a0001c0002t0002g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.272+5985_272+5986i others(20): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | C | CTCTT | 54 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0117 others(51): Show |
67 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.272+6026_272+6029d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | C | CTCTTTCT others(1): Show |
66 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0086 others(63): Show |
78 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+6022_272+6029d others(10): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | C | CTCTTTCT others(5): Show |
48 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0083 others(45): Show |
55 | HG00597.hp1 HG00639.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.272+6018_272+6029d others(14): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | C | CTCTTTCT others(9): Show |
24 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
25 | HG00597.hp2 HG01167.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.272+6014_272+6029d others(18): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | C | CTCTTTCT others(13): Show |
5 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0002t0002g0267 others(2): Show |
5 | HG02735.hp1 HG03704.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+6010_272+6029d others(22): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | C | T | 1 | a0001c0002t0002g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.272+5982C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687312 | |||||||
| chr8:70687312 | CTCTT | C | 12 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(9): Show |
12 | HG00140.hp2 HG01081.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.272+6026_272+6029d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | CTCTTTCT others(1): Show |
C | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0004g0015 others(4): Show |
8 | HG01978.hp2 HG02055.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.272+6022_272+6029d others(10): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | CTCTTTCT others(5): Show |
C | 12 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(9): Show |
12 | HG00673.hp1 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.272+6018_272+6029d others(14): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687312 | CTCTTTCT others(9): Show |
C | 24 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0016 others(21): Show |
28 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.272+6014_272+6029d others(18): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | ||||||
| chr8:70687341 | T | TCTTTCTT others(26): Show |
1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.272+6029_272+6030i others(35): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687341 | ||||||
| chr8:70687355 | T | TTTCTTTC others(8): Show |
1 | a0001c0001t0001g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.272+6029_272+6030i others(17): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687355 | ||||||
| chr8:70687358 | C | CTTTCTTT others(3): Show |
1 | a0001c0003t0003g0076 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.272+6029_272+6030i others(12): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687358 | ||||||
| chr8:70687389 | T | C | 229 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(226): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.272+6059T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687389 | |||||||
| chr8:70687395 | T | TTC | 113 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(110): Show |
121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.272+6080_272+6081d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687395 | ||||||
| chr8:70687552 | T | A | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+6222T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687552 | |||||||
| chr8:70687817 | T | G | 9 | a0001c0001t0004g0012 a0001c0001t0004g0016 a0001c0001t0004g0045 others(6): Show |
11 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.272+6487T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687817 | |||||||
| chr8:70687866 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+6536C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687866 | |||||||
| chr8:70688099 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.272+6769C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688099 | |||||||
| chr8:70688239 | G | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+6909G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688239 | |||||||
| chr8:70688336 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.272+7006C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688336 | |||||||
| chr8:70688375 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+7045C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688375 | |||||||
| chr8:70688437 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(29): Show |
36 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.272+7107G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688437 | |||||||
| chr8:70688618 | A | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.272+7288A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688618 | |||||||
| chr8:70688635 | C | G | 1 | a0002c0004t0009g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.272+7305C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688635 | |||||||
| chr8:70688707 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+7377T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688707 | |||||||
| chr8:70688715 | C | CT | 82 | a0001c0001t0001g0163 a0001c0001t0001g0197 a0001c0001t0004g0037 others(79): Show |
93 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.272+7399dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70688715 | ||||||
| chr8:70688761 | C | G | 64 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(61): Show |
74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.272+7431C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688761 | |||||||
| chr8:70688767 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.272+7437T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688767 | |||||||
| chr8:70688916 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.272+7586C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688916 | |||||||
| chr8:70689017 | C | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+7687C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689017 | |||||||
| chr8:70689044 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.272+7714A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689044 | |||||||
| chr8:70689047 | C | T | 1 | a0001c0002t0002g0026 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.272+7717C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689047 | |||||||
| chr8:70689306 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+7976T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689306 | |||||||
| chr8:70689319 | A | T | 17 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0028 others(14): Show |
23 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.272+7989A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689319 | |||||||
| chr8:70689341 | A | G | 1 | a0001c0006t0007g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.272+8011A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689341 | |||||||
| chr8:70689443 | AAT | A | 76 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(73): Show |
87 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.272+8128_272+8129d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70689443 | ||||||
| chr8:70689486 | T | A | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+8156T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689486 | |||||||
| chr8:70689499 | TTA | T | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+8179_272+8180d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70689499 | ||||||
| chr8:70689513 | A | G | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.272+8183A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689513 | |||||||
| chr8:70689652 | T | C | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+8322T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689652 | |||||||
| chr8:70689681 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.272+8351C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689681 | |||||||
| chr8:70689708 | A | G | 4 | a0001c0002t0005g0209 a0001c0002t0005g0212 a0001c0002t0005g0213 others(1): Show |
4 | HG01074.hp2 HG02004.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+8378A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689708 | |||||||
| chr8:70689774 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+8444A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689774 | |||||||
| chr8:70690109 | A | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+8779A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690109 | |||||||
| chr8:70690159 | A | C | 1 | a0001c0001t0017g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.272+8829A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690159 | |||||||
| chr8:70690500 | G | GT | 62 | a0001c0001t0001g0118 a0001c0001t0001g0161 a0001c0001t0001g0163 others(59): Show |
70 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.272+9185dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70690500 | ||||||
| chr8:70690500 | G | GTT | 14 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0244 others(11): Show |
15 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.272+9184_272+9185d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70690500 | ||||||
| chr8:70690517 | T | G | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+9187T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690517 | |||||||
| chr8:70690602 | G | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+9272G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690602 | |||||||
| chr8:70690638 | C | T | 1 | a0001c0002t0002g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.272+9308C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690638 | |||||||
| chr8:70690679 | A | G | 1 | a0001c0001t0010g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.272+9349A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690679 | |||||||
| chr8:70690715 | T | A | 4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+9385T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690715 | |||||||
| chr8:70690760 | G | T | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.272+9430G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690760 | |||||||
| chr8:70690844 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.272+9514G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690844 | |||||||
| chr8:70690879 | A | G | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+9549A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690879 | |||||||
| chr8:70690952 | G | A | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.272+9622G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690952 | |||||||
| chr8:70691296 | A | T | 1 | a0001c0001t0004g0036 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.272+9966A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691296 | |||||||
| chr8:70691422 | C | T | 1 | a0001c0002t0002g0026 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.272+10092C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691422 | |||||||
| chr8:70691425 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.272+10095A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691425 | |||||||
| chr8:70691533 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.272+10203T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691533 | |||||||
| chr8:70691646 | C | G | 2 | a0001c0002t0002g0266 a0001c0002t0002g0267 |
2 | NA19066.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.272+10316C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691646 | |||||||
| chr8:70691710 | G | A | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+10380G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691710 | |||||||
| chr8:70691719 | G | A | 2 | a0001c0001t0016g0078 a0001c0001t0017g0031 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.272+10389G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691719 | |||||||
| chr8:70691728 | A | G | 1 | a0001c0001t0019g0147 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.272+10398A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691728 | |||||||
| chr8:70691749 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+10419A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691749 | |||||||
| chr8:70691903 | T | G | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+10573T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691903 | |||||||
| chr8:70691929 | A | T | 1 | a0001c0001t0004g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.272+10599A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691929 | |||||||
| chr8:70692028 | A | ATTC | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+10701_272+1070 others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70692028 | ||||||
| chr8:70692061 | T | C | 2 | a0001c0002t0008g0249 a0001c0002t0008g0250 |
2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.272+10731T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692061 | |||||||
| chr8:70692179 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+10849C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692179 | |||||||
| chr8:70692406 | G | GT | 69 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(66): Show |
79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+11085dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70692406 | ||||||
| chr8:70692470 | A | G | 1 | a0003c0007t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.272+11140A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692470 | |||||||
| chr8:70692577 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.272+11247T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692577 | |||||||
| chr8:70692588 | AT | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+11265delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70692588 | ||||||
| chr8:70692682 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+11352G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692682 | |||||||
| chr8:70692768 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.272+11438C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692768 | |||||||
| chr8:70692918 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0150 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.272+11588T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692918 | |||||||
| chr8:70693420 | T | C | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.272+12090T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70693420 | |||||||
| chr8:70693692 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+12362C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70693692 | |||||||
| chr8:70693811 | T | C | 1 | a0001c0002t0023g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.272+12481T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70693811 | |||||||
| chr8:70693909 | A | AGTT | 6 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.272+12581_272+1258 others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70693909 | ||||||
| chr8:70694000 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+12670G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694000 | |||||||
| chr8:70694107 | TC | T | 113 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(110): Show |
121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.272+12778delC | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694107 | |||||||
| chr8:70694412 | G | T | 1 | a0001c0003t0003g0073 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.273-12521G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694412 | |||||||
| chr8:70694430 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.273-12503G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694430 | |||||||
| chr8:70694545 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0134 |
2 | NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.273-12388C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694545 | |||||||
| chr8:70694622 | A | G | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.273-12311A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694622 | |||||||
| chr8:70694651 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-12282C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694651 | |||||||
| chr8:70694711 | A | G | 1 | a0001c0002t0002g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.273-12222A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694711 | |||||||
| chr8:70694848 | T | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-12085T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694848 | |||||||
| chr8:70694927 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0154 |
2 | HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.273-12006A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694927 | |||||||
| chr8:70695002 | G | T | 28 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(25): Show |
32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.273-11931G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695002 | |||||||
| chr8:70695128 | CT | C | 111 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(108): Show |
125 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.273-11788delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695128 | ||||||
| chr8:70695128 | CTT | C | 7 | a0001c0001t0001g0206 a0001c0002t0002g0233 a0001c0002t0002g0260 others(4): Show |
7 | HG01167.hp2 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.273-11789_273-1178 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695128 | ||||||
| chr8:70695128 | CTTTTTTT | C | 24 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(21): Show |
25 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.273-11794_273-1178 others(11): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695128 | ||||||
| chr8:70695162 | T | A | 1 | a0001c0003t0003g0073 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.273-11771T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695162 | |||||||
| chr8:70695163 | A | T | 13 | a0001c0001t0004g0044 a0001c0001t0004g0106 a0001c0002t0005g0023 others(10): Show |
14 | HG00642.hp1 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.273-11770A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695163 | |||||||
| chr8:70695169 | A | T | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-11764A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695169 | |||||||
| chr8:70695169 | AT | A | 5 | a0001c0002t0002g0255 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-11755delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695169 | ||||||
| chr8:70695170 | T | A | 109 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(106): Show |
124 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.273-11763T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695170 | |||||||
| chr8:70695174 | T | A | 2 | a0001c0001t0001g0184 a0002c0004t0002g0238 |
2 | HG01074.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273-11759T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695174 | |||||||
| chr8:70695259 | A | G | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.273-11674A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695259 | |||||||
| chr8:70695277 | T | C | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-11656T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695277 | |||||||
| chr8:70695327 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-11606C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695327 | |||||||
| chr8:70695329 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-11604C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695329 | |||||||
| chr8:70695332 | G | C | 229 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(226): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.273-11601G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695332 | |||||||
| chr8:70695354 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-11579A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695354 | |||||||
| chr8:70695391 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-11542C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695391 | |||||||
| chr8:70695432 | G | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-11501G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695432 | |||||||
| chr8:70695580 | T | A | 1 | a0001c0001t0004g0042 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.273-11353T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695580 | |||||||
| chr8:70695628 | C | T | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-11305C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695628 | |||||||
| chr8:70695639 | C | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.273-11294C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695639 | |||||||
| chr8:70695676 | C | A | 1 | a0001c0002t0005g0213 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.273-11257C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695676 | |||||||
| chr8:70695691 | T | C | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273-11242T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695691 | |||||||
| chr8:70695747 | T | C | 81 | a0001c0001t0001g0125 a0001c0002t0002g0004 a0001c0002t0002g0010 others(78): Show |
92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-11186T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695747 | |||||||
| chr8:70695768 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-11165G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695768 | |||||||
| chr8:70695769 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-11164G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695769 | |||||||
| chr8:70695784 | A | G | 79 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(76): Show |
90 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.273-11149A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695784 | |||||||
| chr8:70695788 | C | A | 1 | a0001c0001t0012g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.273-11145C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695788 | |||||||
| chr8:70695852 | C | T | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.273-11081C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695852 | |||||||
| chr8:70695901 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-11032T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695901 | |||||||
| chr8:70695985 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.273-10948A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695985 | |||||||
| chr8:70695993 | T | C | 4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-10940T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695993 | |||||||
| chr8:70696042 | T | C | 1 | a0001c0001t0014g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.273-10891T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696042 | |||||||
| chr8:70696088 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.273-10845T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696088 | |||||||
| chr8:70696093 | G | C | 5 | a0001c0001t0001g0086 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-10840G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696093 | |||||||
| chr8:70696109 | A | T | 1 | a0001c0001t0003g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.273-10824A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696109 | |||||||
| chr8:70696215 | C | T | 33 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(30): Show |
37 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.273-10718C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696215 | |||||||
| chr8:70696317 | C | T | 1 | a0001c0002t0023g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.273-10616C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696317 | |||||||
| chr8:70696322 | C | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10611C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696322 | |||||||
| chr8:70696323 | A | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10610A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696323 | |||||||
| chr8:70696361 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-10572A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696361 | |||||||
| chr8:70696436 | G | C | 1 | a0001c0002t0002g0277 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.273-10497G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696436 | |||||||
| chr8:70696497 | A | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.273-10436A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696497 | |||||||
| chr8:70696519 | T | C | 4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-10414T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696519 | |||||||
| chr8:70696568 | C | G | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-10365C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696568 | |||||||
| chr8:70696599 | T | C | 1 | a0001c0002t0002g0247 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273-10334T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696599 | |||||||
| chr8:70696655 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.273-10278C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696655 | |||||||
| chr8:70696662 | G | A | 229 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(226): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.273-10271G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696662 | |||||||
| chr8:70696663 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10270C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696663 | |||||||
| chr8:70696673 | C | T | 276 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(273): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.273-10260C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696673 | |||||||
| chr8:70696677 | T | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-10256T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696677 | |||||||
| chr8:70696699 | GT | G | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-10228delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70696699 | ||||||
| chr8:70696832 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10101G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696832 | |||||||
| chr8:70696852 | A | C | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.273-10081A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696852 | |||||||
| chr8:70696899 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-10034A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696899 | |||||||
| chr8:70696936 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-9997T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696936 | |||||||
| chr8:70697158 | A | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-9775A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697158 | |||||||
| chr8:70697159 | G | A | 69 | a0001c0001t0001g0183 a0001c0002t0002g0004 a0001c0002t0002g0010 others(66): Show |
79 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-9774G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697159 | |||||||
| chr8:70697250 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.273-9683C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697250 | |||||||
| chr8:70697323 | T | C | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-9610T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697323 | |||||||
| chr8:70697352 | T | C | 1 | a0001c0002t0002g0268 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.273-9581T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697352 | |||||||
| chr8:70697396 | G | A | 1 | a0001c0001t0004g0098 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273-9537G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697396 | |||||||
| chr8:70697418 | C | G | 1 | a0001c0001t0003g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.273-9515C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697418 | |||||||
| chr8:70697556 | C | G | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-9377C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697556 | |||||||
| chr8:70697667 | C | A | 37 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(34): Show |
41 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.273-9266C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697667 | |||||||
| chr8:70697774 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273-9159T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697774 | |||||||
| chr8:70697792 | C | T | 67 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(64): Show |
77 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.273-9141C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697792 | |||||||
| chr8:70697799 | G | GA | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-9132dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70697799 | ||||||
| chr8:70697802 | T | G | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-9131T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697802 | |||||||
| chr8:70697830 | G | A | 2 | a0001c0001t0004g0081 a0005c0009t0004g0079 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.273-9103G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697830 | |||||||
| chr8:70697861 | C | A | 5 | a0001c0001t0004g0039 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-9072C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697861 | |||||||
| chr8:70697885 | A | T | 1 | a0001c0001t0016g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273-9048A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697885 | |||||||
| chr8:70697982 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.273-8951G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697982 | |||||||
| chr8:70698020 | C | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-8913C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698020 | |||||||
| chr8:70698020 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.273-8913C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698020 | |||||||
| chr8:70698052 | T | G | 2 | a0001c0001t0001g0170 a0002c0004t0002g0238 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273-8881T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698052 | |||||||
| chr8:70698132 | C | T | 4 | a0001c0001t0004g0013 a0001c0001t0004g0034 a0001c0001t0004g0042 others(1): Show |
5 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-8801C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698132 | |||||||
| chr8:70698194 | C | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-8739C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698194 | |||||||
| chr8:70698204 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-8729A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698204 | |||||||
| chr8:70698365 | A | C | 1 | a0001c0001t0003g0028 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.273-8568A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698365 | |||||||
| chr8:70698542 | C | T | 2 | a0001c0002t0002g0230 a0001c0002t0002g0237 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.273-8391C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698542 | |||||||
| chr8:70698545 | A | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-8388A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698545 | |||||||
| chr8:70698550 | C | G | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273-8383C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698550 | |||||||
| chr8:70698574 | T | C | 28 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(25): Show |
32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.273-8359T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698574 | |||||||
| chr8:70698663 | T | C | 6 | a0001c0002t0005g0023 a0001c0002t0005g0209 a0001c0002t0005g0210 others(3): Show |
7 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.273-8270T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698663 | |||||||
| chr8:70698702 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-8231C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698702 | |||||||
| chr8:70698740 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0103 |
3 | HG01884.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.273-8193C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698740 | |||||||
| chr8:70698841 | G | A | 115 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(112): Show |
130 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(127): Show |
intron_variant | MODIFIER | c.273-8092G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698841 | |||||||
| chr8:70698924 | C | T | 6 | a0001c0002t0005g0023 a0001c0002t0005g0209 a0001c0002t0005g0210 others(3): Show |
7 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.273-8009C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698924 | |||||||
| chr8:70698998 | G | T | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-7935G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698998 | |||||||
| chr8:70699086 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-7847G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699086 | |||||||
| chr8:70699182 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-7751G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699182 | |||||||
| chr8:70699210 | T | A | 3 | a0001c0002t0008g0249 a0001c0002t0008g0250 a0001c0002t0008g0251 |
3 | HG02965.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.273-7723T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699210 | |||||||
| chr8:70699453 | T | G | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.273-7480T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699453 | |||||||
| chr8:70699465 | T | A | 279 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(276): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.273-7468T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699465 | |||||||
| chr8:70699468 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-7465C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699468 | |||||||
| chr8:70699561 | C | T | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.273-7372C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699561 | |||||||
| chr8:70699621 | A | T | 1 | a0001c0002t0002g0276 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.273-7312A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699621 | |||||||
| chr8:70699655 | C | T | 14 | a0001c0001t0004g0106 a0001c0002t0002g0263 a0001c0002t0005g0023 others(11): Show |
15 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.273-7278C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699655 | |||||||
| chr8:70699678 | G | A | 1 | a0001c0002t0002g0223 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.273-7255G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699678 | |||||||
| chr8:70699792 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-7141C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699792 | |||||||
| chr8:70699802 | T | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-7131T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699802 | |||||||
| chr8:70699822 | A | G | 1 | a0001c0002t0002g0276 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.273-7111A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699822 | |||||||
| chr8:70699942 | A | G | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.273-6991A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699942 | |||||||
| chr8:70700049 | C | A | 1 | a0001c0001t0003g0057 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.273-6884C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700049 | |||||||
| chr8:70700069 | A | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-6864A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700069 | |||||||
| chr8:70700166 | C | A | 4 | a0001c0001t0004g0013 a0001c0001t0004g0034 a0001c0001t0004g0042 others(1): Show |
5 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-6767C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700166 | |||||||
| chr8:70700185 | C | G | 4 | a0001c0001t0004g0015 a0001c0001t0004g0095 a0001c0001t0004g0096 others(1): Show |
5 | HG02055.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-6748C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700185 | |||||||
| chr8:70700236 | C | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-6697C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700236 | |||||||
| chr8:70700300 | C | T | 1 | a0001c0001t0004g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273-6633C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700300 | |||||||
| chr8:70700300 | CCT | C | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-6630_273-6629d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70700300 | ||||||
| chr8:70700478 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-6455C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700478 | |||||||
| chr8:70700540 | G | A | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.273-6393G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700540 | |||||||
| chr8:70700637 | GGGACCCA others(5): Show |
G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0075 |
3 | NA18944.hp1 NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.273-6292_273-6281d others(14): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70700637 | ||||||
| chr8:70700684 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-6249C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700684 | |||||||
| chr8:70700781 | T | C | 1 | a0001c0002t0002g0236 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273-6152T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700781 | |||||||
| chr8:70700844 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-6089T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700844 | |||||||
| chr8:70700854 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-6079A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700854 | |||||||
| chr8:70700866 | T | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-6067T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700866 | |||||||
| chr8:70700992 | G | T | 1 | a0001c0001t0017g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.273-5941G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700992 | |||||||
| chr8:70701070 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.273-5863T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701070 | |||||||
| chr8:70701157 | G | A | 1 | a0001c0001t0003g0047 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.273-5776G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701157 | |||||||
| chr8:70701201 | C | T | 1 | a0001c0001t0004g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.273-5732C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701201 | |||||||
| chr8:70701237 | G | A | 83 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0162 others(80): Show |
94 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.273-5696G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701237 | |||||||
| chr8:70701276 | C | T | 1 | a0001c0002t0002g0236 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273-5657C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701276 | |||||||
| chr8:70701277 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.273-5656G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701277 | |||||||
| chr8:70701480 | A | G | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG02071.hp2 NA18940.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.273-5453A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701480 | |||||||
| chr8:70701574 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.273-5359G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701574 | |||||||
| chr8:70701628 | T | G | 1 | a0001c0002t0002g0257 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.273-5305T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701628 | |||||||
| chr8:70701795 | G | A | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-5138G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701795 | |||||||
| chr8:70701808 | A | G | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.273-5125A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701808 | |||||||
| chr8:70702012 | C | T | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.273-4921C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702012 | |||||||
| chr8:70702386 | G | T | 1 | a0001c0002t0002g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.273-4547G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702386 | |||||||
| chr8:70702543 | C | T | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0016 others(27): Show |
33 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-4390C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702543 | |||||||
| chr8:70702546 | A | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-4387A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702546 | |||||||
| chr8:70702896 | A | G | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-4037A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702896 | |||||||
| chr8:70703136 | A | G | 1 | a0001c0002t0005g0023 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.273-3797A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703136 | |||||||
| chr8:70703167 | GT | G | 113 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0193 others(110): Show |
128 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.273-3756delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70703167 | ||||||
| chr8:70703212 | A | T | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-3721A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703212 | |||||||
| chr8:70703318 | T | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-3615T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703318 | |||||||
| chr8:70703341 | G | A | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273-3592G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703341 | |||||||
| chr8:70703365 | C | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-3568C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703365 | |||||||
| chr8:70703481 | G | A | 106 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(103): Show |
114 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.273-3452G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703481 | |||||||
| chr8:70703727 | G | T | 88 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(85): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.273-3206G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703727 | |||||||
| chr8:70703819 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.273-3114T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703819 | |||||||
| chr8:70703876 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0140 others(3): Show |
6 | HG00673.hp2 NA18971.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.273-3057T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703876 | |||||||
| chr8:70704089 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.273-2844G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704089 | |||||||
| chr8:70704107 | G | A | 1 | a0001c0003t0003g0065 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.273-2826G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704107 | |||||||
| chr8:70704117 | G | A | 1 | a0001c0001t0004g0098 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273-2816G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704117 | |||||||
| chr8:70704303 | C | G | 4 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-2630C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704303 | |||||||
| chr8:70704420 | G | C | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.273-2513G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704420 | |||||||
| chr8:70704448 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.273-2485T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704448 | |||||||
| chr8:70704664 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.273-2269G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704664 | |||||||
| chr8:70704694 | A | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-2239A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704694 | |||||||
| chr8:70704747 | A | C | 168 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(165): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.273-2186A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704747 | |||||||
| chr8:70704759 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0082 a0001c0001t0001g0126 others(5): Show |
9 | HG01175.hp1 HG02056.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-2174A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704759 | |||||||
| chr8:70704810 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-2123G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704810 | |||||||
| chr8:70704873 | C | G | 1 | a0001c0001t0015g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.273-2060C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704873 | |||||||
| chr8:70704961 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.273-1972A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704961 | |||||||
| chr8:70705181 | A | G | 1 | a0001c0002t0002g0253 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.273-1752A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705181 | |||||||
| chr8:70705203 | ACTTCAGT others(17): Show |
A | 5 | a0001c0001t0004g0013 a0001c0001t0004g0032 a0001c0001t0004g0034 others(2): Show |
6 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.273-1727_273-1704d others(26): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70705203 | ||||||
| chr8:70705447 | A | G | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273-1486A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705447 | |||||||
| chr8:70705480 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-1453A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705480 | |||||||
| chr8:70705613 | A | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-1320A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705613 | |||||||
| chr8:70705685 | G | T | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.273-1248G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705685 | |||||||
| chr8:70705859 | C | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-1074C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705859 | |||||||
| chr8:70706058 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-875A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706058 | |||||||
| chr8:70706149 | A | G | 1 | a0001c0001t0004g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273-784A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706149 | |||||||
| chr8:70706223 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0154 |
2 | HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.273-710C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706223 | |||||||
| chr8:70706239 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-694C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706239 | |||||||
| chr8:70706425 | C | G | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.273-508C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706425 | |||||||
| chr8:70706532 | T | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-401T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706532 | |||||||
| chr8:70706635 | C | A | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.273-298C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706635 | |||||||
| chr8:70706739 | A | G | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273-194A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706739 | |||||||
| chr8:70706859 | AATT | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-68_273-66delTA others(1): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70706859 | ||||||
| chr8:70707550 | T | C | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+397T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70707550 | |||||||
| chr8:70707607 | GGTT | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+458_493+460del others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70707607 | ||||||
| chr8:70707723 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0188 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.493+570G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70707723 | |||||||
| chr8:70707838 | C | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+685C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70707838 | |||||||
| chr8:70708023 | T | C | 1 | a0001c0001t0004g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.493+870T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708023 | |||||||
| chr8:70708052 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+899C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708052 | |||||||
| chr8:70708287 | A | G | 1 | a0001c0002t0005g0023 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.493+1134A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708287 | |||||||
| chr8:70708363 | A | G | 1 | a0001c0002t0008g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.493+1210A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708363 | |||||||
| chr8:70708376 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | NA19002.hp1 NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.493+1223T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708376 | |||||||
| chr8:70708423 | C | T | 8 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0221 others(5): Show |
10 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.493+1270C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708423 | |||||||
| chr8:70708510 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.493+1357C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708510 | |||||||
| chr8:70708546 | A | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1393A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708546 | |||||||
| chr8:70708561 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.493+1408C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708561 | |||||||
| chr8:70708725 | A | C | 1 | a0001c0001t0012g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493+1572A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708725 | |||||||
| chr8:70708838 | C | T | 1 | a0001c0002t0002g0252 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.493+1685C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708838 | |||||||
| chr8:70708955 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+1802G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708955 | |||||||
| chr8:70708966 | A | G | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.493+1813A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708966 | |||||||
| chr8:70709033 | G | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+1880G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709033 | |||||||
| chr8:70709058 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.493+1905A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709058 | |||||||
| chr8:70709481 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2328G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709481 | |||||||
| chr8:70709617 | A | T | 1 | a0001c0001t0003g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.493+2464A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709617 | |||||||
| chr8:70709972 | C | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2819C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709972 | |||||||
| chr8:70709974 | A | G | 4 | a0001c0001t0004g0013 a0001c0001t0004g0034 a0001c0001t0004g0042 others(1): Show |
5 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+2821A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709974 | |||||||
| chr8:70709991 | T | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2838T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709991 | |||||||
| chr8:70710100 | C | G | 50 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(47): Show |
64 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.493+2947C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710100 | |||||||
| chr8:70710138 | A | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+2985A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710138 | |||||||
| chr8:70710156 | T | C | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.493+3003T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710156 | |||||||
| chr8:70710169 | C | T | 28 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(25): Show |
32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.493+3016C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710169 | |||||||
| chr8:70710273 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+3120C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710273 | |||||||
| chr8:70710293 | A | G | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(49): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+3140A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710293 | |||||||
| chr8:70710438 | T | C | 168 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(165): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.493+3285T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710438 | |||||||
| chr8:70710617 | C | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+3464C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710617 | |||||||
| chr8:70710618 | G | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+3465G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710618 | |||||||
| chr8:70710695 | C | T | 2 | a0001c0001t0016g0078 a0001c0001t0017g0031 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+3542C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710695 | |||||||
| chr8:70710699 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.493+3546A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710699 | |||||||
| chr8:70710702 | TCAAACAA | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+3553_493+3559d others(9): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70710702 | ||||||
| chr8:70710704 | AAAC | A | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+3569_493+3571d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70710704 | ||||||
| chr8:70710716 | C | G | 2 | a0001c0001t0016g0078 a0001c0001t0017g0031 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+3563C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710716 | |||||||
| chr8:70710761 | A | C | 2 | a0001c0001t0016g0078 a0001c0001t0017g0031 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+3608A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710761 | |||||||
| chr8:70710795 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493+3642A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710795 | |||||||
| chr8:70710820 | G | T | 1 | a0001c0001t0017g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+3667G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710820 | |||||||
| chr8:70710910 | A | G | 3 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 |
3 | HG02630.hp1 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.493+3757A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710910 | |||||||
| chr8:70710950 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.493+3797C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710950 | |||||||
| chr8:70710951 | G | A | 1 | a0001c0002t0002g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.493+3798G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710951 | |||||||
| chr8:70711078 | C | G | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+3925C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711078 | |||||||
| chr8:70711130 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493+3977T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711130 | |||||||
| chr8:70711152 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+3999G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711152 | |||||||
| chr8:70711371 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.493+4218A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711371 | |||||||
| chr8:70711532 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.493+4379C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711532 | |||||||
| chr8:70711585 | T | TAAACACA others(197): Show |
7 | a0001c0001t0004g0015 a0001c0001t0004g0081 a0001c0001t0004g0095 others(4): Show |
8 | HG01167.hp1 HG02055.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.493+4640_493+4843d others(206): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711585 | ||||||
| chr8:70711585 | TAAACACA others(197): Show |
T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+4640_493+4843d others(2): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711585 | ||||||
| chr8:70711605 | A | ATAGACAT others(197): Show |
1 | a0001c0001t0017g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+4655_493+4656i others(206): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711605 | ||||||
| chr8:70711732 | A | AATTTACC others(197): Show |
1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+4782_493+4783i others(206): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711732 | ||||||
| chr8:70711809 | A | G | 2 | a0001c0001t0016g0078 a0001c0001t0017g0031 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+4656A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711809 | |||||||
| chr8:70711924 | C | T | 51 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(48): Show |
59 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.493+4771C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711924 | |||||||
| chr8:70712397 | A | G | 50 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(47): Show |
64 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.493+5244A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712397 | |||||||
| chr8:70712705 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.493+5552A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712705 | |||||||
| chr8:70712765 | A | G | 1 | a0001c0001t0016g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.493+5612A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712765 | |||||||
| chr8:70712986 | C | T | 1 | a0001c0001t0017g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+5833C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712986 | |||||||
| chr8:70713001 | A | G | 1 | a0001c0002t0002g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.493+5848A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713001 | |||||||
| chr8:70713163 | A | C | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.493+6010A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713163 | |||||||
| chr8:70713268 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+6115G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713268 | |||||||
| chr8:70713301 | G | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+6148G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713301 | |||||||
| chr8:70713353 | T | A | 1 | a0001c0002t0002g0276 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.493+6200T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713353 | |||||||
| chr8:70713453 | G | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+6300G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713453 | |||||||
| chr8:70713669 | TAAG | T | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.493+6525_493+6527d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70713669 | ||||||
| chr8:70713712 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.493+6559C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713712 | |||||||
| chr8:70713863 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+6710A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713863 | |||||||
| chr8:70714040 | T | C | 176 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(173): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.493+6887T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714040 | |||||||
| chr8:70714122 | C | G | 1 | a0001c0003t0003g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.493+6969C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714122 | |||||||
| chr8:70714129 | T | C | 269 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(266): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.493+6976T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714129 | |||||||
| chr8:70714282 | A | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0140 others(3): Show |
6 | HG00673.hp2 NA18971.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+7129A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714282 | |||||||
| chr8:70714328 | T | C | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+7175T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714328 | |||||||
| chr8:70714428 | A | G | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+7275A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714428 | |||||||
| chr8:70714432 | T | C | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.493+7279T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714432 | |||||||
| chr8:70714449 | CTGAT | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+7299_493+7302d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70714449 | ||||||
| chr8:70714455 | G | A | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+7302G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714455 | |||||||
| chr8:70714475 | T | C | 1 | a0001c0001t0017g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+7322T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714475 | |||||||
| chr8:70714488 | T | C | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+7335T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714488 | |||||||
| chr8:70714537 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+7384G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714537 | |||||||
| chr8:70714681 | A | T | 1 | a0001c0002t0005g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.493+7528A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714681 | |||||||
| chr8:70714717 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.493+7564G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714717 | |||||||
| chr8:70714718 | C | T | 13 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(10): Show |
14 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.493+7565C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714718 | |||||||
| chr8:70714771 | A | T | 1 | a0001c0001t0003g0072 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.493+7618A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714771 | |||||||
| chr8:70715009 | G | C | 1 | a0001c0002t0002g0245 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493+7856G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715009 | |||||||
| chr8:70715209 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.493+8056A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715209 | |||||||
| chr8:70715256 | T | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+8103T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715256 | |||||||
| chr8:70715270 | A | G | 7 | a0001c0001t0004g0016 a0001c0001t0004g0098 a0001c0001t0004g0099 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+8117A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715270 | |||||||
| chr8:70715372 | A | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8219A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715372 | |||||||
| chr8:70715420 | A | G | 1 | a0001c0001t0014g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.493+8267A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715420 | |||||||
| chr8:70715487 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8334C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715487 | |||||||
| chr8:70715510 | G | T | 1 | a0001c0001t0007g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.493+8357G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715510 | |||||||
| chr8:70715718 | A | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+8565A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715718 | |||||||
| chr8:70715744 | A | C | 4 | a0001c0001t0011g0116 a0001c0001t0011g0127 a0001c0001t0011g0201 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+8591A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715744 | |||||||
| chr8:70715777 | A | C | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+8624A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715777 | |||||||
| chr8:70715795 | C | G | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(49): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+8642C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715795 | |||||||
| chr8:70715833 | G | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+8680G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715833 | |||||||
| chr8:70715840 | A | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+8687A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715840 | |||||||
| chr8:70715851 | A | C | 176 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(173): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.493+8698A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715851 | |||||||
| chr8:70715861 | G | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8708G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715861 | |||||||
| chr8:70715976 | A | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8823A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715976 | |||||||
| chr8:70716064 | A | G | 1 | a0002c0004t0009g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.493+8911A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716064 | |||||||
| chr8:70716228 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+9075G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716228 | |||||||
| chr8:70716335 | G | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+9182G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716335 | |||||||
| chr8:70716433 | TG | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+9286delG | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70716433 | ||||||
| chr8:70716439 | G | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+9286G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716439 | |||||||
| chr8:70716445 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+9292G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716445 | |||||||
| chr8:70716483 | T | G | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+9330T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716483 | |||||||
| chr8:70716518 | G | A | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.493+9365G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716518 | |||||||
| chr8:70716708 | C | A | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+9555C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716708 | |||||||
| chr8:70716908 | T | G | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+9755T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716908 | |||||||
| chr8:70716929 | T | TA | 9 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0198 others(6): Show |
10 | HG02165.hp1 NA18612.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.493+9777dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70716929 | ||||||
| chr8:70717227 | C | T | 1 | a0001c0001t0004g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+10074C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717227 | |||||||
| chr8:70717241 | CTG | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+10090_493+1009 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70717241 | ||||||
| chr8:70717257 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493+10104C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717257 | |||||||
| chr8:70717474 | T | A | 4 | a0001c0001t0004g0035 a0001c0001t0004g0040 a0001c0001t0004g0041 others(1): Show |
4 | HG01192.hp2 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+10321T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717474 | |||||||
| chr8:70717575 | G | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+10422G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717575 | |||||||
| chr8:70717720 | C | G | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.493+10567C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717720 | |||||||
| chr8:70717785 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.493+10632C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717785 | |||||||
| chr8:70718000 | C | T | 1 | a0001c0002t0002g0253 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.493+10847C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718000 | |||||||
| chr8:70718110 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.493+10957A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718110 | |||||||
| chr8:70718119 | A | G | 1 | a0001c0001t0004g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+10966A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718119 | |||||||
| chr8:70718164 | A | G | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(49): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+11011A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718164 | |||||||
| chr8:70718192 | A | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+11039A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718192 | |||||||
| chr8:70718213 | A | G | 1 | a0001c0002t0002g0025 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.493+11060A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718213 | |||||||
| chr8:70718301 | ATTAT | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+11159_493+1116 others(8): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70718301 | ||||||
| chr8:70718319 | TTTTAC | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+11171_493+1117 others(9): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70718319 | ||||||
| chr8:70718552 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(42): Show |
59 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.493+11399A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718552 | |||||||
| chr8:70718669 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.493+11516G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718669 | |||||||
| chr8:70718818 | C | A | 1 | a0001c0002t0002g0263 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493+11665C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718818 | |||||||
| chr8:70718855 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.493+11702A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718855 | |||||||
| chr8:70718873 | T | C | 52 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(49): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+11720T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718873 | |||||||
| chr8:70718896 | C | T | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+11743C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718896 | |||||||
| chr8:70718938 | G | T | 1 | a0001c0001t0021g0084 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.493+11785G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718938 | |||||||
| chr8:70719026 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+11873G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719026 | |||||||
| chr8:70719160 | T | G | 1 | a0001c0002t0002g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.493+12007T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719160 | |||||||
| chr8:70719246 | C | T | 1 | a0001c0001t0015g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.493+12093C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719246 | |||||||
| chr8:70719264 | C | T | 1 | a0001c0002t0008g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.493+12111C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719264 | |||||||
| chr8:70719290 | C | T | 1 | a0001c0001t0014g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.493+12137C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719290 | |||||||
| chr8:70719303 | G | T | 1 | a0001c0002t0002g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.493+12150G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719303 | |||||||
| chr8:70719529 | C | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.493+12376C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719529 | |||||||
| chr8:70720091 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+12938C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720091 | |||||||
| chr8:70720116 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.493+12963G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720116 | |||||||
| chr8:70720210 | G | C | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+13057G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720210 | |||||||
| chr8:70720282 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.493+13129C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720282 | |||||||
| chr8:70720283 | C | G | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+13130C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720283 | |||||||
| chr8:70720283 | C | T | 1 | a0001c0002t0002g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.493+13130C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720283 | |||||||
| chr8:70720509 | G | A | 1 | a0001c0001t0019g0147 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.494-13287G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720509 | |||||||
| chr8:70720658 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-13138C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720658 | |||||||
| chr8:70720741 | G | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02615.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-13055G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720741 | |||||||
| chr8:70720989 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.494-12807G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720989 | |||||||
| chr8:70721022 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-12774G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721022 | |||||||
| chr8:70721044 | C | G | 28 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(25): Show |
32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.494-12752C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721044 | |||||||
| chr8:70721156 | T | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-12640T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721156 | |||||||
| chr8:70721219 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.494-12577G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721219 | |||||||
| chr8:70721299 | C | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-12497C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721299 | |||||||
| chr8:70721313 | C | G | 2 | a0001c0002t0002g0262 a0001c0002t0002g0265 |
2 | NA18949.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.494-12483C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721313 | |||||||
| chr8:70721543 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-12253T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721543 | |||||||
| chr8:70721544 | T | C | 4 | a0001c0002t0002g0232 a0001c0002t0002g0247 a0001c0002t0002g0248 others(1): Show |
4 | HG00733.hp2 HG01255.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-12252T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721544 | |||||||
| chr8:70721591 | T | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-12205T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721591 | |||||||
| chr8:70721607 | C | T | 1 | a0001c0006t0007g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.494-12189C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721607 | |||||||
| chr8:70721610 | T | C | 2 | a0001c0002t0002g0025 a0001c0002t0002g0227 |
3 | HG02922.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.494-12186T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721610 | |||||||
| chr8:70721650 | C | A | 1 | a0001c0002t0002g0247 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.494-12146C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721650 | |||||||
| chr8:70721721 | A | G | 1 | a0001c0002t0022g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.494-12075A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721721 | |||||||
| chr8:70721731 | C | T | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.494-12065C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721731 | |||||||
| chr8:70721732 | G | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-12064G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721732 | |||||||
| chr8:70721825 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.494-11971G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721825 | |||||||
| chr8:70721938 | C | T | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-11858C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721938 | |||||||
| chr8:70721990 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.494-11806G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721990 | |||||||
| chr8:70722092 | C | CT | 3 | a0001c0001t0003g0054 a0003c0007t0001g0143 a0003c0007t0001g0148 |
3 | NA19062.hp1 NA19062.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.494-11703dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70722092 | ||||||
| chr8:70722125 | A | AT | 8 | a0001c0001t0003g0059 a0001c0001t0003g0067 a0001c0001t0003g0070 others(5): Show |
8 | HG00621.hp1 HG02895.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-11659dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70722125 | ||||||
| chr8:70722223 | A | C | 3 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 |
3 | HG03209.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.494-11573A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722223 | |||||||
| chr8:70722233 | G | C | 4 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0056 others(1): Show |
5 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-11563G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722233 | |||||||
| chr8:70722251 | A | G | 1 | a0001c0001t0018g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.494-11545A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722251 | |||||||
| chr8:70722411 | G | A | 1 | a0001c0002t0022g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.494-11385G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722411 | |||||||
| chr8:70722704 | C | T | 1 | a0001c0005t0006g0093 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.494-11092C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722704 | |||||||
| chr8:70722823 | C | T | 4 | a0001c0001t0004g0044 a0001c0001t0004g0081 a0001c0001t0004g0106 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-10973C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722823 | |||||||
| chr8:70722942 | G | A | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-10854G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722942 | |||||||
| chr8:70722995 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0208 |
3 | HG02074.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.494-10801C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722995 | |||||||
| chr8:70723436 | G | A | 1 | a0001c0001t0004g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.494-10360G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723436 | |||||||
| chr8:70723484 | G | T | 8 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0221 others(5): Show |
10 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-10312G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723484 | |||||||
| chr8:70723564 | C | G | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-10232C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723564 | |||||||
| chr8:70723566 | G | C | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-10230G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723566 | |||||||
| chr8:70723603 | G | A | 1 | a0001c0002t0002g0222 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.494-10193G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723603 | |||||||
| chr8:70723720 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-10076A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723720 | |||||||
| chr8:70723766 | C | A | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-10030C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723766 | |||||||
| chr8:70723766 | C | T | 1 | a0001c0002t0002g0026 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.494-10030C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723766 | |||||||
| chr8:70723772 | C | T | 6 | a0001c0001t0004g0033 a0001c0001t0004g0036 a0001c0001t0004g0037 others(3): Show |
6 | HG00673.hp1 HG01106.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.494-10024C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723772 | |||||||
| chr8:70723793 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.494-10003C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723793 | |||||||
| chr8:70723887 | C | CT | 39 | a0001c0001t0001g0021 a0001c0001t0001g0150 a0001c0001t0001g0161 others(36): Show |
44 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.494-9893dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70723887 | ||||||
| chr8:70723887 | C | CTT | 63 | a0001c0001t0004g0081 a0001c0002t0002g0004 a0001c0002t0002g0010 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-9894_494-9893d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70723887 | ||||||
| chr8:70723887 | C | CTTT | 17 | a0001c0002t0002g0237 a0001c0002t0002g0246 a0001c0002t0002g0270 others(14): Show |
18 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.494-9895_494-9893d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70723887 | ||||||
| chr8:70723899 | T | G | 1 | a0001c0001t0012g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-9897T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723899 | |||||||
| chr8:70723916 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0113 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-9880C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723916 | |||||||
| chr8:70723927 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-9869C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723927 | |||||||
| chr8:70723933 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.494-9863G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723933 | |||||||
| chr8:70723952 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-9844G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723952 | |||||||
| chr8:70723955 | C | T | 1 | a0001c0002t0002g0255 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.494-9841C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723955 | |||||||
| chr8:70723957 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.494-9839T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723957 | |||||||
| chr8:70724103 | G | A | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-9693G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724103 | |||||||
| chr8:70724175 | A | T | 1 | a0001c0001t0004g0041 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.494-9621A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724175 | |||||||
| chr8:70724256 | C | T | 1 | a0001c0001t0004g0036 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.494-9540C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724256 | |||||||
| chr8:70724430 | G | GA | 108 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(105): Show |
128 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.494-9350dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | ||||||
| chr8:70724430 | G | GAA | 9 | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0001g0141 others(6): Show |
9 | HG00642.hp2 HG01081.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.494-9351_494-9350d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | ||||||
| chr8:70724430 | GA | G | 91 | a0001c0001t0004g0013 a0001c0001t0004g0015 a0001c0001t0004g0016 others(88): Show |
104 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.494-9350delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | ||||||
| chr8:70724430 | GAA | G | 16 | a0001c0002t0002g0245 a0001c0002t0005g0023 a0001c0002t0005g0046 others(13): Show |
17 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.494-9351_494-9350d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | ||||||
| chr8:70724515 | G | A | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-9281G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724515 | |||||||
| chr8:70724518 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.494-9278G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724518 | |||||||
| chr8:70724528 | A | T | 1 | a0001c0001t0004g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.494-9268A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724528 | |||||||
| chr8:70724548 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.494-9248C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724548 | |||||||
| chr8:70724554 | G | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-9242G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724554 | |||||||
| chr8:70724607 | C | T | 1 | a0001c0002t0002g0257 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.494-9189C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724607 | |||||||
| chr8:70724619 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.494-9177G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724619 | |||||||
| chr8:70724781 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.494-9015G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724781 | |||||||
| chr8:70724804 | G | A | 1 | a0001c0002t0002g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.494-8992G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724804 | |||||||
| chr8:70724913 | T | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-8883T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724913 | |||||||
| chr8:70724977 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-8819G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724977 | |||||||
| chr8:70725056 | A | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-8740A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725056 | |||||||
| chr8:70725245 | G | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-8551G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725245 | |||||||
| chr8:70725324 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-8472G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725324 | |||||||
| chr8:70725378 | C | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.494-8418C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725378 | |||||||
| chr8:70725487 | GA | G | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-8308delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725487 | |||||||
| chr8:70725528 | G | T | 8 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-8268G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725528 | |||||||
| chr8:70725638 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.494-8158G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725638 | |||||||
| chr8:70725669 | G | C | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-8127G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725669 | |||||||
| chr8:70725760 | G | C | 1 | a0001c0001t0003g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.494-8036G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725760 | |||||||
| chr8:70725773 | G | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-8023G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725773 | |||||||
| chr8:70725779 | G | A | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-8017G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725779 | |||||||
| chr8:70725947 | A | T | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-7849A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725947 | |||||||
| chr8:70726085 | G | A | 2 | a0001c0006t0007g0008 a0001c0006t0007g0080 |
4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-7711G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726085 | |||||||
| chr8:70726216 | G | A | 1 | a0001c0001t0012g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-7580G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726216 | |||||||
| chr8:70726270 | G | T | 1 | a0001c0002t0002g0026 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.494-7526G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726270 | |||||||
| chr8:70726310 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.494-7486C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726310 | |||||||
| chr8:70726311 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.494-7485G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726311 | |||||||
| chr8:70726595 | C | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0169 |
2 | HG01515.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.494-7201C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726595 | |||||||
| chr8:70726727 | C | G | 1 | a0001c0001t0012g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-7069C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726727 | |||||||
| chr8:70726838 | G | A | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-6958G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726838 | |||||||
| chr8:70726948 | C | T | 1 | a0001c0001t0011g0127 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.494-6848C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726948 | |||||||
| chr8:70726988 | TA | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(29): Show |
36 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.494-6801delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70726988 | ||||||
| chr8:70727181 | C | G | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-6615C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727181 | |||||||
| chr8:70727207 | C | G | 2 | a0001c0005t0006g0093 a0001c0005t0006g0115 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.494-6589C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727207 | |||||||
| chr8:70727277 | T | A | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-6519T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727277 | |||||||
| chr8:70727308 | T | C | 1 | a0001c0002t0002g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.494-6488T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727308 | |||||||
| chr8:70727317 | A | T | 1 | a0001c0002t0002g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.494-6479A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727317 | |||||||
| chr8:70727327 | G | GT | 21 | a0001c0001t0001g0022 a0001c0001t0001g0119 a0001c0001t0001g0187 others(18): Show |
22 | HG00738.hp1 HG01891.hp2 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.494-6454dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70727327 | ||||||
| chr8:70727327 | GT | G | 68 | a0001c0001t0001g0156 a0001c0001t0003g0070 a0001c0001t0004g0044 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-6454delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70727327 | ||||||
| chr8:70727327 | GTT | G | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-6455_494-6454d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70727327 | ||||||
| chr8:70727463 | C | T | 1 | a0001c0001t0011g0127 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.494-6333C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727463 | |||||||
| chr8:70727469 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-6327T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727469 | |||||||
| chr8:70727532 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-6264C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727532 | |||||||
| chr8:70727572 | T | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-6224T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727572 | |||||||
| chr8:70727645 | G | A | 2 | a0001c0001t0016g0078 a0001c0001t0017g0031 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.494-6151G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727645 | |||||||
| chr8:70727838 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.494-5958C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727838 | |||||||
| chr8:70728034 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-5762T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728034 | |||||||
| chr8:70728067 | G | A | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-5729G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728067 | |||||||
| chr8:70728179 | G | A | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-5617G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728179 | |||||||
| chr8:70728260 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-5536C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728260 | |||||||
| chr8:70728333 | A | G | 1 | a0001c0002t0002g0269 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.494-5463A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728333 | |||||||
| chr8:70728453 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.494-5343A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728453 | |||||||
| chr8:70728655 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-5141T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728655 | |||||||
| chr8:70728664 | A | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-5132A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728664 | |||||||
| chr8:70728893 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.494-4903G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728893 | |||||||
| chr8:70728961 | A | G | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.494-4835A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728961 | |||||||
| chr8:70729071 | A | G | 1 | a0001c0002t0005g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.494-4725A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729071 | |||||||
| chr8:70729237 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-4559G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729237 | |||||||
| chr8:70729343 | G | A | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-4453G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729343 | |||||||
| chr8:70729408 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-4388T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729408 | |||||||
| chr8:70729413 | G | A | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.494-4383G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729413 | |||||||
| chr8:70729415 | TAGTTC | T | 4 | a0001c0001t0004g0035 a0001c0001t0004g0040 a0001c0001t0004g0041 others(1): Show |
4 | HG01192.hp2 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-4376_494-4372d others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70729415 | ||||||
| chr8:70729554 | GT | G | 5 | a0002c0004t0002g0238 a0002c0004t0009g0216 a0002c0004t0009g0217 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-4238delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70729554 | ||||||
| chr8:70729568 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.494-4228T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729568 | |||||||
| chr8:70729585 | A | C | 5 | a0001c0002t0002g0259 a0001c0002t0002g0260 a0001c0002t0002g0261 others(2): Show |
5 | NA18940.hp1 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-4211A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729585 | |||||||
| chr8:70729608 | A | G | 1 | a0001c0002t0002g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.494-4188A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729608 | |||||||
| chr8:70729647 | G | C | 1 | a0001c0001t0016g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.494-4149G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729647 | |||||||
| chr8:70729657 | C | G | 1 | a0001c0002t0002g0259 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.494-4139C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729657 | |||||||
| chr8:70729826 | G | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-3970G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729826 | |||||||
| chr8:70729915 | A | G | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-3881A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729915 | |||||||
| chr8:70729975 | A | G | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-3821A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729975 | |||||||
| chr8:70730058 | T | C | 1 | a0001c0002t0002g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.494-3738T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730058 | |||||||
| chr8:70730338 | A | G | 116 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(113): Show |
131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.494-3458A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730338 | |||||||
| chr8:70730387 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.494-3409T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730387 | |||||||
| chr8:70730430 | T | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0208 |
3 | HG02074.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.494-3366T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730430 | |||||||
| chr8:70730577 | A | AT | 18 | a0001c0001t0017g0031 a0001c0002t0005g0023 a0001c0002t0005g0046 others(15): Show |
19 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.494-3209dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70730577 | ||||||
| chr8:70730587 | T | TA | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-3206dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70730587 | ||||||
| chr8:70730612 | G | A | 24 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0016 others(21): Show |
27 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.494-3184G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730612 | |||||||
| chr8:70730665 | G | A | 1 | a0001c0002t0002g0010 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.494-3131G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730665 | |||||||
| chr8:70730713 | G | T | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-3083G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730713 | |||||||
| chr8:70730774 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-3022T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730774 | |||||||
| chr8:70730816 | C | G | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-2980C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730816 | |||||||
| chr8:70730888 | G | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-2908G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730888 | |||||||
| chr8:70731107 | C | T | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-2689C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731107 | |||||||
| chr8:70731174 | A | G | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-2622A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731174 | |||||||
| chr8:70731185 | C | A | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-2611C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731185 | |||||||
| chr8:70731324 | C | CT | 80 | a0001c0001t0016g0078 a0001c0002t0002g0004 a0001c0002t0002g0010 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-2462dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70731324 | ||||||
| chr8:70731416 | G | A | 1 | a0001c0002t0005g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.494-2380G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731416 | |||||||
| chr8:70731562 | C | T | 4 | a0001c0002t0008g0215 a0001c0002t0008g0249 a0001c0002t0008g0250 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-2234C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731562 | |||||||
| chr8:70731666 | G | T | 1 | a0005c0009t0004g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-2130G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731666 | |||||||
| chr8:70731788 | G | C | 12 | a0001c0002t0005g0023 a0001c0002t0005g0046 a0001c0002t0005g0209 others(9): Show |
13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-2008G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731788 | |||||||
| chr8:70731809 | T | C | 2 | a0001c0001t0004g0044 a0001c0001t0004g0106 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-1987T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731809 | |||||||
| chr8:70731872 | C | T | 1 | a0001c0003t0003g0073 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.494-1924C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731872 | |||||||
| chr8:70732016 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.494-1780G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732016 | |||||||
| chr8:70732068 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.494-1728G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732068 | |||||||
| chr8:70732110 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.494-1686C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732110 | |||||||
| chr8:70732221 | A | G | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-1575A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732221 | |||||||
| chr8:70732239 | C | T | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-1557C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732239 | |||||||
| chr8:70732301 | A | G | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-1495A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732301 | |||||||
| chr8:70732493 | C | T | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-1303C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732493 | |||||||
| chr8:70732531 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.494-1265C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732531 | |||||||
| chr8:70732572 | T | C | 114 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(111): Show |
129 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.494-1224T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732572 | |||||||
| chr8:70732786 | G | A | 1 | a0002c0004t0002g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-1010G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732786 | |||||||
| chr8:70732845 | C | T | 4 | a0002c0004t0009g0216 a0002c0004t0009g0217 a0002c0004t0009g0218 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-951C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732845 | |||||||
| chr8:70732921 | C | G | 68 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(65): Show |
78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-875C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732921 | |||||||
| chr8:70732937 | G | A | 1 | a0001c0003t0003g0058 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.494-859G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732937 | |||||||
| chr8:70732968 | G | A | 176 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(173): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.494-828G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732968 | |||||||
| chr8:70732982 | G | C | 36 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0015 others(33): Show |
40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-814G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732982 | |||||||
| chr8:70733033 | G | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-763G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733033 | |||||||
| chr8:70733119 | A | G | 2 | a0001c0001t0013g0087 a0001c0001t0013g0094 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.494-677A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733119 | |||||||
| chr8:70733389 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.494-407A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733389 | |||||||
| chr8:70733418 | G | T | 3 | a0001c0001t0011g0116 a0001c0001t0011g0127 a0001c0001t0011g0201 |
3 | HG02132.hp1 NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.494-378G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733418 | |||||||
| chr8:70733492 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.494-304A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733492 | |||||||
| chr8:70733625 | T | C | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-171T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733625 | |||||||
| chr8:70733636 | C | T | 80 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(77): Show |
91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.494-160C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733636 | |||||||
| chr8:70733691 | C | T | 63 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.494-105C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733691 |