Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1659 |
| ensemblid | ENSG00000067596.12 |
| hgncid | 2749 |
| symbol | DHX8 |
| name | DEAH-box helicase 8 |
| refseq_nuc | NM_004941.3 |
| refseq_prot | NP_004932.1 |
| ensembl_nuc | ENST00000262415.8 |
| ensembl_prot | ENSP00000262415.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 43483975 |
| end | 43525670 |
| strand | + |
| ver | v1.2 |
| region | chr17:43483975-43525670 |
| region5000 | chr17:43478975-43530670 |
| regionname0 | DHX8_chr17_43483975_43525670 |
| regionname5000 | DHX8_chr17_43478975_43530670 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1220 | 351 | 76 | 64 | 151 | 14 | 44 | 121 | DHX8_chr17_43478975_43530670 | DHX8 | MAVAV others(1215): Show |
chr17 | 43478975 | 43530670 |
| a0002 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | MAVAV others(1215): Show |
chr17 | 43478975 | 43530670 |
| a0003 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | MAVAV others(1215): Show |
chr17 | 43478975 | 43530670 |
| a0004 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | MAVAV others(1215): Show |
chr17 | 43478975 | 43530670 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3660 | 347 | 74 | 64 | 150 | 14 | 43 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 | ||
| a0001c0002 | 0/0 | 3660 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 | ||
| a0001c0003 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 | ||
| a0001c0006 | 0/0 | 3660 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 | ||
| a0002c0005 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 | ||
| a0003c0004 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 | ||
| a0004c0007 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | ATGGC others(3655): Show |
chr17 | 43478975 | 43530670 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5549 | 106 | 7 | 26 | 47 | 5 | 19 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0002 | 0/0 | 5549 | 98 | 18 | 17 | 48 | 4 | 11 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0003 | 0/0 | 5549 | 96 | 20 | 16 | 46 | 4 | 10 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0004 | 0/0 | 5549 | 11 | 11 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0005 | 0/0 | 5550 | 6 | 0 | 2 | 3 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0006 | 0/0 | 5549 | 4 | 4 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0007 | 0/0 | 5550 | 5 | 0 | 0 | 4 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0008 | 0/0 | 5549 | 5 | 5 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0009 | 0/0 | 5550 | 3 | 0 | 1 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0010 | 0/0 | 5549 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0011 | 0/0 | 5549 | 2 | 0 | 0 | 0 | 0 | 2 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0012 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0013 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0014 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0015 | 0/0 | 5549 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0016 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0017 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0018 | 0/0 | 5549 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0019 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0001c0001t0020 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0002t0006 | 0/0 | 5549 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0001c0003t0005 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0001c0006t0007 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5545): Show |
chr17 | 43478975 | 43530670 |
| a0002c0005t0002 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0003c0004t0002 | 0/0 | 5549 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| a0004c0007t0001 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | AACCC others(5544): Show |
chr17 | 43478975 | 43530670 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 1 | 1 | 4 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0001g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0001 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0009g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0014g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0015g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0016g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0017g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0018g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0019g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0002t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0002t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0001c0006t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0002c0005t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0003c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| a0004c0007t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | GBR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | FIN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | FIN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0220 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00733 | hp1 | a0001 | c0001 | t0015 | g0074 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0044 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0130 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0284 | EUR | IBS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0025 | EUR | IBS | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0267 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01928 | hp2 | a0001 | c0001 | t0018 | g0087 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0269 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | CDX | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | CDX | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0127 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0247 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0282 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0262 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0256 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03098 | hp1 | a0002 | c0005 | t0002 | g0105 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0266 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0265 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03225 | hp2 | a0001 | c0002 | t0006 | g0012 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0254 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0104 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0252 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0250 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03654 | hp1 | a0001 | c0006 | t0007 | g0175 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0002 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0163 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0249 | SAS | STU | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0255 | AFR | YRI | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | YRI | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18940 | hp2 | a0003 | c0004 | t0002 | g0090 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0165 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0084 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | LWK | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0113 | AFR | LWK | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | LWK | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19087 | hp1 | a0001 | c0003 | t0005 | g0195 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19240 | hp1 | a0004 | c0007 | t0001 | g0132 | AFR | YRI | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | YRI | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ASW | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ASW | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | TSI | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | USA | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | USA | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0139 | REF | REF | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0277 | REF | REF | DHX8_chr17_43478975_43530670 | DHX8 | chr17 | 43478975 | 43530670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43484152 | G | A | 1 | a0003 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.115G>A | p.Asp39Asn | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/23 | 178/5549 | 115/3663 | 39/1220 | chr17 | 43484152 | |||
| chr17:43492229 | A | G | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.440A>G | p.Lys147Arg | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 5/23 | 503/5549 | 440/3663 | 147/1220 | chr17 | 43492229 | |||
| chr17:43493879 | T | C | 1 | a0002 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1205T>C | p.Ile402Thr | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/23 | 1268/5549 | 1205/3663 | 402/1220 | chr17 | 43493879 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43484049 | T | G | 1 | a0001c0003 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.12T>G | p.Ala4Ala | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/23 | 75/5549 | 12/3663 | 4/1220 | chr17 | 43484049 | |||
| chr17:43490456 | T | A | 1 | a0001c0002 | 2 | HG03225.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.300T>A | p.Thr100Thr | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 3/23 | 363/5549 | 300/3663 | 100/1220 | chr17 | 43490456 | |||
| chr17:43520864 | C | G | 1 | a0001c0006 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.3051C>G | p.Val1017Val | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/23 | 3114/5549 | 3051/3663 | 1017/1220 | chr17 | 43520864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43524002 | T | C | 1 | a0001c0001t0010 | 2 | HG03209.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*155T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 155 | chr17 | 43524002 | ||||||
| chr17:43524254 | C | T | 2 | a0001c0001t0004 a0001c0001t0020 |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*407C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 407 | chr17 | 43524254 | ||||||
| chr17:43524451 | G | A | 1 | a0001c0001t0012 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 604 | chr17 | 43524451 | ||||||
| chr17:43524543 | A | G | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(13): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*696A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 696 | chr17 | 43524543 | ||||||
| chr17:43524544 | C | T | 1 | a0001c0001t0019 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 697 | chr17 | 43524544 | ||||||
| chr17:43524624 | A | G | 1 | a0001c0001t0018 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*777A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 777 | chr17 | 43524624 | ||||||
| chr17:43524733 | T | A | 1 | a0001c0001t0013 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*886T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 886 | chr17 | 43524733 | ||||||
| chr17:43524771 | A | G | 1 | a0001c0001t0010 | 2 | HG03209.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*924A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 924 | chr17 | 43524771 | ||||||
| chr17:43524956 | G | GT | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0009 others(4): Show |
18 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1121dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1122 | INFO_REALIGN_3_PRIME | chr17 | 43524956 | |||||
| chr17:43525142 | C | T | 1 | a0001c0001t0011 | 2 | HG03704.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1295C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1295 | chr17 | 43525142 | ||||||
| chr17:43525150 | G | A | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(3): Show |
110 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1303G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1303 | chr17 | 43525150 | ||||||
| chr17:43525193 | G | T | 2 | a0001c0001t0010 a0001c0001t0016 |
3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1346G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1346 | chr17 | 43525193 | ||||||
| chr17:43525285 | A | G | 1 | a0001c0001t0020 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1438A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1438 | chr17 | 43525285 | ||||||
| chr17:43525390 | A | G | 2 | a0001c0001t0006 a0001c0002t0006 |
6 | HG02809.hp2 HG03225.hp2 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1543 | chr17 | 43525390 | ||||||
| chr17:43525395 | G | A | 1 | a0001c0001t0015 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1548 | chr17 | 43525395 | ||||||
| chr17:43525400 | C | T | 4 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0017 others(1): Show |
8 | HG02895.hp1 HG03041.hp2 HG03130.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1553C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1553 | chr17 | 43525400 | ||||||
| chr17:43525490 | T | G | 10 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(7): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1643T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1643 | chr17 | 43525490 | ||||||
| chr17:43525497 | T | C | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0015 others(3): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1650T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 23/23 | 1650 | chr17 | 43525497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43484200 | G | GT | 3 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0001t0003g0287 |
3 | HG02258.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.148+16dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43484200 | ||||||
| chr17:43484233 | CGGAAGGA | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.148+64_148+70delGA others(5): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43484233 | ||||||
| chr17:43484296 | GTC | G | 13 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(10): Show |
15 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.148+119_148+120del others(2): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43484296 | ||||||
| chr17:43484309 | G | T | 1 | a0001c0001t0003g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.148+124G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484309 | |||||||
| chr17:43484315 | A | C | 1 | a0001c0001t0002g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.148+130A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484315 | |||||||
| chr17:43484318 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.148+133G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484318 | |||||||
| chr17:43484423 | G | T | 1 | a0001c0001t0008g0262 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.148+238G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484423 | |||||||
| chr17:43484627 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.148+442T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484627 | |||||||
| chr17:43484673 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.148+488G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484673 | |||||||
| chr17:43484676 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.148+491C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484676 | |||||||
| chr17:43484687 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.148+502G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484687 | |||||||
| chr17:43484849 | C | A | 1 | a0001c0001t0002g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.148+664C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484849 | |||||||
| chr17:43484899 | T | A | 1 | a0001c0001t0002g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.148+714T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484899 | |||||||
| chr17:43484918 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.148+733C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484918 | |||||||
| chr17:43484996 | G | A | 3 | a0001c0001t0010g0265 a0001c0001t0010g0266 a0001c0001t0016g0267 |
3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.148+811G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43484996 | |||||||
| chr17:43485104 | A | C | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+919A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485104 | |||||||
| chr17:43485105 | T | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(91): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.148+920T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485105 | |||||||
| chr17:43485168 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.148+983T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485168 | |||||||
| chr17:43485174 | T | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.148+989T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485174 | |||||||
| chr17:43485410 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.148+1225T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485410 | |||||||
| chr17:43485548 | G | A | 5 | a0001c0001t0003g0021 a0001c0001t0003g0114 a0001c0001t0003g0115 others(2): Show |
6 | HG01070.hp1 HG01346.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+1363G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485548 | |||||||
| chr17:43485783 | G | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(87): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.148+1598G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485783 | |||||||
| chr17:43485857 | A | G | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.148+1672A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485857 | |||||||
| chr17:43485935 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.148+1750G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485935 | |||||||
| chr17:43485962 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.148+1777C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43485962 | |||||||
| chr17:43486076 | T | TGCCTGTA others(6): Show |
94 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(91): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.148+1893_148+1894i others(15): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43486076 | ||||||
| chr17:43486163 | C | T | 1 | a0001c0001t0003g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.148+1978C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486163 | |||||||
| chr17:43486192 | A | G | 2 | a0001c0001t0008g0255 a0001c0001t0008g0256 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.148+2007A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486192 | |||||||
| chr17:43486598 | G | A | 2 | a0001c0001t0003g0121 a0001c0001t0003g0122 |
2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.148+2413G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486598 | |||||||
| chr17:43486629 | C | T | 92 | a0001c0001t0001g0216 a0001c0001t0003g0006 a0001c0001t0003g0010 others(89): Show |
105 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.148+2444C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486629 | |||||||
| chr17:43486659 | TC | T | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.148+2475delC | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486659 | |||||||
| chr17:43486677 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.148+2492G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486677 | |||||||
| chr17:43486707 | T | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | NA18939.hp1 NA18974.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+2522T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486707 | |||||||
| chr17:43486875 | C | CA | 88 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(85): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.149-2556dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43486875 | ||||||
| chr17:43486875 | CA | C | 28 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0188 others(25): Show |
29 | HG01256.hp1 HG01515.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.149-2556delA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43486875 | ||||||
| chr17:43486925 | T | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(105): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.149-2524T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486925 | |||||||
| chr17:43486932 | G | A | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.149-2517G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43486932 | |||||||
| chr17:43487090 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.149-2359G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487090 | |||||||
| chr17:43487114 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.149-2335G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487114 | |||||||
| chr17:43487158 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.149-2291A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487158 | |||||||
| chr17:43487593 | A | G | 4 | a0001c0001t0010g0265 a0001c0001t0010g0266 a0001c0001t0013g0127 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-1856A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487593 | |||||||
| chr17:43487837 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.149-1612C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487837 | |||||||
| chr17:43487909 | G | A | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-1540G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487909 | |||||||
| chr17:43487972 | T | TA | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-1468dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43487972 | ||||||
| chr17:43487981 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.149-1468A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43487981 | |||||||
| chr17:43488007 | C | T | 1 | a0001c0001t0004g0275 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.149-1442C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488007 | |||||||
| chr17:43488067 | C | T | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-1382C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488067 | |||||||
| chr17:43488068 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.149-1381G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488068 | |||||||
| chr17:43488075 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.149-1374C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488075 | |||||||
| chr17:43488137 | T | G | 89 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(86): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-1312T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488137 | |||||||
| chr17:43488245 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.149-1204T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488245 | |||||||
| chr17:43488254 | G | C | 3 | a0001c0001t0004g0268 a0001c0001t0004g0270 a0001c0001t0020g0269 |
3 | HG02055.hp2 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.149-1195G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488254 | |||||||
| chr17:43488273 | G | A | 1 | a0001c0003t0005g0195 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.149-1176G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488273 | |||||||
| chr17:43488277 | CAAAAAAA others(4): Show |
C | 14 | a0001c0001t0003g0011 a0001c0001t0003g0229 a0001c0001t0003g0230 others(11): Show |
16 | HG00639.hp1 HG01261.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.149-1155_149-1145d others(13): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43488277 | ||||||
| chr17:43488288 | AAAAAAAA others(2): Show |
A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(86): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-1153_149-1145d others(11): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43488288 | ||||||
| chr17:43488296 | AG | A | 14 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(11): Show |
16 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-1152delG | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488296 | |||||||
| chr17:43488297 | G | A | 4 | a0001c0001t0008g0255 a0001c0001t0008g0257 a0001c0001t0008g0258 others(1): Show |
4 | HG03130.hp1 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.149-1152G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488297 | |||||||
| chr17:43488333 | C | A | 1 | a0001c0001t0002g0041 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.149-1116C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488333 | |||||||
| chr17:43488463 | T | A | 3 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 |
3 | NA18985.hp1 NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.149-986T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488463 | |||||||
| chr17:43488471 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.149-978C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488471 | |||||||
| chr17:43488610 | T | TA | 15 | a0001c0001t0001g0260 a0001c0001t0003g0006 a0001c0001t0003g0021 others(12): Show |
19 | HG01070.hp1 HG01346.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-825dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43488610 | ||||||
| chr17:43488610 | T | TAA | 85 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(82): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.149-826_149-825dup others(2): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43488610 | ||||||
| chr17:43488814 | G | A | 1 | a0001c0001t0008g0262 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.149-635G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488814 | |||||||
| chr17:43488862 | A | C | 1 | a0001c0001t0003g0241 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.149-587A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488862 | |||||||
| chr17:43488979 | A | G | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.149-470A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43488979 | |||||||
| chr17:43489013 | G | GT | 7 | a0001c0001t0001g0126 a0001c0001t0001g0187 a0001c0001t0002g0099 others(4): Show |
7 | HG00140.hp2 HG02080.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-427dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43489013 | ||||||
| chr17:43489014 | T | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.149-435T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43489014 | |||||||
| chr17:43489128 | C | T | 1 | a0001c0001t0003g0228 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.149-321C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43489128 | |||||||
| chr17:43489194 | G | A | 1 | a0001c0001t0012g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149-255G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43489194 | |||||||
| chr17:43489268 | G | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(86): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-181G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43489268 | |||||||
| chr17:43489374 | T | C | 1 | a0001c0001t0009g0044 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.149-75T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | chr17 | 43489374 | |||||||
| chr17:43489415 | CTCT | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.149-29_149-27delCT others(1): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 43489415 | ||||||
| chr17:43489542 | T | TATGTGGA others(97): Show |
2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.234+66_234+67insGT others(102): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 43489542 | ||||||
| chr17:43489601 | T | G | 90 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(87): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.234+67T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489601 | |||||||
| chr17:43489685 | G | A | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.234+151G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489685 | |||||||
| chr17:43489751 | C | T | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+217C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489751 | |||||||
| chr17:43489780 | T | C | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.234+246T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489780 | |||||||
| chr17:43489842 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.234+308G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489842 | |||||||
| chr17:43489853 | G | A | 1 | a0001c0001t0017g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+319G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489853 | |||||||
| chr17:43489883 | G | A | 1 | a0001c0001t0004g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234+349G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489883 | |||||||
| chr17:43489911 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+377G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43489911 | |||||||
| chr17:43490034 | C | CCT | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.235-354_235-353dup others(2): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 43490034 | ||||||
| chr17:43490275 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0129 others(5): Show |
10 | HG00738.hp1 HG01106.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-116A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 2/22 | chr17 | 43490275 | |||||||
| chr17:43490960 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.308-205C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 3/22 | chr17 | 43490960 | |||||||
| chr17:43491141 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
9 | HG02083.hp2 HG02165.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-24C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 3/22 | chr17 | 43491141 | |||||||
| chr17:43491314 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.393+64C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491314 | |||||||
| chr17:43491326 | A | T | 1 | a0001c0001t0002g0097 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.393+76A>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491326 | |||||||
| chr17:43491426 | T | C | 1 | a0001c0001t0008g0262 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.393+176T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491426 | |||||||
| chr17:43491456 | G | A | 2 | a0001c0001t0010g0265 a0001c0001t0010g0266 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.393+206G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491456 | |||||||
| chr17:43491527 | A | AT | 80 | a0001c0001t0001g0186 a0001c0001t0002g0001 a0001c0001t0002g0007 others(77): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.393+289dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 43491527 | ||||||
| chr17:43491527 | A | ATT | 6 | a0001c0001t0002g0020 a0001c0001t0002g0092 a0001c0001t0002g0093 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+288_393+289dup others(2): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 43491527 | ||||||
| chr17:43491657 | C | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.393+407C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491657 | |||||||
| chr17:43491690 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.393+440T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491690 | |||||||
| chr17:43491973 | A | G | 14 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(11): Show |
16 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-210A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43491973 | |||||||
| chr17:43492016 | A | G | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-167A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43492016 | |||||||
| chr17:43492092 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-91A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43492092 | |||||||
| chr17:43492165 | C | T | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.394-18C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 4/22 | chr17 | 43492165 | |||||||
| chr17:43492565 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.504-116C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 5/22 | chr17 | 43492565 | |||||||
| chr17:43493059 | T | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.863+19T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 6/22 | chr17 | 43493059 | |||||||
| chr17:43493413 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.864-32G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 6/22 | chr17 | 43493413 | |||||||
| chr17:43493900 | G | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0189 |
2 | HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1212+14G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43493900 | |||||||
| chr17:43494115 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1212+229G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494115 | |||||||
| chr17:43494209 | G | A | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(88): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1212+323G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494209 | |||||||
| chr17:43494310 | C | G | 1 | a0001c0001t0017g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1212+424C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494310 | |||||||
| chr17:43494503 | C | T | 2 | a0001c0001t0010g0265 a0001c0001t0010g0266 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1212+617C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494503 | |||||||
| chr17:43494593 | C | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1212+707C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494593 | |||||||
| chr17:43494619 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1212+733G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494619 | |||||||
| chr17:43494646 | G | A | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1212+760G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494646 | |||||||
| chr17:43494720 | C | CA | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0190 others(9): Show |
12 | HG02083.hp1 HG02135.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1212+852dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr17 | 43494720 | ||||||
| chr17:43494720 | CA | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
9 | HG02083.hp2 HG02165.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1212+852delA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr17 | 43494720 | ||||||
| chr17:43494809 | CT | C | 83 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(80): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1212+939delT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr17 | 43494809 | ||||||
| chr17:43494809 | CTT | C | 9 | a0001c0001t0002g0007 a0001c0001t0002g0048 a0001c0001t0002g0106 others(6): Show |
11 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212+938_1212+939d others(4): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr17 | 43494809 | ||||||
| chr17:43494867 | A | G | 1 | a0001c0001t0017g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1212+981A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494867 | |||||||
| chr17:43494875 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212+989G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494875 | |||||||
| chr17:43494905 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1212+1019G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494905 | |||||||
| chr17:43494915 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1212+1029G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494915 | |||||||
| chr17:43494939 | G | A | 41 | a0001c0001t0001g0216 a0001c0001t0003g0010 a0001c0001t0003g0011 others(38): Show |
46 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1212+1053G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494939 | |||||||
| chr17:43494956 | C | T | 1 | a0001c0001t0003g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1212+1070C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43494956 | |||||||
| chr17:43494978 | A | AT | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1212+1099dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr17 | 43494978 | ||||||
| chr17:43495094 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1213-1087G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43495094 | |||||||
| chr17:43495418 | T | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1213-763T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43495418 | |||||||
| chr17:43495719 | A | G | 3 | a0001c0001t0008g0257 a0001c0001t0008g0258 a0001c0001t0017g0254 |
3 | HG03130.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1213-462A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43495719 | |||||||
| chr17:43495889 | A | G | 1 | a0001c0001t0008g0262 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1213-292A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43495889 | |||||||
| chr17:43495971 | G | A | 8 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
10 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1213-210G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43495971 | |||||||
| chr17:43496023 | A | C | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1213-158A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43496023 | |||||||
| chr17:43496159 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0140 a0001c0001t0001g0181 others(4): Show |
7 | HG00642.hp1 HG01106.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1213-22C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 8/22 | chr17 | 43496159 | |||||||
| chr17:43496362 | T | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1300+94T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43496362 | |||||||
| chr17:43496459 | A | G | 1 | a0001c0001t0014g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1300+191A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43496459 | |||||||
| chr17:43496486 | A | G | 14 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(11): Show |
16 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1300+218A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43496486 | |||||||
| chr17:43496729 | G | A | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300+461G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43496729 | |||||||
| chr17:43496777 | C | CA | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1300+520dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr17 | 43496777 | ||||||
| chr17:43496938 | T | A | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1300+670T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43496938 | |||||||
| chr17:43497026 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1300+758T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497026 | |||||||
| chr17:43497103 | C | G | 1 | a0001c0001t0008g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1300+835C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497103 | |||||||
| chr17:43497270 | TTCAC | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1300+1008_1300+101 others(8): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr17 | 43497270 | ||||||
| chr17:43497282 | T | C | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(88): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1300+1014T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497282 | |||||||
| chr17:43497445 | C | T | 2 | a0001c0001t0003g0280 a0001c0001t0003g0281 |
2 | HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1300+1177C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497445 | |||||||
| chr17:43497475 | A | C | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1300+1207A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497475 | |||||||
| chr17:43497722 | T | C | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0049 others(2): Show |
5 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1301-1140T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497722 | |||||||
| chr17:43497748 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0109 a0001c0001t0002g0110 others(2): Show |
7 | HG02257.hp2 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1301-1114C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497748 | |||||||
| chr17:43497842 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1301-1020G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497842 | |||||||
| chr17:43497896 | C | T | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(3): Show |
6 | HG02080.hp1 NA18942.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1301-966C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497896 | |||||||
| chr17:43497962 | G | C | 1 | a0001c0001t0020g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1301-900G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43497962 | |||||||
| chr17:43498044 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1301-818G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498044 | |||||||
| chr17:43498078 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1301-784T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498078 | |||||||
| chr17:43498138 | G | GT | 6 | a0001c0001t0002g0047 a0001c0001t0002g0088 a0001c0001t0002g0089 others(3): Show |
6 | HG00140.hp2 HG01928.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1301-723dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr17 | 43498138 | ||||||
| chr17:43498140 | G | T | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1301-722G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498140 | |||||||
| chr17:43498393 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1301-469C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498393 | |||||||
| chr17:43498443 | G | A | 1 | a0001c0001t0003g0028 | 2 | HG01943.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1301-419G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498443 | |||||||
| chr17:43498679 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1301-183C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498679 | |||||||
| chr17:43498680 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1301-182C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498680 | |||||||
| chr17:43498702 | G | C | 1 | a0001c0001t0003g0207 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1301-160G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498702 | |||||||
| chr17:43498737 | C | T | 2 | a0001c0001t0008g0255 a0001c0001t0008g0256 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1301-125C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 9/22 | chr17 | 43498737 | |||||||
| chr17:43499041 | G | A | 1 | a0001c0001t0008g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1398+82G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 10/22 | chr17 | 43499041 | |||||||
| chr17:43499456 | G | A | 2 | a0001c0001t0008g0255 a0001c0001t0008g0256 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1398+497G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 10/22 | chr17 | 43499456 | |||||||
| chr17:43499609 | G | T | 1 | a0001c0006t0007g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1399-347G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 10/22 | chr17 | 43499609 | |||||||
| chr17:43499690 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1399-266C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 10/22 | chr17 | 43499690 | |||||||
| chr17:43499904 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0091 |
3 | HG02735.hp1 HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1399-52A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 10/22 | chr17 | 43499904 | |||||||
| chr17:43500201 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1546+98T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43500201 | |||||||
| chr17:43500464 | G | A | 7 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0271 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+361G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43500464 | |||||||
| chr17:43500629 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1546+526G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43500629 | |||||||
| chr17:43500641 | C | T | 25 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(22): Show |
29 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.1546+538C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43500641 | |||||||
| chr17:43500661 | C | T | 14 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(11): Show |
16 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546+558C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43500661 | |||||||
| chr17:43500784 | G | A | 2 | a0001c0001t0010g0265 a0001c0001t0010g0266 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1546+681G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43500784 | |||||||
| chr17:43501102 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1546+999C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43501102 | |||||||
| chr17:43501129 | C | T | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(105): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1546+1026C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43501129 | |||||||
| chr17:43501506 | A | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(105): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1546+1403A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43501506 | |||||||
| chr17:43501633 | A | G | 218 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0129 others(215): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1546+1530A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43501633 | |||||||
| chr17:43501725 | TC | T | 90 | a0001c0001t0001g0150 a0001c0001t0002g0001 a0001c0001t0002g0007 others(87): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1546+1631delC | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr17 | 43501725 | ||||||
| chr17:43501919 | A | G | 92 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(89): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1546+1816A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43501919 | |||||||
| chr17:43502115 | C | T | 3 | a0001c0001t0003g0226 a0001c0001t0003g0286 a0001c0001t0003g0287 |
3 | HG02258.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1546+2012C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502115 | |||||||
| chr17:43502230 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1546+2127T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502230 | |||||||
| chr17:43502249 | T | G | 1 | a0001c0001t0009g0044 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1546+2146T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502249 | |||||||
| chr17:43502280 | T | C | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG01361.hp1 HG01433.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2177T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502280 | |||||||
| chr17:43502395 | T | C | 3 | a0001c0001t0004g0268 a0001c0001t0004g0270 a0001c0001t0020g0269 |
3 | HG02055.hp2 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1547-2249T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502395 | |||||||
| chr17:43502535 | C | T | 3 | a0001c0001t0003g0226 a0001c0001t0003g0286 a0001c0001t0003g0287 |
3 | HG02258.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1547-2109C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502535 | |||||||
| chr17:43502549 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1547-2095A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502549 | |||||||
| chr17:43502616 | C | T | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1547-2028C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502616 | |||||||
| chr17:43502669 | G | T | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-1975G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502669 | |||||||
| chr17:43502713 | C | T | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
4 | HG00280.hp2 HG00735.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-1931C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43502713 | |||||||
| chr17:43503181 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1547-1463G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503181 | |||||||
| chr17:43503220 | A | G | 93 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(90): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1547-1424A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503220 | |||||||
| chr17:43503453 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1547-1191C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503453 | |||||||
| chr17:43503492 | C | T | 1 | a0001c0001t0013g0127 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1547-1152C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503492 | |||||||
| chr17:43503503 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1547-1141A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503503 | |||||||
| chr17:43503523 | T | G | 92 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(89): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1547-1121T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503523 | |||||||
| chr17:43503595 | G | T | 1 | a0001c0001t0004g0270 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1547-1049G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503595 | |||||||
| chr17:43503620 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1547-1024G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503620 | |||||||
| chr17:43503744 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1547-900G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43503744 | |||||||
| chr17:43504177 | T | C | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1547-467T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43504177 | |||||||
| chr17:43504305 | T | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1547-339T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43504305 | |||||||
| chr17:43504346 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1547-298A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43504346 | |||||||
| chr17:43504437 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1547-207G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43504437 | |||||||
| chr17:43504565 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1547-79C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 11/22 | chr17 | 43504565 | |||||||
| chr17:43504907 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1728+82G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43504907 | |||||||
| chr17:43504916 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1728+91A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43504916 | |||||||
| chr17:43505003 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1728+178G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505003 | |||||||
| chr17:43505004 | C | T | 2 | a0001c0001t0010g0265 a0001c0001t0010g0266 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1728+179C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505004 | |||||||
| chr17:43505271 | T | C | 1 | a0001c0001t0017g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1728+446T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505271 | |||||||
| chr17:43505328 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1728+503G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505328 | |||||||
| chr17:43505365 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1728+540C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505365 | |||||||
| chr17:43505427 | G | A | 5 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(2): Show |
5 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1728+602G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505427 | |||||||
| chr17:43505593 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1728+768A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43505593 | |||||||
| chr17:43506125 | T | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1729-878T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506125 | |||||||
| chr17:43506143 | A | G | 1 | a0001c0001t0003g0201 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1729-860A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506143 | |||||||
| chr17:43506197 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1729-806G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506197 | |||||||
| chr17:43506244 | A | C | 1 | a0001c0001t0003g0193 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1729-759A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506244 | |||||||
| chr17:43506322 | CAA | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
10 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1729-674_1729-673d others(4): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 43506322 | ||||||
| chr17:43506417 | G | C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0232 a0001c0001t0003g0233 others(3): Show |
8 | HG00639.hp1 HG01261.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1729-586G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506417 | |||||||
| chr17:43506636 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1729-367C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506636 | |||||||
| chr17:43506848 | A | G | 7 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(4): Show |
7 | HG02280.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1729-155A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506848 | |||||||
| chr17:43506854 | A | G | 4 | a0001c0001t0008g0257 a0001c0001t0008g0258 a0001c0001t0017g0254 others(1): Show |
4 | HG03130.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1729-149A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506854 | |||||||
| chr17:43506999 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18940.hp1 | splice_region_variant&intron_variant | LOW | c.1729-4T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 12/22 | chr17 | 43506999 | |||||||
| chr17:43507251 | C | G | 1 | a0001c0001t0003g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1923+54C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 13/22 | chr17 | 43507251 | |||||||
| chr17:43507359 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1924-144A>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 13/22 | chr17 | 43507359 | |||||||
| chr17:43507393 | T | G | 1 | a0001c0001t0002g0101 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1924-110T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 13/22 | chr17 | 43507393 | |||||||
| chr17:43507441 | G | C | 1 | a0001c0001t0008g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1924-62G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 13/22 | chr17 | 43507441 | |||||||
| chr17:43507742 | A | C | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2109+54A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 14/22 | chr17 | 43507742 | |||||||
| chr17:43508219 | C | T | 8 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
10 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2321-120C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 15/22 | chr17 | 43508219 | |||||||
| chr17:43508289 | G | A | 204 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(201): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2321-50G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 15/22 | chr17 | 43508289 | |||||||
| chr17:43508555 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2502+35T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508555 | |||||||
| chr17:43508618 | C | CT | 11 | a0001c0001t0001g0169 a0001c0001t0002g0046 a0001c0001t0002g0073 others(8): Show |
11 | HG00733.hp1 HG02135.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2502+115dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43508618 | ||||||
| chr17:43508658 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2502+138C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508658 | |||||||
| chr17:43508713 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2502+193G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508713 | |||||||
| chr17:43508810 | G | A | 1 | a0001c0001t0020g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2502+290G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508810 | |||||||
| chr17:43508813 | G | A | 1 | a0001c0001t0012g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2502+293G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508813 | |||||||
| chr17:43508917 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0272 others(3): Show |
8 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2502+397C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508917 | |||||||
| chr17:43508933 | C | A | 3 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0073 |
3 | NA18994.hp1 NA19010.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2502+413C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43508933 | |||||||
| chr17:43509001 | A | C | 6 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(3): Show |
6 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2502+481A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509001 | |||||||
| chr17:43509085 | G | A | 3 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0275 |
5 | HG02486.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2502+565G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509085 | |||||||
| chr17:43509107 | C | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2502+587C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509107 | |||||||
| chr17:43509150 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2502+630T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509150 | |||||||
| chr17:43509197 | C | G | 6 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(3): Show |
6 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2502+677C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509197 | |||||||
| chr17:43509284 | G | C | 1 | a0001c0001t0003g0228 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2502+764G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509284 | |||||||
| chr17:43509317 | A | G | 204 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(201): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2502+797A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509317 | |||||||
| chr17:43509484 | A | AT | 10 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0002g0096 others(7): Show |
10 | HG00408.hp1 HG02300.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.2502+981dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43509484 | ||||||
| chr17:43509532 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2502+1012G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509532 | |||||||
| chr17:43509580 | C | T | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2502+1060C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509580 | |||||||
| chr17:43509677 | T | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2502+1157T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509677 | |||||||
| chr17:43509678 | T | G | 9 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0107 others(6): Show |
11 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2502+1158T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509678 | |||||||
| chr17:43509749 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2502+1229A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509749 | |||||||
| chr17:43509861 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2502+1341G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509861 | |||||||
| chr17:43509878 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2502+1358G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509878 | |||||||
| chr17:43509889 | G | A | 17 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0020 others(14): Show |
20 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.2502+1369G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43509889 | |||||||
| chr17:43510033 | T | TTTTG | 27 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0144 others(24): Show |
35 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.2502+1541_2502+154 others(8): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43510033 | ||||||
| chr17:43510070 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2502+1550T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510070 | |||||||
| chr17:43510097 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2502+1577G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510097 | |||||||
| chr17:43510167 | G | A | 1 | a0001c0001t0012g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2502+1647G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510167 | |||||||
| chr17:43510250 | T | G | 204 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(201): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2502+1730T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510250 | |||||||
| chr17:43510459 | G | A | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2502+1939G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510459 | |||||||
| chr17:43510489 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2502+1969A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510489 | |||||||
| chr17:43510523 | A | G | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2502+2003A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510523 | |||||||
| chr17:43510548 | T | G | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2502+2028T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510548 | |||||||
| chr17:43510587 | T | G | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2502+2067T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510587 | |||||||
| chr17:43510683 | C | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0108 a0001c0001t0002g0109 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2502+2163C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43510683 | |||||||
| chr17:43511191 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2503-2171G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43511191 | |||||||
| chr17:43511234 | A | G | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2503-2128A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43511234 | |||||||
| chr17:43511456 | A | ATTTTTTT others(4): Show |
7 | a0001c0001t0002g0041 a0001c0001t0002g0054 a0001c0001t0002g0263 others(4): Show |
7 | HG02055.hp2 HG02698.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2503-1897_2503-188 others(15): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(5): Show |
43 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(40): Show |
57 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.2503-1898_2503-188 others(16): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(6): Show |
41 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0133 others(38): Show |
44 | HG00099.hp1 HG00738.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.2503-1899_2503-188 others(17): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(7): Show |
69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
92 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.2503-1900_2503-188 others(18): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(8): Show |
43 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0023 others(40): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.2503-1901_2503-188 others(19): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(9): Show |
20 | a0001c0001t0001g0143 a0001c0001t0001g0166 a0001c0001t0001g0167 others(17): Show |
21 | HG00597.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.2503-1902_2503-188 others(20): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(10): Show |
25 | a0001c0001t0001g0191 a0001c0001t0002g0037 a0001c0001t0003g0029 others(22): Show |
28 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.2503-1903_2503-188 others(21): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(11): Show |
14 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0202 others(11): Show |
18 | HG00621.hp2 HG00639.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.2503-1904_2503-188 others(22): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(12): Show |
12 | a0001c0001t0003g0027 a0001c0001t0003g0194 a0001c0001t0003g0206 others(9): Show |
13 | HG00408.hp2 HG01261.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.2503-1905_2503-188 others(23): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0003g0205 a0001c0001t0003g0217 |
2 | HG03831.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2503-1887_2503-188 others(24): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511456 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0003g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2503-1887_2503-188 others(25): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511456 | ||||||
| chr17:43511479 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2503-1883A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43511479 | |||||||
| chr17:43511822 | T | C | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2503-1540T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43511822 | |||||||
| chr17:43511823 | G | T | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2503-1539G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43511823 | |||||||
| chr17:43511851 | C | CA | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0136 others(15): Show |
20 | HG01069.hp2 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.2503-1490dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511851 | ||||||
| chr17:43511851 | CA | C | 14 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
16 | HG01074.hp1 HG01891.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.2503-1490delA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511851 | ||||||
| chr17:43511851 | CAA | C | 28 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0019 others(25): Show |
32 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.2503-1491_2503-149 others(6): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511851 | ||||||
| chr17:43511851 | CAAA | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(55): Show |
72 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.2503-1492_2503-149 others(7): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43511851 | ||||||
| chr17:43511995 | A | G | 204 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(201): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2503-1367A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43511995 | |||||||
| chr17:43512111 | G | A | 75 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(72): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2503-1251G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512111 | |||||||
| chr17:43512373 | T | G | 17 | a0001c0001t0003g0012 a0001c0001t0003g0029 a0001c0001t0003g0121 others(14): Show |
18 | HG01884.hp2 HG02280.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.2503-989T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512373 | |||||||
| chr17:43512382 | A | G | 216 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0129 others(213): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.2503-980A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512382 | |||||||
| chr17:43512386 | C | CA | 85 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(82): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2503-960dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr17 | 43512386 | ||||||
| chr17:43512502 | G | A | 1 | a0001c0006t0007g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2503-860G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512502 | |||||||
| chr17:43512771 | AGTGACAG others(14): Show |
A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2503-590_2503-570d others(23): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512771 | |||||||
| chr17:43512917 | C | A | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2503-445C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512917 | |||||||
| chr17:43512923 | A | G | 1 | a0001c0001t0012g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2503-439A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43512923 | |||||||
| chr17:43513047 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503-315A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 16/22 | chr17 | 43513047 | |||||||
| chr17:43513560 | C | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2643+58C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43513560 | |||||||
| chr17:43513709 | C | CT | 25 | a0001c0001t0001g0133 a0001c0001t0001g0147 a0001c0001t0001g0167 others(22): Show |
27 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.2643+228dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43513709 | ||||||
| chr17:43513709 | C | CTT | 6 | a0001c0001t0002g0065 a0001c0001t0002g0079 a0001c0001t0002g0082 others(3): Show |
6 | HG02055.hp1 HG03516.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2643+227_2643+228d others(4): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43513709 | ||||||
| chr17:43513709 | C | CTTT | 66 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0015 others(63): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.2643+226_2643+228d others(5): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43513709 | ||||||
| chr17:43513709 | C | CTTTT | 9 | a0001c0001t0002g0014 a0001c0001t0002g0048 a0001c0001t0002g0059 others(6): Show |
10 | HG01928.hp2 HG02293.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.2643+225_2643+228d others(6): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43513709 | ||||||
| chr17:43513709 | C | CTTTTT | 8 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
10 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2643+224_2643+228d others(7): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43513709 | ||||||
| chr17:43513709 | CT | C | 11 | a0001c0001t0001g0123 a0001c0001t0001g0138 a0001c0001t0001g0151 others(8): Show |
11 | HG00408.hp1 HG01074.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2643+228delT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43513709 | ||||||
| chr17:43513753 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0140 a0001c0001t0001g0148 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.2643+251G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43513753 | |||||||
| chr17:43513775 | G | A | 3 | a0001c0001t0010g0265 a0001c0001t0010g0266 a0001c0001t0016g0267 |
3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2643+273G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43513775 | |||||||
| chr17:43513809 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2643+307G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43513809 | |||||||
| chr17:43513938 | C | T | 6 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(3): Show |
6 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2643+436C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43513938 | |||||||
| chr17:43514009 | G | A | 86 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2643+507G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514009 | |||||||
| chr17:43514056 | G | A | 6 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(3): Show |
6 | HG03041.hp2 HG03130.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2643+554G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514056 | |||||||
| chr17:43514149 | C | A | 7 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0271 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2643+647C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514149 | |||||||
| chr17:43514187 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2643+685T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514187 | |||||||
| chr17:43514187 | T | TA | 95 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0011 others(92): Show |
110 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.2643+693dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 43514187 | ||||||
| chr17:43514188 | A | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(72): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2643+686A>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514188 | |||||||
| chr17:43514307 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2643+805T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514307 | |||||||
| chr17:43514765 | T | C | 1 | a0001c0001t0008g0256 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2643+1263T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514765 | |||||||
| chr17:43514817 | A | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG02027.hp1 HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2643+1315A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43514817 | |||||||
| chr17:43515081 | A | G | 4 | a0001c0001t0008g0257 a0001c0001t0008g0258 a0001c0001t0017g0254 others(1): Show |
4 | HG03130.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2643+1579A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515081 | |||||||
| chr17:43515122 | T | G | 1 | a0001c0001t0003g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2643+1620T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515122 | |||||||
| chr17:43515142 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2643+1640G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515142 | |||||||
| chr17:43515151 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2643+1649A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515151 | |||||||
| chr17:43515156 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2643+1654G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515156 | |||||||
| chr17:43515244 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2643+1742A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515244 | |||||||
| chr17:43515341 | G | A | 13 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(10): Show |
15 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2644-1826G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515341 | |||||||
| chr17:43515443 | T | C | 1 | a0001c0001t0008g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2644-1724T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515443 | |||||||
| chr17:43515502 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1665C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515502 | |||||||
| chr17:43515507 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1660A>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515507 | |||||||
| chr17:43515508 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1659G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515508 | |||||||
| chr17:43515509 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1658T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515509 | |||||||
| chr17:43515513 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1654C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515513 | |||||||
| chr17:43515545 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1622G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515545 | |||||||
| chr17:43515546 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1621C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515546 | |||||||
| chr17:43515551 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1616T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515551 | |||||||
| chr17:43515553 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1614G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515553 | |||||||
| chr17:43515554 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1613C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515554 | |||||||
| chr17:43515557 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1610T>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515557 | |||||||
| chr17:43515565 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1602T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515565 | |||||||
| chr17:43515567 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1600T>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515567 | |||||||
| chr17:43515575 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1592A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515575 | |||||||
| chr17:43515584 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2644-1583A>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515584 | |||||||
| chr17:43515596 | C | G | 2 | a0001c0001t0008g0255 a0001c0001t0008g0256 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2644-1571C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515596 | |||||||
| chr17:43515759 | G | T | 1 | a0001c0001t0005g0220 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2644-1408G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515759 | |||||||
| chr17:43515762 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2644-1405A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515762 | |||||||
| chr17:43515851 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2644-1316T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515851 | |||||||
| chr17:43515963 | G | A | 3 | a0001c0001t0008g0257 a0001c0001t0008g0258 a0001c0001t0017g0254 |
3 | HG03130.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2644-1204G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43515963 | |||||||
| chr17:43516192 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2644-975C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516192 | |||||||
| chr17:43516237 | A | G | 1 | a0001c0001t0019g0252 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2644-930A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516237 | |||||||
| chr17:43516320 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0069 |
3 | HG02647.hp1 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2644-847T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516320 | |||||||
| chr17:43516389 | G | A | 9 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0107 others(6): Show |
11 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2644-778G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516389 | |||||||
| chr17:43516587 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0089 |
2 | NA18943.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2644-580T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516587 | |||||||
| chr17:43516589 | C | T | 7 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0271 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2644-578C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516589 | |||||||
| chr17:43516654 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2644-513G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516654 | |||||||
| chr17:43516714 | G | A | 1 | a0001c0001t0003g0116 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2644-453G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516714 | |||||||
| chr17:43516734 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2644-433C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516734 | |||||||
| chr17:43516737 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2644-430C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516737 | |||||||
| chr17:43516800 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2644-367G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516800 | |||||||
| chr17:43516859 | C | G | 2 | a0001c0001t0010g0265 a0001c0001t0010g0266 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2644-308C>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 17/22 | chr17 | 43516859 | |||||||
| chr17:43517631 | A | G | 3 | a0001c0001t0002g0037 a0001c0001t0002g0075 a0001c0001t0002g0101 |
3 | HG02486.hp2 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2799+309A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43517631 | |||||||
| chr17:43517648 | C | T | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2799+326C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43517648 | |||||||
| chr17:43518154 | A | G | 2 | a0001c0001t0001g0133 a0004c0007t0001g0132 |
2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2799+832A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43518154 | |||||||
| chr17:43518330 | C | T | 2 | a0001c0001t0001g0133 a0004c0007t0001g0132 |
2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2799+1008C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43518330 | |||||||
| chr17:43518573 | ATAT | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(89): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.2799+1268_2799+127 others(7): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 43518573 | ||||||
| chr17:43518604 | A | G | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2799+1282A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43518604 | |||||||
| chr17:43518863 | A | G | 2 | a0001c0001t0008g0255 a0001c0001t0008g0256 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2800-1267A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43518863 | |||||||
| chr17:43518881 | A | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0149 a0001c0001t0001g0159 others(2): Show |
7 | HG00544.hp1 HG00621.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800-1249A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43518881 | |||||||
| chr17:43519246 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2800-884G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519246 | |||||||
| chr17:43519310 | A | G | 8 | a0001c0001t0008g0255 a0001c0001t0008g0256 a0001c0001t0008g0257 others(5): Show |
8 | HG02895.hp1 HG03041.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2800-820A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519310 | |||||||
| chr17:43519311 | G | A | 1 | a0001c0001t0017g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2800-819G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519311 | |||||||
| chr17:43519522 | G | GT | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2800-597dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 43519522 | ||||||
| chr17:43519579 | G | A | 2 | a0001c0001t0003g0219 a0001c0001t0005g0220 |
2 | HG00642.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2800-551G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519579 | |||||||
| chr17:43519727 | G | C | 1 | a0001c0001t0002g0092 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2800-403G>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519727 | |||||||
| chr17:43519744 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2800-386C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519744 | |||||||
| chr17:43519849 | A | G | 204 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(201): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2800-281A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519849 | |||||||
| chr17:43519856 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2800-274G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519856 | |||||||
| chr17:43519891 | A | C | 78 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2800-239A>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519891 | |||||||
| chr17:43519935 | T | C | 2 | a0001c0001t0008g0262 a0001c0001t0012g0104 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2800-195T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 18/22 | chr17 | 43519935 | |||||||
| chr17:43520359 | G | A | 3 | a0001c0001t0010g0265 a0001c0001t0010g0266 a0001c0001t0016g0267 |
3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2937+92G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 19/22 | chr17 | 43520359 | |||||||
| chr17:43520910 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3066+31G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/22 | chr17 | 43520910 | |||||||
| chr17:43520964 | C | CT | 90 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0167 others(87): Show |
105 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.3066+109dupT | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 43520964 | ||||||
| chr17:43520964 | C | CTT | 22 | a0001c0001t0002g0007 a0001c0001t0002g0106 a0001c0001t0002g0108 others(19): Show |
25 | HG01069.hp2 HG01884.hp2 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.3066+108_3066+109d others(4): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 43520964 | ||||||
| chr17:43520964 | CTTTTTT | C | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3066+104_3066+109d others(8): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 43520964 | ||||||
| chr17:43520999 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3066+120C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/22 | chr17 | 43520999 | |||||||
| chr17:43521043 | A | G | 1 | a0001c0001t0003g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3066+164A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 20/22 | chr17 | 43521043 | |||||||
| chr17:43521572 | T | C | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(105): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
splice_region_variant&intron_variant | LOW | c.3263+7T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 21/22 | chr17 | 43521572 | |||||||
| chr17:43521573 | G | A | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.3263+8G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 21/22 | chr17 | 43521573 | |||||||
| chr17:43521956 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3264-91G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 21/22 | chr17 | 43521956 | |||||||
| chr17:43522015 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.3264-32G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 21/22 | chr17 | 43522015 | |||||||
| chr17:43522035 | C | T | 10 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0268 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3264-12C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 21/22 | chr17 | 43522035 | |||||||
| chr17:43522322 | G | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.3443+96G>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43522322 | |||||||
| chr17:43522414 | T | C | 1 | a0001c0001t0009g0084 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3443+188T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43522414 | |||||||
| chr17:43522538 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0272 others(3): Show |
8 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3443+312C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43522538 | |||||||
| chr17:43522703 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.3443+477A>G | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43522703 | |||||||
| chr17:43522747 | C | CA | 48 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0134 others(45): Show |
51 | HG00621.hp1 HG00639.hp1 HG01261.hp2 others(48): Show |
intron_variant | MODIFIER | c.3443+542dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 43522747 | ||||||
| chr17:43522747 | C | CAA | 9 | a0001c0001t0004g0031 a0001c0001t0004g0270 a0001c0001t0004g0271 others(6): Show |
10 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.3443+541_3443+542d others(4): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 43522747 | ||||||
| chr17:43522747 | C | CAAA | 6 | a0001c0001t0004g0030 a0001c0001t0004g0268 a0001c0001t0010g0265 others(3): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3443+540_3443+542d others(5): Show |
DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 43522747 | ||||||
| chr17:43522769 | C | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.3443+543C>A | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43522769 | |||||||
| chr17:43522839 | G | T | 1 | a0001c0001t0003g0243 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3443+613G>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43522839 | |||||||
| chr17:43523062 | C | CA | 81 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(78): Show |
99 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.3444-549dupA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 43523062 | ||||||
| chr17:43523062 | CA | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.3444-549delA | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 43523062 | ||||||
| chr17:43523114 | A | T | 1 | a0001c0001t0002g0078 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3444-514A>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43523114 | |||||||
| chr17:43523432 | T | C | 87 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0013 others(84): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.3444-196T>C | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43523432 | |||||||
| chr17:43523618 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0096 |
3 | HG01943.hp1 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3444-10C>T | DHX8 | ENSG00000067596.12 | transcript | ENST00000262415.8 | protein_coding | 22/22 | chr17 | 43523618 |