Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 284004 |
| ensemblid | ENSG00000169660.17 |
| hgncid | 26307 |
| symbol | HEXD |
| name | hexosaminidase D |
| refseq_nuc | NM_001330542.2 |
| refseq_prot | NP_001317471.1 |
| ensembl_nuc | ENST00000327949.15 |
| ensembl_prot | ENSP00000332634.9 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 82418347 |
| end | 82442645 |
| strand | + |
| ver | v1.2 |
| region | chr17:82418347-82442645 |
| region5000 | chr17:82413347-82447645 |
| regionname0 | HEXD_chr17_82418347_82442645 |
| regionname5000 | HEXD_chr17_82413347_82447645 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 486 | 264 | 46 | 39 | 156 | 5 | 18 | 118 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0002 | 1/1 | 486 | 126 | 46 | 29 | 14 | 11 | 24 | 12 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0003 | 0/0 | 486 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0004 | 0/0 | 486 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0005 | 0/0 | 486 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0006 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0007 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0008 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| a0009 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | MSGST others(481): Show |
chr17 | 82413347 | 82447645 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1458 | 178 | 41 | 21 | 103 | 5 | 8 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0003 | 0/0 | 1458 | 75 | 1 | 18 | 46 | 0 | 10 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0006 | 0/0 | 1458 | 4 | 0 | 0 | 4 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0007 | 0/0 | 1458 | 3 | 3 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0011 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0013 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0014 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0001c0015 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0002c0002 | 1/1 | 1458 | 93 | 22 | 25 | 10 | 11 | 23 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0002c0004 | 0/0 | 1458 | 27 | 21 | 2 | 3 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0002c0005 | 0/0 | 1458 | 5 | 3 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0002c0010 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0003c0008 | 0/0 | 1458 | 3 | 2 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0004c0009 | 0/0 | 1458 | 2 | 0 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0005c0012 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0006c0019 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0007c0016 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0008c0018 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 | ||
| a0009c0017 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | ATGTC others(1453): Show |
chr17 | 82413347 | 82447645 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2167 | 172 | 37 | 21 | 101 | 5 | 8 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0001t0002 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0001t0003 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGCCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0001t0004 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0001t0005 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0001t0006 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0001t0007 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCT others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0003t0001 | 0/0 | 2167 | 75 | 1 | 18 | 46 | 0 | 10 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0006t0001 | 0/0 | 2167 | 4 | 0 | 0 | 4 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0007t0001 | 0/0 | 2167 | 3 | 3 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0011t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0013t0002 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0014t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0001c0015t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0002c0002t0001 | 1/1 | 2167 | 93 | 22 | 25 | 10 | 11 | 23 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0002c0004t0001 | 0/0 | 2167 | 27 | 21 | 2 | 3 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0002c0005t0001 | 0/0 | 2167 | 5 | 3 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0002c0010t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0003c0008t0001 | 0/0 | 2167 | 3 | 2 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0004c0009t0001 | 0/0 | 2167 | 2 | 0 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0005c0012t0001 | 0/0 | 2167 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0006c0019t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0007c0016t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0008c0018t0001 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| a0009c0017t0001 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | AGTCC others(2162): Show |
chr17 | 82413347 | 82447645 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0001 | 0/0 | 22 | 0 | 7 | 15 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0006t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0007t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0007t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0011t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0013t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0014t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0001c0015t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0002 | 0/0 | 17 | 3 | 9 | 0 | 4 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0006 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0005t0001g0003 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0002c0010t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0003c0008t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0003c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0004c0009t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0005c0012t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0006c0019t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0007c0016t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0008c0018t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| a0009c0017t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0085 | EUR | GBR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0074 | EUR | FIN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00544 | hp1 | a0001 | c0006 | t0001 | g0259 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00733 | hp2 | a0002 | c0004 | t0001 | g0247 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0117 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01099 | hp1 | a0004 | c0009 | t0001 | g0012 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01167 | hp2 | a0002 | c0005 | t0001 | g0003 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01243 | hp2 | a0003 | c0008 | t0001 | g0023 | AMR | PUR | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01261 | hp1 | a0002 | c0005 | t0001 | g0003 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01928 | hp2 | a0004 | c0009 | t0001 | g0012 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01952 | hp2 | a0005 | c0012 | t0001 | g0008 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0147 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0143 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02040 | hp1 | a0006 | c0019 | t0001 | g0145 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0054 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02071 | hp1 | a0007 | c0016 | t0001 | g0271 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0041 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CDX | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02258 | hp2 | a0002 | c0004 | t0001 | g0039 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02280 | hp2 | a0008 | c0018 | t0001 | g0092 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02300 | hp1 | a0002 | c0004 | t0001 | g0231 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02622 | hp1 | a0001 | c0007 | t0001 | g0024 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0043 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0131 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0102 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02717 | hp2 | a0003 | c0008 | t0001 | g0023 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0044 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02735 | hp1 | a0002 | c0004 | t0001 | g0045 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0159 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0215 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02886 | hp2 | a0002 | c0004 | t0001 | g0200 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02895 | hp1 | a0002 | c0004 | t0001 | g0042 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0024 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02896 | hp1 | a0002 | c0005 | t0001 | g0003 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02896 | hp2 | a0001 | c0007 | t0001 | g0162 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0016 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02965 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0210 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03041 | hp2 | a0002 | c0004 | t0001 | g0208 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03130 | hp1 | a0001 | c0013 | t0002 | g0033 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03195 | hp1 | a0009 | c0017 | t0001 | g0003 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03225 | hp2 | a0002 | c0004 | t0001 | g0058 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0119 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0124 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0053 | AFR | ESN | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0071 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | BEB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0077 | SAS | BEB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | BEB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | BEB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0099 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0158 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0133 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0075 | SAS | STU | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | YRI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18522 | hp2 | a0003 | c0008 | t0001 | g0148 | AFR | YRI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18612 | hp1 | a0001 | c0006 | t0001 | g0248 | EAS | CHB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18747 | hp2 | a0001 | c0015 | t0001 | g0299 | EAS | CHB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18906 | hp1 | a0002 | c0004 | t0001 | g0205 | AFR | YRI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0125 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18983 | hp1 | a0001 | c0006 | t0001 | g0260 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18993 | hp1 | a0001 | c0014 | t0001 | g0264 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19002 | hp1 | a0002 | c0010 | t0001 | g0224 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19012 | hp2 | a0001 | c0006 | t0001 | g0294 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | LWK | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19030 | hp2 | a0002 | c0005 | t0001 | g0003 | AFR | LWK | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19058 | hp1 | a0002 | c0004 | t0001 | g0223 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19084 | hp2 | a0002 | c0004 | t0001 | g0291 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19085 | hp1 | a0001 | c0011 | t0001 | g0296 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19089 | hp1 | a0002 | c0004 | t0001 | g0225 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA19240 | hp2 | a0002 | c0005 | t0001 | g0003 | AFR | YRI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ASW | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20129 | hp2 | a0002 | c0004 | t0001 | g0016 | AFR | ASW | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0106 | EUR | TSI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | GIH | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02109 | hp1 | a0002 | c0004 | t0001 | g0209 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0214 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02559 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | USA | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| HG06807 | hp2 | a0002 | c0004 | t0001 | g0206 | AFR | USA | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | USA | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | LWK | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0088 | REF | REF | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0118 | REF | REF | HEXD_chr17_82413347_82447645 | HEXD | chr17 | 82413347 | 82447645 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82424496 | G | A | 1 | a0009 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.187G>A | p.Ala63Thr | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/13 | 632/2167 | 187/1461 | 63/486 | chr17 | 82424496 | |||
| chr17:82433757 | G | A | 1 | a0008 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.382G>A | p.Ala128Thr | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/13 | 827/2167 | 382/1461 | 128/486 | chr17 | 82433757 | |||
| chr17:82433808 | A | G | 5 | a0001 a0004 a0005 others(2): Show |
269 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(266): Show |
missense_variant | MODERATE | c.433A>G | p.Ile145Val | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/13 | 878/2167 | 433/1461 | 145/486 | chr17 | 82433808 | |||
| chr17:82435776 | C | T | 1 | a0004 | 2 | HG01099.hp1 HG01928.hp2 |
missense_variant | MODERATE | c.535C>T | p.Arg179Trp | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/13 | 980/2167 | 535/1461 | 179/486 | chr17 | 82435776 | |||
| chr17:82435780 | C | T | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.539C>T | p.Ala180Val | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/13 | 984/2167 | 539/1461 | 180/486 | chr17 | 82435780 | |||
| chr17:82435804 | G | A | 1 | a0003 | 3 | HG01243.hp2 HG02717.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.563G>A | p.Arg188Gln | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/13 | 1008/2167 | 563/1461 | 188/486 | chr17 | 82435804 | |||
| chr17:82441879 | G | A | 1 | a0006 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1243G>A | p.Ala415Thr | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 12/13 | 1688/2167 | 1243/1461 | 415/486 | chr17 | 82441879 | |||
| chr17:82442338 | C | G | 1 | a0005 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.1415C>G | p.Pro472Arg | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 13/13 | 1860/2167 | 1415/1461 | 472/486 | chr17 | 82442338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82419814 | T | G | 12 | a0001c0001 a0001c0006 a0001c0007 others(9): Show |
221 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
synonymous_variant | LOW | c.15T>G | p.Thr5Thr | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/13 | 460/2167 | 15/1461 | 5/486 | chr17 | 82419814 | |||
| chr17:82435793 | C | T | 2 | a0002c0005 a0009c0017 |
6 | HG01167.hp2 HG01261.hp1 HG02896.hp1 others(3): Show |
synonymous_variant | LOW | c.552C>T | p.Gly184Gly | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/13 | 997/2167 | 552/1461 | 184/486 | chr17 | 82435793 | |||
| chr17:82435805 | G | T | 1 | a0001c0015 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.564G>T | p.Arg188Arg | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/13 | 1009/2167 | 564/1461 | 188/486 | chr17 | 82435805 | |||
| chr17:82436716 | C | T | 1 | a0001c0014 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.681C>T | p.Ala227Ala | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/13 | 1126/2167 | 681/1461 | 227/486 | chr17 | 82436716 | |||
| chr17:82436731 | C | T | 1 | a0002c0010 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.696C>T | p.His232His | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/13 | 1141/2167 | 696/1461 | 232/486 | chr17 | 82436731 | |||
| chr17:82437217 | A | G | 1 | a0001c0006 | 4 | HG00544.hp1 NA18612.hp1 NA18983.hp1 others(1): Show |
synonymous_variant | LOW | c.753A>G | p.Ala251Ala | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/13 | 1198/2167 | 753/1461 | 251/486 | chr17 | 82437217 | |||
| chr17:82439667 | C | T | 1 | a0001c0013 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.936C>T | p.Pro312Pro | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/13 | 1381/2167 | 936/1461 | 312/486 | chr17 | 82439667 | |||
| chr17:82441180 | C | T | 1 | a0001c0007 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.1077C>T | p.Ser359Ser | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/13 | 1522/2167 | 1077/1461 | 359/486 | chr17 | 82441180 | |||
| chr17:82442243 | G | A | 1 | a0001c0011 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1320G>A | p.Pro440Pro | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 13/13 | 1765/2167 | 1320/1461 | 440/486 | chr17 | 82442243 | |||
| chr17:82442288 | G | A | 1 | a0001c0007 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.1365G>A | p.Leu455Leu | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 13/13 | 1810/2167 | 1365/1461 | 455/486 | chr17 | 82442288 | |||
| chr17:82442360 | C | A | 1 | a0001c0007 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.1437C>A | p.Gly479Gly | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 13/13 | 1882/2167 | 1437/1461 | 479/486 | chr17 | 82442360 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82418349 | T | C | 1 | a0001c0001t0003 | 1 | NA18980.hp1 | 5_prime_UTR_variant | MODIFIER | c.-443T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/13 | 1451 | chr17 | 82418349 | ||||||
| chr17:82418351 | C | T | 1 | a0001c0001t0007 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-441C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/13 | 1449 | chr17 | 82418351 | ||||||
| chr17:82418374 | G | A | 1 | a0001c0001t0004 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-418G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/13 | 1426 | chr17 | 82418374 | ||||||
| chr17:82418565 | G | A | 1 | a0001c0001t0005 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-227G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/13 | 1235 | chr17 | 82418565 | ||||||
| chr17:82418578 | G | A | 1 | a0001c0001t0005 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-214G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/13 | 1222 | chr17 | 82418578 | ||||||
| chr17:82418674 | C | T | 1 | a0001c0001t0006 | 1 | NA18990.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/13 | 1126 | chr17 | 82418674 | ||||||
| chr17:82419780 | A | C | 2 | a0001c0001t0002 a0001c0013t0002 |
2 | HG03130.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-20A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/13 | 20 | chr17 | 82419780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82418779 | C | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(148): Show |
171 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.-52+39C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82418779 | |||||||
| chr17:82418805 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-52+65C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82418805 | |||||||
| chr17:82418875 | G | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-52+135G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82418875 | |||||||
| chr17:82419105 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-52+365G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82419105 | |||||||
| chr17:82419183 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-52+443A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82419183 | |||||||
| chr17:82419238 | A | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-52+498A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82419238 | |||||||
| chr17:82419462 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-51-287G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82419462 | |||||||
| chr17:82419530 | T | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
221 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.-51-219T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82419530 | |||||||
| chr17:82419576 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51-173T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 1/12 | chr17 | 82419576 | |||||||
| chr17:82419887 | A | T | 1 | a0002c0002t0001g0161 | 1 | NA20905.hp1 | splice_region_variant&intron_variant | LOW | c.84+4A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82419887 | |||||||
| chr17:82420053 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.84+170C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420053 | |||||||
| chr17:82420066 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.84+183A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420066 | |||||||
| chr17:82420076 | C | T | 2 | a0001c0001t0001g0298 a0001c0015t0001g0299 |
2 | NA18747.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.84+193C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420076 | |||||||
| chr17:82420082 | G | A | 1 | a0001c0003t0001g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.84+199G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420082 | |||||||
| chr17:82420083 | GA | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.84+212delA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82420083 | ||||||
| chr17:82420427 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18950.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.84+544G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420427 | |||||||
| chr17:82420531 | T | C | 2 | a0001c0001t0002g0032 a0001c0013t0002g0033 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.84+648T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420531 | |||||||
| chr17:82420563 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.84+680G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420563 | |||||||
| chr17:82420646 | C | T | 1 | a0001c0001t0005g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+763C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420646 | |||||||
| chr17:82420756 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0004g0297 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.84+873C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420756 | |||||||
| chr17:82420984 | C | G | 1 | a0002c0002t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.84+1101C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82420984 | |||||||
| chr17:82421061 | G | C | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.84+1178G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421061 | |||||||
| chr17:82421062 | C | CCTCCAAA others(1): Show |
2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.84+1179_84+1180ins others(8): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421062 | |||||||
| chr17:82421063 | T | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.84+1180T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421063 | |||||||
| chr17:82421063 | T | C | 152 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(149): Show |
172 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.84+1180T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421063 | |||||||
| chr17:82421064 | A | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.84+1181A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421064 | |||||||
| chr17:82421065 | T | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.84+1182T>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421065 | |||||||
| chr17:82421081 | A | C | 1 | a0001c0003t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.84+1198A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421081 | |||||||
| chr17:82421107 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.84+1224T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421107 | |||||||
| chr17:82421182 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
17 | HG01081.hp2 HG01257.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.84+1299G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421182 | |||||||
| chr17:82421366 | C | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.84+1483C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421366 | |||||||
| chr17:82421443 | C | G | 2 | a0001c0001t0001g0295 a0001c0011t0001g0296 |
2 | NA18995.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.84+1560C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421443 | |||||||
| chr17:82421456 | T | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(152): Show |
175 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.84+1573T>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421456 | |||||||
| chr17:82421654 | C | T | 1 | a0002c0002t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.84+1771C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421654 | |||||||
| chr17:82421757 | C | T | 1 | a0002c0002t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.84+1874C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421757 | |||||||
| chr17:82421941 | C | G | 1 | a0001c0006t0001g0294 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.84+2058C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82421941 | |||||||
| chr17:82422036 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.84+2153C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422036 | |||||||
| chr17:82422037 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0005c0012t0001g0008 |
4 | HG01081.hp2 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+2154G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422037 | |||||||
| chr17:82422108 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.84+2225G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422108 | |||||||
| chr17:82422166 | C | CA | 7 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG00323.hp1 HG01433.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-2213dupA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82422166 | ||||||
| chr17:82422166 | CA | C | 10 | a0001c0001t0001g0168 a0001c0001t0001g0290 a0001c0001t0001g0292 others(7): Show |
11 | HG02074.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.85-2213delA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82422166 | ||||||
| chr17:82422306 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
17 | HG01081.hp2 HG01257.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.85-2088G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422306 | |||||||
| chr17:82422309 | A | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.85-2085A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422309 | |||||||
| chr17:82422363 | G | A | 1 | a0002c0002t0001g0009 | 3 | HG01346.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.85-2031G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422363 | |||||||
| chr17:82422364 | G | T | 1 | a0001c0013t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.85-2030G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422364 | |||||||
| chr17:82422365 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.85-2029C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422365 | |||||||
| chr17:82422405 | G | C | 1 | a0002c0002t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.85-1989G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422405 | |||||||
| chr17:82422495 | T | TA | 197 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
221 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.85-1887dupA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82422495 | ||||||
| chr17:82422638 | A | G | 1 | a0001c0003t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.85-1756A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422638 | |||||||
| chr17:82422855 | G | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02273.hp2 HG02735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-1539G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422855 | |||||||
| chr17:82422934 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.85-1460G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422934 | |||||||
| chr17:82422969 | A | C | 1 | a0001c0001t0005g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85-1425A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82422969 | |||||||
| chr17:82423012 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0176 |
3 | HG02630.hp2 HG02809.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.85-1382G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423012 | |||||||
| chr17:82423057 | C | CA | 36 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0025 others(33): Show |
46 | HG00558.hp2 HG00597.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.85-1326dupA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82423057 | ||||||
| chr17:82423091 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.85-1303T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423091 | |||||||
| chr17:82423144 | A | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.85-1250A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423144 | |||||||
| chr17:82423214 | G | T | 1 | a0001c0001t0005g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85-1180G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423214 | |||||||
| chr17:82423224 | G | A | 4 | a0001c0001t0005g0062 a0001c0003t0001g0018 a0002c0002t0001g0078 others(1): Show |
5 | HG01106.hp1 NA18906.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-1170G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423224 | |||||||
| chr17:82423235 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.85-1159T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423235 | |||||||
| chr17:82423481 | C | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
106 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.85-913C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423481 | |||||||
| chr17:82423642 | G | A | 1 | a0001c0003t0001g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.85-752G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423642 | |||||||
| chr17:82423682 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(5): Show |
8 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-712G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423682 | |||||||
| chr17:82423727 | C | T | 3 | a0001c0001t0002g0032 a0001c0001t0005g0062 a0001c0013t0002g0033 |
3 | HG03130.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.85-667C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423727 | |||||||
| chr17:82423728 | G | A | 2 | a0001c0001t0002g0032 a0001c0013t0002g0033 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.85-666G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423728 | |||||||
| chr17:82423791 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-603C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423791 | |||||||
| chr17:82423797 | A | C | 4 | a0002c0002t0001g0003 a0002c0002t0001g0153 a0002c0005t0001g0003 others(1): Show |
15 | HG01167.hp2 HG01168.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.85-597A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423797 | |||||||
| chr17:82423812 | C | CA | 35 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(32): Show |
38 | HG00140.hp1 HG01081.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.85-566dupA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82423812 | ||||||
| chr17:82423827 | AAGAG | A | 6 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0002c0002t0001g0084 others(3): Show |
6 | HG00099.hp2 HG01361.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-563_85-560delGA others(2): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 82423827 | ||||||
| chr17:82423828 | AG | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-565delG | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423828 | |||||||
| chr17:82423851 | G | A | 1 | a0002c0002t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.85-543G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423851 | |||||||
| chr17:82423873 | C | T | 1 | a0002c0002t0001g0152 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.85-521C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423873 | |||||||
| chr17:82423976 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.85-418C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82423976 | |||||||
| chr17:82424065 | C | T | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG01099.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.85-329C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82424065 | |||||||
| chr17:82424150 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.85-244G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82424150 | |||||||
| chr17:82424151 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0006g0285 |
2 | HG00673.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.85-243C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82424151 | |||||||
| chr17:82424212 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85-182C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82424212 | |||||||
| chr17:82424286 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.85-108C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82424286 | |||||||
| chr17:82424296 | C | T | 9 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(6): Show |
11 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.85-98C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 2/12 | chr17 | 82424296 | |||||||
| chr17:82424532 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0065 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.194+29C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424532 | |||||||
| chr17:82424631 | A | G | 2 | a0003c0008t0001g0023 a0003c0008t0001g0148 |
3 | HG01243.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.194+128A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424631 | |||||||
| chr17:82424747 | G | A | 1 | a0002c0004t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.194+244G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424747 | |||||||
| chr17:82424755 | C | T | 9 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(6): Show |
11 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.194+252C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424755 | |||||||
| chr17:82424775 | T | C | 2 | a0001c0001t0002g0032 a0001c0013t0002g0033 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.194+272T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424775 | |||||||
| chr17:82424788 | C | A | 1 | a0002c0002t0001g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.194+285C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424788 | |||||||
| chr17:82424825 | CAGAAGGT others(3): Show |
C | 1 | a0002c0004t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.194+349_194+358del others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82424825 | ||||||
| chr17:82424845 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.194+342G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82424845 | |||||||
| chr17:82424921 | C | CTAGAGAA others(38): Show |
1 | a0001c0001t0001g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.194+429_194+473dup others(45): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82424921 | ||||||
| chr17:82424923 | AGAGAAGG others(3): Show |
A | 1 | a0001c0001t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.194+443_194+452del others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82424923 | ||||||
| chr17:82424997 | A | AAGGCCGG others(13): Show |
1 | a0001c0001t0001g0222 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.194+499_194+518dup others(20): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82424997 | ||||||
| chr17:82425032 | T | TGGAGGAG others(13): Show |
1 | a0002c0004t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.194+530_194+549dup others(20): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82425032 | ||||||
| chr17:82425053 | A | G | 233 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
291 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.194+550A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425053 | |||||||
| chr17:82425128 | A | AGAGAAGG others(3): Show |
133 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(130): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.194+639_194+648dup others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82425128 | ||||||
| chr17:82425138 | G | GGAGAAGG others(13): Show |
1 | a0001c0003t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.194+655_194+674dup others(20): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82425138 | ||||||
| chr17:82425142 | A | AAGGCTGG others(3): Show |
1 | a0001c0001t0002g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194+645_194+654dup others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82425142 | ||||||
| chr17:82425162 | AAGGCTGG others(3): Show |
A | 1 | a0002c0002t0001g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.194+674_194+683del others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82425162 | ||||||
| chr17:82425192 | AAGGCTGG others(3): Show |
A | 2 | a0001c0003t0001g0147 a0002c0002t0001g0151 |
2 | HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.194+707_194+716del others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82425192 | ||||||
| chr17:82425542 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.194+1039A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425542 | |||||||
| chr17:82425610 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194+1107A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425610 | |||||||
| chr17:82425616 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194+1113A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425616 | |||||||
| chr17:82425836 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.194+1333G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425836 | |||||||
| chr17:82425878 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(9): Show |
13 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+1375T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425878 | |||||||
| chr17:82425968 | G | A | 233 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
291 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.194+1465G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82425968 | |||||||
| chr17:82426015 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194+1512G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426015 | |||||||
| chr17:82426037 | GT | G | 231 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
289 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.194+1541delT | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82426037 | ||||||
| chr17:82426055 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.194+1552C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426055 | |||||||
| chr17:82426068 | AAGAC | A | 9 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(6): Show |
11 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.194+1569_194+1572d others(6): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82426068 | ||||||
| chr17:82426072 | CAGAG | C | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.194+1578_194+1581d others(6): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82426072 | ||||||
| chr17:82426218 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.194+1715C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426218 | |||||||
| chr17:82426276 | A | G | 233 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
291 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.194+1773A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426276 | |||||||
| chr17:82426355 | T | C | 51 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(48): Show |
85 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.194+1852T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426355 | |||||||
| chr17:82426462 | A | G | 231 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
289 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.194+1959A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426462 | |||||||
| chr17:82426644 | C | G | 1 | a0002c0002t0001g0123 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.195-1914C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426644 | |||||||
| chr17:82426697 | A | G | 147 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
167 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.195-1861A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426697 | |||||||
| chr17:82426851 | G | A | 9 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(6): Show |
11 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-1707G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426851 | |||||||
| chr17:82426873 | C | T | 1 | a0001c0003t0001g0124 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.195-1685C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426873 | |||||||
| chr17:82426964 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.195-1594G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82426964 | |||||||
| chr17:82427100 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0038 others(61): Show |
101 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.195-1458C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427100 | |||||||
| chr17:82427135 | C | CA | 21 | a0001c0001t0001g0164 a0001c0001t0001g0180 a0001c0001t0001g0181 others(18): Show |
22 | HG00140.hp1 HG01433.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.195-1405dupA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 82427135 | ||||||
| chr17:82427392 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(245): Show |
311 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.195-1166T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427392 | |||||||
| chr17:82427417 | C | T | 4 | a0001c0001t0001g0230 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18961.hp1 NA19056.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-1141C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427417 | |||||||
| chr17:82427569 | G | A | 1 | a0002c0004t0001g0231 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.195-989G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427569 | |||||||
| chr17:82427744 | G | A | 229 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(226): Show |
286 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.195-814G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427744 | |||||||
| chr17:82427795 | C | T | 1 | a0002c0002t0001g0100 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.195-763C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427795 | |||||||
| chr17:82427830 | G | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0038 others(61): Show |
101 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.195-728G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427830 | |||||||
| chr17:82427889 | G | T | 234 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(231): Show |
292 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(289): Show |
intron_variant | MODIFIER | c.195-669G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427889 | |||||||
| chr17:82427900 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.195-658A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427900 | |||||||
| chr17:82427910 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.195-648G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427910 | |||||||
| chr17:82427917 | A | G | 234 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(231): Show |
292 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(289): Show |
intron_variant | MODIFIER | c.195-641A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82427917 | |||||||
| chr17:82428077 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.195-481C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428077 | |||||||
| chr17:82428126 | A | G | 2 | a0002c0002t0001g0098 a0002c0002t0001g0099 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.195-432A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428126 | |||||||
| chr17:82428147 | G | A | 10 | a0001c0001t0001g0038 a0002c0002t0001g0149 a0002c0004t0001g0015 others(7): Show |
12 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.195-411G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428147 | |||||||
| chr17:82428152 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.195-406T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428152 | |||||||
| chr17:82428205 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.195-353G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428205 | |||||||
| chr17:82428265 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG02615.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195-293G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428265 | |||||||
| chr17:82428335 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0003g0177 |
2 | NA18972.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.195-223G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428335 | |||||||
| chr17:82428400 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-158T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 3/12 | chr17 | 82428400 | |||||||
| chr17:82428743 | A | G | 1 | a0002c0002t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.282+98A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82428743 | |||||||
| chr17:82428787 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0005c0012t0001g0008 |
4 | HG01081.hp2 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+142C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82428787 | |||||||
| chr17:82428838 | C | T | 1 | a0001c0003t0001g0146 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.282+193C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82428838 | |||||||
| chr17:82429058 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.282+413G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429058 | |||||||
| chr17:82429080 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.282+435C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429080 | |||||||
| chr17:82429215 | G | A | 1 | a0001c0001t0006g0285 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.282+570G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429215 | |||||||
| chr17:82429274 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.282+629T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429274 | |||||||
| chr17:82429296 | T | TGCATCAA others(15): Show |
2 | a0001c0001t0002g0032 a0001c0013t0002g0033 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.282+656_282+677dup others(22): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82429296 | ||||||
| chr17:82429336 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.282+691G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429336 | |||||||
| chr17:82429385 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.282+740C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429385 | |||||||
| chr17:82429397 | T | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02055.hp1 HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+752T>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429397 | |||||||
| chr17:82429461 | G | A | 1 | a0002c0002t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.282+816G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429461 | |||||||
| chr17:82429481 | G | A | 1 | a0001c0001t0005g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+836G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429481 | |||||||
| chr17:82429514 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02055.hp1 HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+869C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429514 | |||||||
| chr17:82429521 | T | C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+876T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429521 | |||||||
| chr17:82429560 | G | C | 230 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(227): Show |
288 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.282+915G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429560 | |||||||
| chr17:82429739 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.282+1094G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429739 | |||||||
| chr17:82429780 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+1135C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429780 | |||||||
| chr17:82429857 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.282+1212G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82429857 | |||||||
| chr17:82430029 | C | G | 1 | a0001c0003t0001g0146 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.282+1384C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430029 | |||||||
| chr17:82430067 | C | T | 1 | a0001c0003t0001g0146 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.282+1422C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430067 | |||||||
| chr17:82430137 | G | A | 147 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
167 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.282+1492G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430137 | |||||||
| chr17:82430440 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0003t0001g0102 others(1): Show |
5 | HG01081.hp2 HG01257.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+1795G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430440 | |||||||
| chr17:82430652 | G | A | 38 | a0001c0001t0001g0277 a0001c0001t0001g0300 a0001c0003t0001g0001 others(35): Show |
72 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.282+2007G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430652 | |||||||
| chr17:82430751 | A | G | 1 | a0007c0016t0001g0271 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.282+2106A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430751 | |||||||
| chr17:82430861 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(5): Show |
8 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+2216A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430861 | |||||||
| chr17:82430927 | G | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0059 a0001c0001t0001g0060 others(15): Show |
19 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+2282G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82430927 | |||||||
| chr17:82431052 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+2407G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431052 | |||||||
| chr17:82431113 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+2468G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431113 | |||||||
| chr17:82431169 | GT | G | 234 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(231): Show |
292 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(289): Show |
intron_variant | MODIFIER | c.283-2481delT | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82431169 | ||||||
| chr17:82431430 | A | AT | 13 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0164 others(10): Show |
13 | HG00673.hp2 HG02055.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-2212dupT | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82431430 | ||||||
| chr17:82431430 | A | T | 1 | a0002c0002t0001g0121 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.283-2228A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431430 | |||||||
| chr17:82431430 | AT | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0233 others(4): Show |
7 | HG01069.hp2 HG02055.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-2212delT | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82431430 | ||||||
| chr17:82431517 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0003t0001g0102 others(1): Show |
5 | HG01081.hp2 HG01257.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-2141A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431517 | |||||||
| chr17:82431562 | C | T | 51 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(48): Show |
58 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.283-2096C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431562 | |||||||
| chr17:82431589 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-2069T>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431589 | |||||||
| chr17:82431602 | C | T | 1 | a0001c0003t0001g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283-2056C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431602 | |||||||
| chr17:82431663 | C | T | 2 | a0002c0004t0001g0225 a0002c0010t0001g0224 |
2 | NA19002.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.283-1995C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431663 | |||||||
| chr17:82431713 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.283-1945G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431713 | |||||||
| chr17:82431778 | G | A | 2 | a0002c0004t0001g0209 a0002c0004t0001g0210 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.283-1880G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431778 | |||||||
| chr17:82431833 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-1825A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82431833 | |||||||
| chr17:82432025 | C | A | 1 | a0002c0002t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.283-1633C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432025 | |||||||
| chr17:82432055 | G | C | 1 | a0002c0002t0001g0103 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.283-1603G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432055 | |||||||
| chr17:82432060 | A | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0059 a0001c0001t0001g0060 others(11): Show |
14 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.283-1598A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432060 | |||||||
| chr17:82432195 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283-1463G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432195 | |||||||
| chr17:82432380 | C | T | 16 | a0001c0001t0001g0031 a0001c0001t0001g0167 a0001c0001t0001g0168 others(13): Show |
17 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.283-1278C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432380 | |||||||
| chr17:82432404 | G | A | 3 | a0001c0001t0001g0008 a0001c0003t0001g0102 a0005c0012t0001g0008 |
4 | HG01081.hp2 HG01433.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1254G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432404 | |||||||
| chr17:82432544 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.283-1114A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432544 | |||||||
| chr17:82432615 | C | T | 1 | a0001c0003t0001g0018 | 2 | NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.283-1043C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432615 | |||||||
| chr17:82432635 | G | A | 146 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(143): Show |
166 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.283-1023G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432635 | |||||||
| chr17:82432689 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.283-969G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432689 | |||||||
| chr17:82432789 | T | C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0198 others(3): Show |
6 | HG01884.hp2 HG02451.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-869T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432789 | |||||||
| chr17:82432792 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.283-866A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432792 | |||||||
| chr17:82432802 | G | A | 1 | a0002c0004t0001g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.283-856G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432802 | |||||||
| chr17:82432830 | A | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-828A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432830 | |||||||
| chr17:82432834 | C | T | 207 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(204): Show |
261 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.283-824C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432834 | |||||||
| chr17:82432846 | A | G | 9 | a0001c0001t0001g0057 a0002c0004t0001g0058 a0002c0004t0001g0205 others(6): Show |
9 | HG02109.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-812A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432846 | |||||||
| chr17:82432859 | C | G | 1 | a0002c0004t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.283-799C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432859 | |||||||
| chr17:82432859 | C | T | 1 | a0001c0003t0001g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.283-799C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432859 | |||||||
| chr17:82432864 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283-794C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432864 | |||||||
| chr17:82432873 | C | T | 51 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0028 others(48): Show |
57 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.283-785C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432873 | |||||||
| chr17:82432874 | T | C | 3 | a0001c0001t0001g0277 a0001c0003t0001g0081 a0001c0003t0001g0147 |
3 | HG01978.hp1 NA19004.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.283-784T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432874 | |||||||
| chr17:82432879 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.283-779C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432879 | |||||||
| chr17:82432880 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283-778G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432880 | |||||||
| chr17:82432884 | A | G | 120 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0026 others(117): Show |
132 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.283-774A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432884 | |||||||
| chr17:82432887 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0298 others(3): Show |
8 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-771C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432887 | |||||||
| chr17:82432890 | C | T | 145 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(142): Show |
187 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.283-768C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432890 | |||||||
| chr17:82432891 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0241 others(4): Show |
9 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-767G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432891 | |||||||
| chr17:82432922 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.283-736C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432922 | |||||||
| chr17:82432923 | G | A | 300 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.283-735G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432923 | |||||||
| chr17:82432926 | C | T | 302 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.283-732C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432926 | |||||||
| chr17:82432939 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283-719G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82432939 | |||||||
| chr17:82433021 | A | G | 1 | a0001c0013t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283-637A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433021 | |||||||
| chr17:82433022 | T | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0013t0002g0033 |
3 | HG03130.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-636T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433022 | |||||||
| chr17:82433025 | C | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0055 |
3 | HG02630.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.283-633C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433025 | |||||||
| chr17:82433038 | A | C | 11 | a0001c0001t0001g0055 a0002c0002t0001g0149 a0002c0004t0001g0015 others(8): Show |
13 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-620A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433038 | |||||||
| chr17:82433045 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.283-613G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433045 | |||||||
| chr17:82433053 | A | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.283-605A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433053 | |||||||
| chr17:82433061 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.283-597A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433061 | |||||||
| chr17:82433076 | A | G | 2 | a0001c0001t0001g0240 a0001c0003t0001g0137 |
2 | HG02523.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.283-582A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433076 | |||||||
| chr17:82433077 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0240 a0001c0003t0001g0137 |
3 | HG02523.hp2 NA18959.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.283-581G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433077 | |||||||
| chr17:82433077 | G | GA | 18 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0047 others(15): Show |
20 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.283-566dupA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAA | 15 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0192 others(12): Show |
16 | HG00423.hp2 HG00673.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-568_283-566dup others(3): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAA | 10 | a0001c0001t0001g0163 a0001c0001t0001g0175 a0001c0001t0001g0216 others(7): Show |
10 | HG00544.hp1 HG00741.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-570_283-566dup others(5): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAA | 6 | a0001c0001t0001g0183 a0001c0001t0001g0204 a0001c0001t0001g0241 others(3): Show |
6 | HG00323.hp1 HG01358.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-571_283-566dup others(6): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.283-575_283-566dup others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(4): Show |
1 | a0002c0002t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.283-576_283-566dup others(11): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(5): Show |
2 | a0001c0001t0001g0292 a0002c0002t0001g0098 |
2 | HG02074.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.283-577_283-566dup others(12): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(7): Show |
1 | a0007c0016t0001g0271 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.283-579_283-566dup others(14): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(8): Show |
1 | a0008c0018t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.283-580_283-566dup others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(13): Show |
1 | a0002c0002t0001g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(20): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | G | GAAAAAAA others(16): Show |
1 | a0002c0004t0001g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(23): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433077 | GA | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0164 a0001c0003t0001g0117 others(5): Show |
9 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-566delA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433077 | ||||||
| chr17:82433079 | A | AG | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0203 |
3 | HG01074.hp1 HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283-579_283-578ins others(1): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433079 | |||||||
| chr17:82433080 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283-578A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433080 | |||||||
| chr17:82433089 | A | T | 1 | a0002c0002t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.283-569A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433089 | |||||||
| chr17:82433091 | A | AAAAAAAA others(15): Show |
1 | a0002c0002t0001g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(22): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(21): Show |
1 | a0002c0002t0001g0100 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(28): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(17): Show |
1 | a0002c0002t0001g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(24): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(12): Show |
1 | a0002c0004t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(11): Show |
1 | a0002c0002t0001g0010 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(18): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(13): Show |
1 | a0002c0002t0001g0010 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(20): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(15): Show |
1 | a0002c0002t0001g0010 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(22): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0188 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(32): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(17): Show |
1 | a0002c0002t0001g0006 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(24): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(14): Show |
1 | a0002c0002t0001g0006 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(21): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0287 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(14): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(9): Show |
1 | a0002c0002t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(16): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(8): Show |
1 | a0002c0002t0001g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0037 a0002c0002t0001g0154 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.283-566_283-565ins others(12): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(8): Show |
1 | a0002c0002t0001g0009 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(9): Show |
1 | a0002c0002t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(16): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(11): Show |
1 | a0003c0008t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(18): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0288 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(11): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(12): Show |
1 | a0002c0004t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0269 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(7): Show |
1 | a0002c0002t0001g0009 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.283-566_283-565ins others(14): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAA others(11): Show |
1 | a0002c0002t0001g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(18): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAAAT others(10): Show |
1 | a0002c0002t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0268 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(12): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAATA others(7): Show |
1 | a0002c0002t0001g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(14): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAAATA others(19): Show |
1 | a0002c0002t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(26): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAAAATAT others(6): Show |
1 | a0002c0002t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283-566_283-565ins others(13): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | AAATATAT others(4): Show |
1 | a0002c0002t0001g0021 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.283-566_283-565ins others(11): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433091 | ||||||
| chr17:82433091 | A | T | 6 | a0001c0003t0001g0020 a0001c0003t0001g0117 a0002c0002t0001g0002 others(3): Show |
6 | HG00099.hp2 HG00738.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-567A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433091 | |||||||
| chr17:82433092 | AT | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(81): Show |
110 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.283-565delT | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433092 | |||||||
| chr17:82433092 | ATATATAT others(8): Show |
A | 2 | a0002c0002t0001g0003 a0002c0005t0001g0003 |
2 | HG01261.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283-565_283-551del others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433092 | |||||||
| chr17:82433093 | T | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(150): Show |
183 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.283-565T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433093 | |||||||
| chr17:82433095 | T | A | 189 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(186): Show |
242 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.283-563T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433095 | |||||||
| chr17:82433097 | T | A | 156 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(153): Show |
206 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.283-561T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433097 | |||||||
| chr17:82433099 | T | A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(119): Show |
168 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.283-559T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433099 | |||||||
| chr17:82433101 | T | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(79): Show |
122 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.283-557T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433101 | |||||||
| chr17:82433103 | T | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(54): Show |
86 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.283-555T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433103 | |||||||
| chr17:82433104 | ATATATAT others(32): Show |
A | 2 | a0001c0001t0001g0036 a0001c0001t0005g0062 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.283-542_283-504del others(39): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433104 | ||||||
| chr17:82433105 | T | A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(29): Show |
44 | HG00423.hp1 HG00597.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.283-553T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433105 | |||||||
| chr17:82433106 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283-550_283-516del others(35): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433106 | ||||||
| chr17:82433106 | ATATATAT others(30): Show |
A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.283-540_283-504del others(37): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433106 | ||||||
| chr17:82433107 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(11): Show |
16 | HG02040.hp1 HG02074.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-551T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433107 | |||||||
| chr17:82433108 | ATATATAT others(28): Show |
A | 3 | a0001c0003t0001g0080 a0001c0003t0001g0102 a0005c0012t0001g0008 |
3 | HG01928.hp1 HG01952.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.283-538_283-504del others(35): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433108 | ||||||
| chr17:82433109 | T | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG02040.hp1 HG02273.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-549T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433109 | |||||||
| chr17:82433109 | TATATATA others(6): Show |
T | 1 | a0002c0002t0001g0121 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.283-548_283-536del others(13): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433109 | |||||||
| chr17:82433110 | ATATATAT others(26): Show |
A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0249 others(10): Show |
20 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-536_283-504del others(33): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433110 | ||||||
| chr17:82433111 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.283-547T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433111 | |||||||
| chr17:82433111 | TATATATA others(10): Show |
T | 1 | a0002c0005t0001g0003 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.283-546_283-530del others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433111 | |||||||
| chr17:82433112 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0286 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.283-544_283-516del others(29): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433112 | ||||||
| chr17:82433112 | ATATATAT others(24): Show |
A | 36 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0274 others(33): Show |
59 | HG00423.hp1 HG00597.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.283-534_283-504del others(31): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433112 | ||||||
| chr17:82433113 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.283-545T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433113 | |||||||
| chr17:82433113 | TATATATA others(8): Show |
T | 4 | a0002c0002t0001g0003 a0002c0002t0001g0153 a0002c0005t0001g0003 others(1): Show |
11 | HG01168.hp1 HG02647.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-544_283-530del others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433113 | |||||||
| chr17:82433114 | ATATATAT others(8): Show |
A | 1 | a0002c0002t0001g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.283-542_283-528del others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433114 | ||||||
| chr17:82433114 | ATATATAT others(22): Show |
A | 7 | a0001c0001t0001g0055 a0001c0003t0001g0001 a0001c0003t0001g0004 others(4): Show |
9 | HG02074.hp2 HG02300.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-532_283-504del others(29): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433114 | ||||||
| chr17:82433115 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.283-543T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433115 | |||||||
| chr17:82433116 | ATATATAT others(8): Show |
A | 1 | a0002c0002t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.283-540_283-526del others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433116 | ||||||
| chr17:82433116 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0007 | 3 | NA18963.hp1 NA18966.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.283-540_283-516del others(25): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433116 | ||||||
| chr17:82433116 | ATATATAT others(20): Show |
A | 1 | a0001c0003t0001g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.283-530_283-504del others(27): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433116 | ||||||
| chr17:82433120 | A | T | 1 | a0001c0003t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.283-538A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433120 | |||||||
| chr17:82433120 | ATATATAT others(4): Show |
A | 2 | a0002c0002t0001g0078 a0002c0002t0001g0095 |
2 | HG01106.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.283-536_283-526del others(11): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433120 | ||||||
| chr17:82433120 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0267 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.283-536_283-516del others(21): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433120 | ||||||
| chr17:82433120 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283-528_283-506del others(23): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433120 | ||||||
| chr17:82433122 | A | T | 2 | a0001c0001t0001g0037 a0001c0003t0001g0119 |
2 | HG03209.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.283-536A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433122 | |||||||
| chr17:82433122 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.283-534_283-516del others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433122 | ||||||
| chr17:82433122 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.283-528_283-508del others(21): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433122 | ||||||
| chr17:82433124 | A | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0180 a0001c0003t0001g0119 others(3): Show |
6 | HG02486.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-534A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433124 | |||||||
| chr17:82433124 | ATATATTT others(10): Show |
A | 1 | a0001c0003t0001g0130 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.283-532_283-516del others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433124 | ||||||
| chr17:82433124 | ATATATTT others(12): Show |
A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0064 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.283-528_283-510del others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433124 | ||||||
| chr17:82433124 | ATATATTT others(24): Show |
A | 1 | a0001c0007t0001g0024 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.283-532_283-502del others(31): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433124 | ||||||
| chr17:82433125 | TA | T | 3 | a0002c0002t0001g0002 a0002c0002t0001g0106 a0002c0002t0001g0114 |
3 | HG00639.hp1 HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.283-532delA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433125 | |||||||
| chr17:82433126 | A | T | 7 | a0001c0001t0001g0037 a0001c0003t0001g0119 a0002c0002t0001g0002 others(4): Show |
11 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-532A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433126 | |||||||
| chr17:82433126 | ATATTTTT others(10): Show |
A | 1 | a0001c0001t0001g0266 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.283-528_283-512del others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433126 | ||||||
| chr17:82433126 | ATATTTTT others(22): Show |
A | 1 | a0001c0007t0001g0162 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.283-530_283-502del others(29): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433126 | ||||||
| chr17:82433127 | TA | T | 7 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0094 others(4): Show |
7 | HG00140.hp2 HG00733.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-530delA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433127 | |||||||
| chr17:82433128 | A | ATATATAT others(17): Show |
1 | a0002c0004t0001g0223 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(24): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0021 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(16): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(10): Show |
1 | a0002c0004t0001g0291 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.283-529_283-528ins others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(7): Show |
1 | a0002c0002t0001g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(14): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(11): Show |
1 | a0002c0010t0001g0224 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(18): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(12): Show |
1 | a0001c0003t0001g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATATAT others(11): Show |
1 | a0002c0004t0001g0225 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(18): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATATTTTT others(8): Show |
1 | a0001c0003t0001g0110 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283-529_283-528ins others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283-523_283-514dup others(10): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | ATTTTTTT others(7): Show |
1 | a0002c0002t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.283-527_283-514dup others(14): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | A | T | 18 | a0001c0001t0001g0037 a0001c0003t0001g0020 a0001c0003t0001g0119 others(15): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-530A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433128 | |||||||
| chr17:82433128 | AT | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
95 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.283-514delT | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | ATTT | A | 19 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0030 others(16): Show |
20 | HG01099.hp1 HG01934.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.283-516_283-514del others(3): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | ATTTTT | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0066 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-518_283-514del others(5): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | ATTTTTTT | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0057 others(9): Show |
12 | HG01167.hp1 HG01516.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-520_283-514del others(7): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0068 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.283-524_283-514del others(11): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | ATTTTTTT others(6): Show |
A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0001t0001g0217 others(3): Show |
6 | HG01496.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-526_283-514del others(13): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433128 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.283-528_283-514del others(15): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 82433128 | ||||||
| chr17:82433129 | T | TA | 25 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0030 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-529_283-528ins others(1): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433129 | |||||||
| chr17:82433129 | T | TATA | 9 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0165 others(6): Show |
9 | HG00558.hp2 HG01192.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-529_283-528ins others(3): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433129 | |||||||
| chr17:82433130 | T | A | 9 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0082 others(6): Show |
10 | HG01361.hp1 HG01517.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-528T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433130 | |||||||
| chr17:82433131 | T | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(110): Show |
125 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.283-527T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433131 | |||||||
| chr17:82433132 | T | A | 3 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0002c0002t0001g0097 |
3 | HG03490.hp2 HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.283-526T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433132 | |||||||
| chr17:82433133 | T | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(124): Show |
143 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.283-525T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433133 | |||||||
| chr17:82433134 | T | A | 3 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0002c0002t0001g0097 |
3 | HG03490.hp2 HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.283-524T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433134 | |||||||
| chr17:82433135 | T | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(131): Show |
151 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.283-523T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433135 | |||||||
| chr17:82433137 | T | A | 145 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(142): Show |
162 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.283-521T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433137 | |||||||
| chr17:82433139 | T | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(145): Show |
165 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.283-519T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433139 | |||||||
| chr17:82433141 | T | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(147): Show |
167 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.283-517T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433141 | |||||||
| chr17:82433143 | T | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
18 | HG01884.hp1 HG02040.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.283-515T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433143 | |||||||
| chr17:82433144 | T | A | 1 | a0002c0002t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.283-514T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433144 | |||||||
| chr17:82433144 | TA | T | 3 | a0002c0002t0001g0098 a0002c0002t0001g0099 a0008c0018t0001g0092 |
3 | HG02280.hp2 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.283-513delA | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433144 | |||||||
| chr17:82433145 | A | T | 8 | a0001c0001t0001g0037 a0001c0003t0001g0117 a0002c0002t0001g0002 others(5): Show |
9 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-513A>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433145 | |||||||
| chr17:82433161 | T | A | 145 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(142): Show |
165 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.283-497T>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433161 | |||||||
| chr17:82433268 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-390G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433268 | |||||||
| chr17:82433322 | A | G | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283-336A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433322 | |||||||
| chr17:82433497 | A | C | 4 | a0002c0002t0001g0095 a0002c0002t0001g0096 a0002c0002t0001g0097 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-161A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433497 | |||||||
| chr17:82433507 | C | A | 1 | a0001c0003t0001g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.283-151C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433507 | |||||||
| chr17:82433610 | C | T | 5 | a0002c0004t0001g0015 a0002c0004t0001g0040 a0002c0004t0001g0041 others(2): Show |
6 | HG02145.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-48C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433610 | |||||||
| chr17:82433653 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18974.hp1 NA18989.hp1 |
splice_region_variant&intron_variant | LOW | c.283-5C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 4/12 | chr17 | 82433653 | |||||||
| chr17:82433833 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.447+11T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82433833 | |||||||
| chr17:82433948 | ATCCAACA others(76): Show |
A | 1 | a0001c0003t0001g0140 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.447+143_447+225del others(83): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 82433948 | ||||||
| chr17:82433997 | C | G | 1 | a0002c0002t0001g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.447+175C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82433997 | |||||||
| chr17:82433998 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0181 a0001c0001t0001g0197 |
4 | NA18964.hp1 NA18977.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+176G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82433998 | |||||||
| chr17:82434005 | G | A | 185 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(182): Show |
238 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.447+183G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434005 | |||||||
| chr17:82434029 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.447+207G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434029 | |||||||
| chr17:82434029 | G | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(128): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.447+207G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434029 | |||||||
| chr17:82434081 | A | G | 1 | a0001c0003t0001g0140 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.447+259A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434081 | |||||||
| chr17:82434111 | C | T | 4 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0002c0002t0001g0084 others(1): Show |
4 | HG00099.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+289C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434111 | |||||||
| chr17:82434112 | G | A | 3 | a0002c0002t0001g0107 a0002c0002t0001g0111 a0002c0002t0001g0116 |
3 | HG01074.hp2 HG01978.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.447+290G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434112 | |||||||
| chr17:82434123 | G | T | 1 | a0001c0003t0001g0126 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.447+301G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434123 | |||||||
| chr17:82434207 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.447+385C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434207 | |||||||
| chr17:82434433 | A | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+611A>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434433 | |||||||
| chr17:82434457 | G | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(130): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.447+635G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434457 | |||||||
| chr17:82434530 | T | C | 3 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0091 |
5 | HG03491.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+708T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434530 | |||||||
| chr17:82434554 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.447+732T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434554 | |||||||
| chr17:82434667 | G | A | 2 | a0002c0002t0001g0098 a0002c0002t0001g0099 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.447+845G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434667 | |||||||
| chr17:82434698 | C | T | 8 | a0002c0002t0001g0115 a0002c0002t0001g0120 a0002c0002t0001g0121 others(5): Show |
8 | HG00408.hp1 HG02135.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+876C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434698 | |||||||
| chr17:82434766 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.448-923A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434766 | |||||||
| chr17:82434768 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.448-921G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434768 | |||||||
| chr17:82434924 | C | T | 222 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(219): Show |
278 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.448-765C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82434924 | |||||||
| chr17:82435018 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.448-671G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435018 | |||||||
| chr17:82435052 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0201 |
2 | NA18942.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.448-637G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435052 | |||||||
| chr17:82435208 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.448-481C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435208 | |||||||
| chr17:82435209 | A | G | 12 | a0001c0007t0001g0024 a0001c0007t0001g0162 a0002c0002t0001g0149 others(9): Show |
15 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.448-480A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435209 | |||||||
| chr17:82435292 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.448-397G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435292 | |||||||
| chr17:82435385 | G | A | 5 | a0001c0001t0001g0163 a0001c0001t0001g0180 a0001c0001t0001g0192 others(2): Show |
5 | HG00733.hp2 HG01243.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-304G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435385 | |||||||
| chr17:82435535 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0002g0032 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448-154C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435535 | |||||||
| chr17:82435543 | G | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.448-146G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435543 | |||||||
| chr17:82435545 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.448-144G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435545 | |||||||
| chr17:82435597 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0181 a0001c0001t0001g0197 |
4 | NA18964.hp1 NA18977.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-92G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435597 | |||||||
| chr17:82435616 | C | T | 1 | a0001c0013t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.448-73C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435616 | |||||||
| chr17:82435642 | G | A | 1 | a0002c0004t0001g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.448-47G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435642 | |||||||
| chr17:82435655 | G | C | 1 | a0002c0002t0001g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.448-34G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435655 | |||||||
| chr17:82435682 | C | T | 1 | a0003c0008t0001g0023 | 2 | HG01243.hp2 HG02717.hp2 |
splice_region_variant&intron_variant | LOW | c.448-7C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 5/12 | chr17 | 82435682 | |||||||
| chr17:82435944 | G | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.631+72G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82435944 | |||||||
| chr17:82436027 | G | A | 1 | a0001c0003t0001g0138 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.631+155G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436027 | |||||||
| chr17:82436027 | GCCTGAGT others(6): Show |
G | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.631+159_631+171del others(13): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 82436027 | ||||||
| chr17:82436204 | G | A | 219 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(216): Show |
275 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.631+332G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436204 | |||||||
| chr17:82436295 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.632-372C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436295 | |||||||
| chr17:82436412 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.632-255C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436412 | |||||||
| chr17:82436430 | C | G | 5 | a0001c0001t0001g0163 a0001c0001t0001g0180 a0001c0001t0001g0192 others(2): Show |
5 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-237C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436430 | |||||||
| chr17:82436467 | A | G | 5 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.632-200A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436467 | |||||||
| chr17:82436654 | G | T | 188 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(185): Show |
241 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.632-13G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 6/12 | chr17 | 82436654 | |||||||
| chr17:82436888 | TGCCTCGG others(4): Show |
T | 1 | a0001c0003t0001g0132 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.703+154_703+164del others(11): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 82436888 | ||||||
| chr17:82436955 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.704-213G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/12 | chr17 | 82436955 | |||||||
| chr17:82436997 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0003t0001g0080 others(3): Show |
7 | HG00738.hp1 HG01081.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-171G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/12 | chr17 | 82436997 | |||||||
| chr17:82437007 | C | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(130): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.704-161C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/12 | chr17 | 82437007 | |||||||
| chr17:82437047 | C | G | 6 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
7 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-121C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 7/12 | chr17 | 82437047 | |||||||
| chr17:82437435 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+72G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82437435 | |||||||
| chr17:82437581 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(128): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.899+218G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82437581 | |||||||
| chr17:82437602 | A | G | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.899+239A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82437602 | |||||||
| chr17:82437625 | C | CTG | 20 | a0001c0003t0001g0102 a0002c0002t0001g0006 a0002c0002t0001g0009 others(17): Show |
25 | HG00642.hp1 HG01074.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.899+284_899+285dup others(2): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 82437625 | ||||||
| chr17:82437625 | CTG | C | 30 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0059 others(27): Show |
33 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.899+284_899+285del others(2): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 82437625 | ||||||
| chr17:82437625 | CTGTGTGT others(1): Show |
C | 186 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(183): Show |
239 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.899+278_899+285del others(8): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 82437625 | ||||||
| chr17:82437970 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.899+607C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82437970 | |||||||
| chr17:82438080 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.899+717C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438080 | |||||||
| chr17:82438132 | G | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(5): Show |
8 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.899+769G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438132 | |||||||
| chr17:82438191 | TCA | T | 10 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(7): Show |
12 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.899+832_899+833del others(2): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 82438191 | ||||||
| chr17:82438345 | G | A | 1 | a0001c0013t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.899+982G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438345 | |||||||
| chr17:82438657 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.900-974G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438657 | |||||||
| chr17:82438800 | C | T | 1 | a0008c0018t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.900-831C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438800 | |||||||
| chr17:82438801 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-830G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438801 | |||||||
| chr17:82438812 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0002g0032 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.900-819C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438812 | |||||||
| chr17:82438815 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.900-816C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438815 | |||||||
| chr17:82438900 | C | T | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG01099.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.900-731C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438900 | |||||||
| chr17:82438925 | C | T | 184 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(181): Show |
237 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.900-706C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438925 | |||||||
| chr17:82438929 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.900-702G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438929 | |||||||
| chr17:82438958 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0253 |
2 | HG00735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.900-673C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82438958 | |||||||
| chr17:82439032 | A | G | 1 | a0001c0003t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.900-599A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439032 | |||||||
| chr17:82439191 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.900-440A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439191 | |||||||
| chr17:82439261 | G | C | 1 | a0002c0002t0001g0022 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.900-370G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439261 | |||||||
| chr17:82439296 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
12 | HG00738.hp1 HG01081.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.900-335C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439296 | |||||||
| chr17:82439373 | G | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
9 | HG00738.hp1 HG01081.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-258G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439373 | |||||||
| chr17:82439401 | C | A | 1 | a0001c0001t0003g0177 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.900-230C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439401 | |||||||
| chr17:82439406 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0003t0001g0080 others(3): Show |
7 | HG00738.hp1 HG01081.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.900-225C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439406 | |||||||
| chr17:82439518 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.900-113C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439518 | |||||||
| chr17:82439571 | C | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.900-60C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439571 | |||||||
| chr17:82439578 | G | A | 8 | a0002c0002t0001g0022 a0002c0002t0001g0078 a0002c0002t0001g0089 others(5): Show |
9 | HG01106.hp1 HG01123.hp1 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-53G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439578 | |||||||
| chr17:82439601 | C | T | 1 | a0001c0003t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.900-30C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439601 | |||||||
| chr17:82439608 | A | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(224): Show |
284 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.900-23A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 8/12 | chr17 | 82439608 | |||||||
| chr17:82439755 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.982+42C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439755 | |||||||
| chr17:82439774 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.982+61G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439774 | |||||||
| chr17:82439836 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0268 |
2 | NA18941.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.982+123G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439836 | |||||||
| chr17:82439870 | G | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0277 |
2 | NA18975.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.982+157G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439870 | |||||||
| chr17:82439892 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0001g0269 |
3 | NA18948.hp2 NA18963.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.982+179G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439892 | |||||||
| chr17:82439951 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.982+238C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439951 | |||||||
| chr17:82439986 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.982+273G>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82439986 | |||||||
| chr17:82440060 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0268 |
2 | NA18941.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.982+347C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440060 | |||||||
| chr17:82440087 | G | A | 4 | a0001c0001t0001g0274 a0001c0003t0001g0125 a0001c0003t0001g0127 others(1): Show |
4 | HG00597.hp2 NA18942.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+374G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440087 | |||||||
| chr17:82440135 | G | A | 10 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(7): Show |
12 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.982+422G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440135 | |||||||
| chr17:82440161 | G | A | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.982+448G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440161 | |||||||
| chr17:82440179 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.982+466G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440179 | |||||||
| chr17:82440202 | C | CTG | 10 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(7): Show |
12 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.982+498_982+499dup others(2): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 82440202 | ||||||
| chr17:82440276 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.982+563C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440276 | |||||||
| chr17:82440349 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0281 |
3 | NA18950.hp1 NA18989.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.982+636A>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440349 | |||||||
| chr17:82440368 | C | T | 1 | a0001c0001t0001g0031 | 2 | NA18959.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.983-629C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440368 | |||||||
| chr17:82440409 | G | T | 8 | a0002c0004t0001g0058 a0002c0004t0001g0205 a0002c0004t0001g0206 others(5): Show |
8 | HG02109.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.983-588G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440409 | |||||||
| chr17:82440498 | C | T | 1 | a0001c0003t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.983-499C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440498 | |||||||
| chr17:82440577 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0002g0032 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.983-420G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440577 | |||||||
| chr17:82440703 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0005g0062 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.983-294G>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440703 | |||||||
| chr17:82440707 | C | T | 5 | a0001c0001t0001g0163 a0001c0001t0001g0180 a0001c0001t0001g0192 others(2): Show |
5 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.983-290C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440707 | |||||||
| chr17:82440708 | G | A | 1 | a0001c0003t0001g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.983-289G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440708 | |||||||
| chr17:82440836 | C | G | 5 | a0001c0001t0001g0163 a0001c0001t0001g0180 a0001c0001t0001g0192 others(2): Show |
5 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.983-161C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 9/12 | chr17 | 82440836 | |||||||
| chr17:82441107 | C | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0091 |
3 | HG03491.hp2 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1061+32C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 10/12 | chr17 | 82441107 | |||||||
| chr17:82441126 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1062-39G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 10/12 | chr17 | 82441126 | |||||||
| chr17:82441160 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01884.hp2 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.1062-5C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 10/12 | chr17 | 82441160 | |||||||
| chr17:82441161 | G | A | 1 | a0002c0002t0001g0153 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.1062-4G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 10/12 | chr17 | 82441161 | |||||||
| chr17:82441292 | GTGGGTGA others(12): Show |
G | 1 | a0002c0002t0001g0100 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1163+31_1163+49del others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 82441292 | ||||||
| chr17:82441305 | G | A | 3 | a0002c0002t0001g0109 a0002c0002t0001g0112 a0002c0002t0001g0114 |
3 | HG00639.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1163+39G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441305 | |||||||
| chr17:82441317 | C | T | 187 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(184): Show |
240 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.1163+51C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441317 | |||||||
| chr17:82441329 | A | AGGGGGCA others(10): Show |
2 | a0001c0001t0001g0254 a0001c0001t0001g0262 |
2 | HG00423.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1163+66_1163+82dup others(17): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 82441329 | ||||||
| chr17:82441333 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163+67G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441333 | |||||||
| chr17:82441345 | T | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0263 |
2 | NA18948.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1163+79T>C | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441345 | |||||||
| chr17:82441461 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1163+195G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441461 | |||||||
| chr17:82441476 | AGGGGCAG others(22): Show |
A | 10 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(7): Show |
12 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1163+222_1163+250d others(31): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 82441476 | ||||||
| chr17:82441541 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1164-259C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441541 | |||||||
| chr17:82441553 | GGGCAGGT others(10): Show |
G | 1 | a0002c0002t0001g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164-232_1164-216d others(19): Show |
HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 82441553 | ||||||
| chr17:82441632 | C | G | 1 | a0001c0001t0001g0226 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1164-168C>G | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441632 | |||||||
| chr17:82441632 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1164-168C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 11/12 | chr17 | 82441632 | |||||||
| chr17:82442012 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1253+123C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 12/12 | chr17 | 82442012 | |||||||
| chr17:82442046 | C | T | 2 | a0001c0007t0001g0024 a0001c0007t0001g0162 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1254-131C>T | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 12/12 | chr17 | 82442046 | |||||||
| chr17:82442047 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254-130G>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 12/12 | chr17 | 82442047 | |||||||
| chr17:82442077 | C | A | 10 | a0002c0002t0001g0149 a0002c0004t0001g0015 a0002c0004t0001g0016 others(7): Show |
12 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1254-100C>A | HEXD | ENSG00000169660.17 | transcript | ENST00000327949.15 | protein_coding | 12/12 | chr17 | 82442077 |