Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57467 |
| ensemblid | ENSG00000010282.15 |
| hgncid | 13242 |
| symbol | HHATL |
| name | hedgehog acyltransferase like |
| refseq_nuc | NM_020707.4 |
| refseq_prot | NP_065758.3 |
| ensembl_nuc | ENST00000441594.6 |
| ensembl_prot | ENSP00000405423.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 42692663 |
| end | 42702798 |
| strand | - |
| ver | v1.2 |
| region | chr3:42692663-42702798 |
| region5000 | chr3:42687663-42707798 |
| regionname0 | HHATL_chr3_42692663_42702798 |
| regionname5000 | HHATL_chr3_42687663_42707798 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 504 | 269 | 60 | 54 | 113 | 10 | 32 | 83 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0002 | 1/0 | 504 | 129 | 29 | 27 | 55 | 3 | 14 | 47 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0003 | 0/0 | 504 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0004 | 0/0 | 504 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0005 | 0/0 | 504 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0006 | 0/0 | 504 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0007 | 0/0 | 504 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0008 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0009 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0010 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0011 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| a0012 | 0/1 | 504 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | MGIKT others(499): Show |
chr3 | 42687663 | 42707798 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1512 | 246 | 51 | 54 | 100 | 10 | 31 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0001c0005 | 0/0 | 1512 | 12 | 0 | 0 | 12 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0001c0006 | 0/0 | 1512 | 5 | 4 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0001c0008 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0001c0012 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0001c0019 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0001c0020 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0002c0002 | 1/0 | 1512 | 83 | 14 | 19 | 32 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0002c0003 | 0/0 | 1512 | 29 | 0 | 6 | 23 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0002c0004 | 0/0 | 1512 | 14 | 14 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0002c0011 | 0/0 | 1512 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0002c0017 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0003c0007 | 0/0 | 1512 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0004c0009 | 0/0 | 1512 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0005c0010 | 0/0 | 1512 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0006c0022 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0007c0015 | 0/0 | 1512 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0008c0016 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0009c0021 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0010c0013 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0011c0018 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 | ||
| a0012c0014 | 0/1 | 1512 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ATGGG others(1507): Show |
chr3 | 42687663 | 42707798 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1836 | 246 | 51 | 54 | 100 | 10 | 31 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0001c0005t0001 | 0/0 | 1836 | 12 | 0 | 0 | 12 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0001c0006t0001 | 0/0 | 1836 | 5 | 4 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0001c0008t0001 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0001c0012t0001 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0001c0019t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0001c0020t0001 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0002c0002t0001 | 1/0 | 1836 | 83 | 14 | 19 | 32 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0002c0003t0001 | 0/0 | 1836 | 29 | 0 | 6 | 23 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0002c0004t0001 | 0/0 | 1836 | 13 | 13 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0002c0004t0002 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0002c0011t0001 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0002c0017t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0003c0007t0001 | 0/0 | 1836 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0004c0009t0001 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0005c0010t0001 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0006c0022t0001 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0007c0015t0001 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0008c0016t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0009c0021t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0010c0013t0001 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0011c0018t0001 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| a0012c0014t0001 | 0/1 | 1836 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | ACTCT others(1831): Show |
chr3 | 42687663 | 42707798 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 96 | 15 | 18 | 52 | 3 | 8 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0002 | 0/0 | 45 | 2 | 7 | 19 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0013 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0005t0001g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0006t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0008t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0012t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0019t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0001c0020t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0004 | 1/0 | 19 | 1 | 11 | 0 | 0 | 6 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0005 | 0/0 | 12 | 7 | 2 | 1 | 0 | 2 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0009 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0010 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0011 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0003t0001g0003 | 0/0 | 26 | 0 | 6 | 20 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0004t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0004t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0004t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0004t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0011t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0002c0017t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0003c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0003c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0003c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0004c0009t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0005c0010t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0006c0022t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0007c0015t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0008c0016t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0009c0021t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0010c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0011c0018t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| a0012c0014t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00323 | hp1 | a0006 | c0022 | t0001 | g0061 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00544 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00609 | hp1 | a0001 | c0005 | t0001 | g0110 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00609 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00738 | hp1 | a0004 | c0009 | t0001 | g0035 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01070 | hp1 | a0005 | c0010 | t0001 | g0037 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01167 | hp1 | a0002 | c0011 | t0001 | g0033 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01169 | hp1 | a0002 | c0011 | t0001 | g0033 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01175 | hp1 | a0005 | c0010 | t0001 | g0037 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01175 | hp2 | a0004 | c0009 | t0001 | g0035 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01361 | hp2 | a0007 | c0015 | t0001 | g0085 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0088 | EUR | IBS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01891 | hp1 | a0002 | c0004 | t0001 | g0031 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0047 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02056 | hp1 | a0001 | c0005 | t0001 | g0109 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02523 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02615 | hp1 | a0002 | c0004 | t0001 | g0022 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02647 | hp2 | a0003 | c0007 | t0001 | g0056 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02717 | hp1 | a0002 | c0004 | t0002 | g0117 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02723 | hp2 | a0003 | c0007 | t0001 | g0051 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02809 | hp1 | a0003 | c0007 | t0001 | g0050 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02818 | hp1 | a0001 | c0012 | t0001 | g0032 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02886 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02895 | hp2 | a0001 | c0008 | t0001 | g0029 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02897 | hp2 | a0001 | c0008 | t0001 | g0029 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0031 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0027 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03041 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0022 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03130 | hp2 | a0002 | c0004 | t0001 | g0071 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03209 | hp1 | a0009 | c0021 | t0001 | g0112 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0022 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03490 | hp1 | a0001 | c0020 | t0001 | g0072 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0012 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0105 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18906 | hp2 | a0002 | c0017 | t0001 | g0045 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18941 | hp1 | a0001 | c0006 | t0001 | g0041 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18962 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18973 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18975 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18980 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18998 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19007 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19009 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19043 | hp1 | a0001 | c0019 | t0001 | g0078 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19064 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19074 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19087 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19090 | hp1 | a0011 | c0018 | t0001 | g0055 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19240 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ASW | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02109 | hp2 | a0008 | c0016 | t0001 | g0083 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02486 | hp2 | a0001 | c0012 | t0001 | g0032 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18955 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA18955 | hp2 | a0010 | c0013 | t0001 | g0064 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20300 | hp1 | a0002 | c0004 | t0001 | g0074 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA20300 | hp2 | a0001 | c0006 | t0001 | g0027 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0046 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| homoSapiens_chm13v2 | hp1 | a0012 | c0014 | t0001 | g0067 | REF | REF | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0004 | REF | REF | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42692759 | G | C | 1 | a0007 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1507C>G | p.Pro503Ala | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 12/12 | 1740/1836 | 1507/1515 | 503/504 | chr3 | 42692759 | |||
| chr3:42692803 | C | T | 1 | a0005 | 2 | HG01070.hp1 HG01175.hp1 |
missense_variant | MODERATE | c.1463G>A | p.Arg488Gln | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 12/12 | 1696/1836 | 1463/1515 | 488/504 | chr3 | 42692803 | |||
| chr3:42693095 | G | C | 1 | a0008 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1372C>G | p.Arg458Gly | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 11/12 | 1605/1836 | 1372/1515 | 458/504 | chr3 | 42693095 | |||
| chr3:42693658 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
missense_variant | MODERATE | c.1207A>G | p.Met403Val | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/12 | 1440/1836 | 1207/1515 | 403/504 | chr3 | 42693658 | |||
| chr3:42693745 | C | T | 1 | a0012 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1120G>A | p.Ala374Thr | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/12 | 1353/1836 | 1120/1515 | 374/504 | chr3 | 42693745 | |||
| chr3:42697041 | G | T | 1 | a0004 | 2 | HG00738.hp1 HG01175.hp2 |
missense_variant | MODERATE | c.970C>A | p.Pro324Thr | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/12 | 1203/1836 | 970/1515 | 324/504 | chr3 | 42697041 | |||
| chr3:42697547 | C | A | 1 | a0011 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.826G>T | p.Asp276Tyr | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/12 | 1059/1836 | 826/1515 | 276/504 | chr3 | 42697547 | |||
| chr3:42698898 | C | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.293G>A | p.Arg98His | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/12 | 526/1836 | 293/1515 | 98/504 | chr3 | 42698898 | |||
| chr3:42699061 | C | A | 1 | a0009 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.259G>T | p.Ala87Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/12 | 492/1836 | 259/1515 | 87/504 | chr3 | 42699061 | |||
| chr3:42699084 | G | A | 1 | a0006 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.236C>T | p.Ala79Val | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/12 | 469/1836 | 236/1515 | 79/504 | chr3 | 42699084 | |||
| chr3:42700801 | G | C | 1 | a0003 | 3 | HG02647.hp2 HG02723.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.26C>G | p.Ala9Gly | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/12 | 259/1836 | 26/1515 | 9/504 | chr3 | 42700801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42693782 | A | G | 16 | a0001c0001 a0001c0005 a0001c0006 others(13): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
synonymous_variant | LOW | c.1083T>C | p.Ala361Ala | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/12 | 1316/1836 | 1083/1515 | 361/504 | chr3 | 42693782 | |||
| chr3:42697102 | C | T | 2 | a0001c0008 a0002c0003 |
31 | HG01081.hp2 HG01358.hp1 HG01978.hp2 others(28): Show |
synonymous_variant | LOW | c.909G>A | p.Ala303Ala | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/12 | 1142/1836 | 909/1515 | 303/504 | chr3 | 42697102 | |||
| chr3:42697536 | G | A | 2 | a0001c0006 a0002c0017 |
6 | HG01891.hp2 HG02976.hp1 NA18906.hp2 others(3): Show |
synonymous_variant | LOW | c.837C>T | p.Phe279Phe | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/12 | 1070/1836 | 837/1515 | 279/504 | chr3 | 42697536 | |||
| chr3:42697548 | G | A | 1 | a0001c0019 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.825C>T | p.Ser275Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/12 | 1058/1836 | 825/1515 | 275/504 | chr3 | 42697548 | |||
| chr3:42698244 | G | A | 1 | a0001c0020 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.591C>T | p.His197His | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/12 | 824/1836 | 591/1515 | 197/504 | chr3 | 42698244 | |||
| chr3:42698777 | G | C | 1 | a0002c0011 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.414C>G | p.Pro138Pro | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/12 | 647/1836 | 414/1515 | 138/504 | chr3 | 42698777 | |||
| chr3:42698792 | C | T | 1 | a0001c0005 | 12 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(9): Show |
synonymous_variant | LOW | c.399G>A | p.Ser133Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/12 | 632/1836 | 399/1515 | 133/504 | chr3 | 42698792 | |||
| chr3:42699077 | G | A | 1 | a0001c0012 | 2 | HG02486.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.243C>T | p.Ser81Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/12 | 476/1836 | 243/1515 | 81/504 | chr3 | 42699077 | |||
| chr3:42700767 | A | G | 1 | a0003c0007 | 3 | HG02647.hp2 HG02723.hp2 HG02809.hp1 |
synonymous_variant | LOW | c.60T>C | p.Ser20Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/12 | 293/1836 | 60/1515 | 20/504 | chr3 | 42700767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42702591 | G | A | 1 | a0002c0004t0002 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/12 | 1765 | chr3 | 42702591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42692953 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1391-78G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 11/11 | chr3 | 42692953 | |||||||
| chr3:42692953 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1391-78G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 11/11 | chr3 | 42692953 | |||||||
| chr3:42693258 | C | A | 11 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0014 others(8): Show |
32 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-40G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693258 | |||||||
| chr3:42693335 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1249-117C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693335 | |||||||
| chr3:42693562 | G | GC | 17 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
25 | HG01070.hp1 HG01074.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248+54dupG | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693562 | |||||||
| chr3:42693568 | C | A | 1 | a0001c0001t0001g0036 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1248+49G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693568 | |||||||
| chr3:42694131 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1047-313A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694131 | |||||||
| chr3:42694159 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1047-341A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694159 | |||||||
| chr3:42694349 | C | G | 1 | a0005c0010t0001g0037 | 2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1047-531G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694349 | |||||||
| chr3:42694395 | A | G | 1 | a0001c0001t0001g0021 | 4 | HG03139.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-577T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694395 | |||||||
| chr3:42694470 | A | G | 3 | a0002c0002t0001g0010 a0002c0002t0001g0080 a0008c0016t0001g0083 |
9 | HG00099.hp2 HG00733.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1047-652T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694470 | |||||||
| chr3:42694471 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0077 a0001c0001t0001g0096 others(6): Show |
13 | HG01070.hp1 HG01175.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1047-653C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694471 | |||||||
| chr3:42694538 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047-720G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694538 | |||||||
| chr3:42694665 | C | T | 1 | a0001c0005t0001g0110 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1047-847G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694665 | |||||||
| chr3:42694704 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1047-886T>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694704 | |||||||
| chr3:42694706 | G | A | 3 | a0001c0001t0001g0026 a0001c0006t0001g0041 a0001c0006t0001g0046 |
4 | NA18941.hp1 NA18992.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-888C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694706 | |||||||
| chr3:42694813 | C | T | 1 | a0001c0001t0001g0015 | 5 | HG00621.hp1 NA18947.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-995G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694813 | |||||||
| chr3:42694909 | T | C | 1 | a0001c0006t0001g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1047-1091A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694909 | |||||||
| chr3:42694943 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0057 others(1): Show |
5 | HG02559.hp2 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1125T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694943 | |||||||
| chr3:42695001 | GTGCCTAG others(5): Show |
G | 2 | a0002c0004t0001g0022 a0002c0004t0001g0071 |
4 | HG02615.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-1195_1047-118 others(16): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695001 | |||||||
| chr3:42695165 | C | A | 10 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0014 others(7): Show |
31 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1047-1347G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695165 | |||||||
| chr3:42695227 | C | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1047-1409G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695227 | |||||||
| chr3:42695293 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047-1475C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695293 | |||||||
| chr3:42695492 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0097 a0003c0007t0001g0050 others(2): Show |
5 | HG02258.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+1350G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695492 | |||||||
| chr3:42695537 | T | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0038 others(5): Show |
15 | HG00639.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046+1305A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695537 | |||||||
| chr3:42695537 | T | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(89): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1046+1305A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695537 | |||||||
| chr3:42695545 | C | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(59): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1046+1297G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695545 | |||||||
| chr3:42695553 | A | G | 1 | a0002c0003t0001g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1046+1289T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695553 | |||||||
| chr3:42695749 | C | T | 11 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0040 others(8): Show |
53 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1046+1093G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695749 | |||||||
| chr3:42695754 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(96): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1046+1088A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695754 | |||||||
| chr3:42695989 | C | T | 1 | a0002c0002t0001g0018 | 4 | HG02109.hp1 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046+853G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695989 | |||||||
| chr3:42696249 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0008t0001g0029 |
5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+593C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696249 | |||||||
| chr3:42696305 | G | A | 23 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0057 others(20): Show |
51 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1046+537C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696305 | |||||||
| chr3:42696387 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(69): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1046+455G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696387 | |||||||
| chr3:42696509 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0057 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1046+333G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696509 | |||||||
| chr3:42696535 | C | T | 2 | a0001c0001t0001g0038 a0009c0021t0001g0112 |
3 | HG03209.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1046+307G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696535 | |||||||
| chr3:42696547 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(96): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1046+295G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696547 | |||||||
| chr3:42696644 | C | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1046+198G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696644 | |||||||
| chr3:42696651 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1046+191G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696651 | |||||||
| chr3:42696805 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(42): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1046+37C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696805 | |||||||
| chr3:42696898 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1011-21C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/11 | chr3 | 42696898 | |||||||
| chr3:42696978 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1010+23G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/11 | chr3 | 42696978 | |||||||
| chr3:42697299 | TG | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0042 |
4 | NA19064.hp2 NA19067.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-155delC | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697299 | |||||||
| chr3:42697310 | C | T | 5 | a0002c0004t0001g0012 a0002c0004t0001g0022 a0002c0004t0001g0031 others(2): Show |
13 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.866-165G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697310 | |||||||
| chr3:42697317 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0044 others(1): Show |
10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.866-172A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697317 | |||||||
| chr3:42697320 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0044 others(1): Show |
10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.866-175A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697320 | |||||||
| chr3:42697336 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.865+172C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697336 | |||||||
| chr3:42697337 | A | G | 1 | a0001c0001t0001g0021 | 4 | HG03139.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+171T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697337 | |||||||
| chr3:42697342 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0044 others(1): Show |
10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+166C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697342 | |||||||
| chr3:42697389 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0044 others(1): Show |
10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+119G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697389 | |||||||
| chr3:42697414 | G | T | 1 | a0002c0004t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+94C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697414 | |||||||
| chr3:42697440 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0008t0001g0029 |
5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+68C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697440 | |||||||
| chr3:42697443 | G | A | 1 | a0002c0002t0001g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.865+65C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697443 | |||||||
| chr3:42697471 | C | T | 5 | a0002c0004t0001g0012 a0002c0004t0001g0022 a0002c0004t0001g0031 others(2): Show |
13 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.865+37G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697471 | |||||||
| chr3:42697472 | G | A | 1 | a0002c0011t0001g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.865+36C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697472 | |||||||
| chr3:42697496 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.865+12G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697496 | |||||||
| chr3:42697724 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0057 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.694-45C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697724 | |||||||
| chr3:42697755 | T | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0038 others(36): Show |
79 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.694-76A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697755 | |||||||
| chr3:42697794 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.694-115G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697794 | |||||||
| chr3:42697854 | G | A | 5 | a0002c0004t0001g0012 a0002c0004t0001g0022 a0002c0004t0001g0031 others(2): Show |
13 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.694-175C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697854 | |||||||
| chr3:42697906 | G | A | 14 | a0001c0001t0001g0030 a0001c0001t0001g0052 a0001c0001t0001g0057 others(11): Show |
24 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.694-227C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697906 | |||||||
| chr3:42698030 | A | G | 1 | a0003c0007t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.693+112T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42698030 | |||||||
| chr3:42698458 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0092 |
3 | HG01243.hp1 HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.484-107G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698458 | |||||||
| chr3:42698459 | C | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0044 others(1): Show |
10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-108G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698459 | |||||||
| chr3:42698467 | C | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.484-116G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698467 | |||||||
| chr3:42698533 | GA | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(49): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.483+174delT | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698533 | |||||||
| chr3:42698545 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.483+163A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698545 | |||||||
| chr3:42698922 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0115 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.289-20A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/11 | chr3 | 42698922 | |||||||
| chr3:42698942 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.289-40C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/11 | chr3 | 42698942 | |||||||
| chr3:42699000 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
14 | HG00280.hp2 HG01074.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.288+32C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/11 | chr3 | 42699000 | |||||||
| chr3:42699204 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.175-59G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699204 | |||||||
| chr3:42699289 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0044 |
8 | HG00639.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-144A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699289 | |||||||
| chr3:42699325 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0008t0001g0029 |
5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-180G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699325 | |||||||
| chr3:42699325 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0057 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.175-180G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699325 | |||||||
| chr3:42699368 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0058 others(17): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.175-223G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699368 | |||||||
| chr3:42699436 | G | T | 4 | a0001c0006t0001g0027 a0001c0006t0001g0046 a0001c0006t0001g0047 others(1): Show |
5 | HG01891.hp2 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-291C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699436 | |||||||
| chr3:42699443 | C | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.175-298G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699443 | |||||||
| chr3:42699734 | G | GACCCTGG others(17): Show |
1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.174_174+23dupGGTAG others(19): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699734 | |||||||
| chr3:42699743 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.174+15T>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699743 | |||||||
| chr3:42699903 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.107-78G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42699903 | |||||||
| chr3:42700006 | C | CTG | 3 | a0001c0001t0001g0026 a0001c0006t0001g0041 a0002c0002t0001g0014 |
8 | NA18941.hp1 NA18964.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-183_107-182dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700006 | |||||||
| chr3:42700020 | G | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(38): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.107-195C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700020 | |||||||
| chr3:42700080 | C | CTG | 23 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0038 others(20): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.107-257_107-256dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700080 | |||||||
| chr3:42700080 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.107-255G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700080 | |||||||
| chr3:42700082 | G | C | 4 | a0001c0006t0001g0027 a0001c0006t0001g0046 a0001c0006t0001g0047 others(1): Show |
5 | HG01891.hp2 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-257C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700082 | |||||||
| chr3:42700096 | G | C | 3 | a0002c0002t0001g0009 a0002c0002t0001g0043 a0011c0018t0001g0055 |
9 | HG01123.hp1 HG01975.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-271C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700096 | |||||||
| chr3:42700118 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-293T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700118 | |||||||
| chr3:42700122 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-297G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700122 | |||||||
| chr3:42700124 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-299C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700124 | |||||||
| chr3:42700128 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-303G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700128 | |||||||
| chr3:42700134 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-309G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700134 | |||||||
| chr3:42700135 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-310A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700135 | |||||||
| chr3:42700136 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-311G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700136 | |||||||
| chr3:42700137 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-312A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700137 | |||||||
| chr3:42700141 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-316A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700141 | |||||||
| chr3:42700142 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-317C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700142 | |||||||
| chr3:42700143 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-318A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700143 | |||||||
| chr3:42700149 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-324A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700149 | |||||||
| chr3:42700150 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-325G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700150 | |||||||
| chr3:42700156 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-331G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700156 | |||||||
| chr3:42700158 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-333T>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700158 | |||||||
| chr3:42700163 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-338A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700163 | |||||||
| chr3:42700164 | C | CTG | 19 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0058 others(16): Show |
66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.107-341_107-340dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | |||||||
| chr3:42700164 | C | CTGTG | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0006t0001g0027 others(5): Show |
11 | HG00323.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-343_107-340dup others(4): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | |||||||
| chr3:42700164 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-339G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | |||||||
| chr3:42700164 | CTG | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(46): Show |
198 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.107-341_107-340del others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | |||||||
| chr3:42700182 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-357C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700182 | |||||||
| chr3:42700183 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-358A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700183 | |||||||
| chr3:42700185 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-360A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700185 | |||||||
| chr3:42700196 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-371C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700196 | |||||||
| chr3:42700200 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-375C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700200 | |||||||
| chr3:42700201 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-376A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700201 | |||||||
| chr3:42700206 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-381T>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700206 | |||||||
| chr3:42700208 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-383T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700208 | |||||||
| chr3:42700212 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-387G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700212 | |||||||
| chr3:42700236 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-411T>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700236 | |||||||
| chr3:42700237 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-412A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700237 | |||||||
| chr3:42700239 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-414G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700239 | |||||||
| chr3:42700250 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-425G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700250 | |||||||
| chr3:42700251 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-426A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700251 | |||||||
| chr3:42700253 | T | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0102 |
3 | HG01070.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107-428A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700253 | |||||||
| chr3:42700261 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-436A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700261 | |||||||
| chr3:42700262 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-437C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700262 | |||||||
| chr3:42700263 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-438A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700263 | |||||||
| chr3:42700266 | GGGTCCAG others(3): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+445_107-442del others(10): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700266 | |||||||
| chr3:42700283 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+438A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700283 | |||||||
| chr3:42700284 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+437C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700284 | |||||||
| chr3:42700287 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+434A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700287 | |||||||
| chr3:42700288 | A | ATG | 3 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0002c0002t0001g0053 |
5 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+431_106+432dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700288 | |||||||
| chr3:42700288 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+433T>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700288 | |||||||
| chr3:42700293 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+428A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700293 | |||||||
| chr3:42700294 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+427C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700294 | |||||||
| chr3:42700300 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.106+421C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700300 | |||||||
| chr3:42700301 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+420A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700301 | |||||||
| chr3:42700310 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+411C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700310 | |||||||
| chr3:42700318 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+403C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700318 | |||||||
| chr3:42700345 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.106+376A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700345 | |||||||
| chr3:42700346 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+375G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700346 | |||||||
| chr3:42700360 | CTG | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0026 others(46): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.106+359_106+360del others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700360 | |||||||
| chr3:42700380 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+341G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700380 | |||||||
| chr3:42700387 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+334A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700387 | |||||||
| chr3:42700392 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+329C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700392 | |||||||
| chr3:42700398 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+323T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700398 | |||||||
| chr3:42700402 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+319G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700402 | |||||||
| chr3:42700405 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+316C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700405 | |||||||
| chr3:42700412 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+309C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700412 | |||||||
| chr3:42700415 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+306A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700415 | |||||||
| chr3:42700416 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+305G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700416 | |||||||
| chr3:42700417 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+304A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700417 | |||||||
| chr3:42700418 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+303C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700418 | |||||||
| chr3:42700421 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+300A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700421 | |||||||
| chr3:42700429 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+292A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700429 | |||||||
| chr3:42700437 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+284G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700437 | |||||||
| chr3:42700439 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+282C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700439 | |||||||
| chr3:42700442 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+279G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700442 | |||||||
| chr3:42700443 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+278A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700443 | |||||||
| chr3:42700444 | C | CTG | 5 | a0001c0001t0001g0023 a0001c0012t0001g0032 a0001c0019t0001g0078 others(2): Show |
10 | HG01070.hp1 HG01175.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+275_106+276dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700444 | |||||||
| chr3:42700444 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+277G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700444 | |||||||
| chr3:42700444 | CTG | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0026 others(46): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.106+275_106+276del others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700444 | |||||||
| chr3:42700462 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+259C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700462 | |||||||
| chr3:42700623 | G | T | 1 | a0002c0004t0002g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.106+98C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700623 | |||||||
| chr3:42700645 | G | A | 1 | a0001c0001t0001g0020 | 4 | HG01074.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+76C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700645 | |||||||
| chr3:42700659 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0057 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.106+62C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700659 | |||||||
| chr3:42700664 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.106+57G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700664 | |||||||
| chr3:42700874 | T | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0057 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-13-35A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42700874 | |||||||
| chr3:42700876 | C | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-13-37G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42700876 | |||||||
| chr3:42700913 | C | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-13-74G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42700913 | |||||||
| chr3:42701015 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0103 |
3 | HG01257.hp1 HG01258.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-13-176C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701015 | |||||||
| chr3:42701027 | C | T | 1 | a0001c0005t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-13-188G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701027 | |||||||
| chr3:42701078 | C | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(40): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-13-239G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701078 | |||||||
| chr3:42701146 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0039 others(20): Show |
79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-13-307C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701146 | |||||||
| chr3:42701199 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-13-360C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701199 | |||||||
| chr3:42701239 | T | C | 1 | a0001c0001t0001g0006 | 10 | HG01496.hp1 HG01928.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-400A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701239 | |||||||
| chr3:42701240 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-13-401C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701240 | |||||||
| chr3:42701256 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02145.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-13-417C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701256 | |||||||
| chr3:42701398 | C | A | 1 | a0001c0001t0001g0016 | 5 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-559G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701398 | |||||||
| chr3:42701575 | T | TGGGGCCA others(3): Show |
7 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0104 others(4): Show |
39 | HG00621.hp1 HG01081.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.-13-746_-13-737dup others(10): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701575 | |||||||
| chr3:42701575 | TGGGGCCA others(3): Show |
T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0006t0001g0041 others(1): Show |
5 | HG02809.hp2 NA18941.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-746_-13-737del others(10): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701575 | |||||||
| chr3:42701649 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0008t0001g0029 |
5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-810G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701649 | |||||||
| chr3:42701652 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(49): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-13-813G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701652 | |||||||
| chr3:42701702 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-13-863G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701702 | |||||||
| chr3:42701962 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-14+617G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701962 | |||||||
| chr3:42701983 | G | T | 2 | a0001c0001t0001g0026 a0001c0006t0001g0041 |
3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-14+596C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701983 | |||||||
| chr3:42702053 | G | A | 4 | a0001c0005t0001g0007 a0001c0005t0001g0109 a0001c0005t0001g0110 others(1): Show |
13 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14+526C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702053 | |||||||
| chr3:42702091 | T | C | 1 | a0005c0010t0001g0037 | 2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-14+488A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702091 | |||||||
| chr3:42702259 | T | C | 2 | a0001c0001t0001g0038 a0009c0021t0001g0112 |
3 | HG03209.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-14+320A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702259 | |||||||
| chr3:42702366 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02145.hp1 HG03471.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+213C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702366 | |||||||
| chr3:42702375 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14+204G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702375 | |||||||
| chr3:42702476 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0039 |
7 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+103C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702476 |