Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7485 |
| ensemblid | ENSG00000182093.16 |
| hgncid | 12790 |
| symbol | GET1 |
| name | guided entry of tail-anchored proteins factor 1 |
| refseq_nuc | NM_004627.6 |
| refseq_prot | NP_004618.2 |
| ensembl_nuc | ENST00000649170.1 |
| ensembl_prot | ENSP00000496813.1 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 39380326 |
| end | 39397889 |
| strand | + |
| ver | v1.2 |
| region | chr21:39380326-39397889 |
| region5000 | chr21:39375326-39402889 |
| regionname0 | GET1_chr21_39380326_39397889 |
| regionname5000 | GET1_chr21_39375326_39402889 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 174 | 333 | 81 | 68 | 128 | 18 | 36 | 96 | GET1_chr21_39375326_39402889 | GET1 | MSSAA others(169): Show |
chr21 | 39375326 | 39402889 |
| a0002 | 0/0 | 174 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | MSSAA others(169): Show |
chr21 | 39375326 | 39402889 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 522 | 333 | 81 | 68 | 128 | 18 | 36 | GET1_chr21_39375326_39402889 | GET1 | ATGAG others(517): Show |
chr21 | 39375326 | 39402889 | ||
| a0002c0002 | 0/0 | 522 | 5 | 5 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | ATGAG others(517): Show |
chr21 | 39375326 | 39402889 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1539 | 212 | 33 | 45 | 94 | 13 | 27 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0002 | 1/1 | 1534 | 101 | 36 | 19 | 32 | 4 | 8 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1529): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0003 | 0/0 | 1534 | 6 | 5 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1529): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0004 | 0/0 | 1534 | 3 | 3 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1529): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0006 | 0/0 | 1534 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1529): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0007 | 0/0 | 1539 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0009 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1529): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0010 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0011 | 0/0 | 1534 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1529): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0012 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0014 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0015 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0001c0001t0016 | 0/0 | 1539 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0002c0002t0005 | 0/0 | 1539 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0002c0002t0008 | 0/0 | 1539 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| a0002c0002t0013 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | GTTGT others(1534): Show |
chr21 | 39375326 | 39402889 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 63 | 7 | 11 | 33 | 4 | 8 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0002 | 1/0 | 14 | 1 | 4 | 6 | 0 | 2 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0003 | 0/0 | 13 | 9 | 2 | 2 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0012 | 0/1 | 4 | 0 | 1 | 0 | 1 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0003g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0014g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0002c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0002c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0002c0002t0008g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| a0002c0002t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0001 | EUR | GBR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | IBS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02148 | hp2 | a0001 | c0001 | t0016 | g0001 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02717 | hp2 | a0002 | c0002 | t0005 | g0140 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02886 | hp2 | a0002 | c0002 | t0008 | g0042 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03209 | hp1 | a0002 | c0002 | t0013 | g0064 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0030 | SAS | BEB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18906 | hp1 | a0002 | c0002 | t0005 | g0087 | AFR | YRI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | YRI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18944 | hp1 | a0001 | c0001 | t0015 | g0128 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | LWK | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0142 | AFR | LWK | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ASW | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | TSI | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02109 | hp1 | a0002 | c0002 | t0008 | g0042 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | USA | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | LWK | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0012 | REF | REF | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | GET1_chr21_39375326_39402889 | GET1 | chr21 | 39375326 | 39402889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39391828 | G | A | 1 | a0002 | 5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
missense_variant | MODERATE | c.328G>A | p.Val110Ile | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/5 | 387/1534 | 328/525 | 110/174 | chr21 | 39391828 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39380335 | G | A | 1 | a0001c0001t0009 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/5 | 50 | chr21 | 39380335 | ||||||
| chr21:39396988 | C | G | 1 | a0002c0002t0008 | 2 | HG02109.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 49 | chr21 | 39396988 | ||||||
| chr21:39397016 | T | C | 1 | a0001c0001t0010 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 77 | chr21 | 39397016 | ||||||
| chr21:39397037 | G | A | 1 | a0001c0001t0004 | 3 | HG02622.hp2 HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*98G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 98 | chr21 | 39397037 | ||||||
| chr21:39397091 | G | T | 6 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(3): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*152G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 152 | chr21 | 39397091 | ||||||
| chr21:39397118 | C | T | 1 | a0001c0001t0016 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 179 | chr21 | 39397118 | ||||||
| chr21:39397156 | G | A | 1 | a0001c0001t0007 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*217G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 217 | chr21 | 39397156 | ||||||
| chr21:39397202 | G | A | 1 | a0002c0002t0005 | 2 | HG02717.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*263G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 263 | chr21 | 39397202 | ||||||
| chr21:39397222 | T | C | 1 | a0001c0001t0014 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*283T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 283 | chr21 | 39397222 | ||||||
| chr21:39397246 | T | A | 1 | a0001c0001t0011 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307T>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 307 | chr21 | 39397246 | ||||||
| chr21:39397364 | A | G | 7 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(4): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*425A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 425 | chr21 | 39397364 | ||||||
| chr21:39397378 | G | A | 1 | a0001c0001t0015 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 439 | chr21 | 39397378 | ||||||
| chr21:39397685 | G | GATTAA | 10 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(7): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*747_*751dupATTAA | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 752 | INFO_REALIGN_3_PRIME | chr21 | 39397685 | |||||
| chr21:39397881 | T | C | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(6): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*942T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 5/5 | 942 | chr21 | 39397881 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39380720 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.102+234T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39380720 | |||||||
| chr21:39380733 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.102+247G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39380733 | |||||||
| chr21:39380741 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.102+255C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39380741 | |||||||
| chr21:39380767 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.102+281A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39380767 | |||||||
| chr21:39380825 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0151 |
3 | HG01257.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.102+339C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39380825 | |||||||
| chr21:39381081 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.102+595C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39381081 | |||||||
| chr21:39381441 | A | C | 1 | a0001c0001t0002g0083 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.102+955A>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39381441 | |||||||
| chr21:39381554 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102+1068C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39381554 | |||||||
| chr21:39381707 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.102+1221G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39381707 | |||||||
| chr21:39381898 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0085 |
4 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+1412C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39381898 | |||||||
| chr21:39381992 | G | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0149 |
5 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+1506G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39381992 | |||||||
| chr21:39382057 | CT | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0086 a0001c0001t0002g0045 others(2): Show |
6 | HG01169.hp2 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+1586delT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39382057 | ||||||
| chr21:39382168 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.102+1682C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382168 | |||||||
| chr21:39382178 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.102+1692C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382178 | |||||||
| chr21:39382209 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+1723C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382209 | |||||||
| chr21:39382508 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18947.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.102+2022A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382508 | |||||||
| chr21:39382638 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0081 a0001c0001t0002g0153 |
4 | HG01070.hp1 HG01081.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2152A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382638 | |||||||
| chr21:39382768 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.102+2282C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382768 | |||||||
| chr21:39382984 | T | G | 1 | a0001c0001t0002g0043 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.102+2498T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39382984 | |||||||
| chr21:39383015 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.102+2529G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383015 | |||||||
| chr21:39383019 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.102+2533C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383019 | |||||||
| chr21:39383100 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0002g0079 |
5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+2614A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383100 | |||||||
| chr21:39383115 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.102+2629G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383115 | |||||||
| chr21:39383146 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.102+2660A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383146 | |||||||
| chr21:39383156 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102+2670G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383156 | |||||||
| chr21:39383189 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.102+2703T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383189 | |||||||
| chr21:39383196 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.102+2710T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383196 | |||||||
| chr21:39383197 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.102+2711G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383197 | |||||||
| chr21:39383205 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.102+2719T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383205 | |||||||
| chr21:39383234 | T | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0002c0002t0005g0087 others(1): Show |
4 | HG02717.hp2 HG02922.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2748T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383234 | |||||||
| chr21:39383237 | T | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0002c0002t0005g0087 others(1): Show |
4 | HG02717.hp2 HG02922.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2751T>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383237 | |||||||
| chr21:39383240 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.102+2754C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383240 | |||||||
| chr21:39383250 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0136 others(1): Show |
7 | HG03486.hp1 HG03486.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+2764A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383250 | |||||||
| chr21:39383374 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102+2888C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383374 | |||||||
| chr21:39383574 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.102+3088A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383574 | |||||||
| chr21:39383574 | ACCCAGCT others(155): Show |
G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0041 |
4 | HG00621.hp2 HG00642.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+3088_102+3249d others(2): Show |
GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383574 | |||||||
| chr21:39383949 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0059 a0001c0001t0002g0060 others(1): Show |
12 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.102+3463G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383949 | |||||||
| chr21:39383961 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102+3475G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383961 | |||||||
| chr21:39383971 | C | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02080.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.102+3485C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39383971 | |||||||
| chr21:39384032 | C | A | 1 | a0001c0001t0001g0019 | 3 | HG03490.hp2 HG03492.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.102+3546C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384032 | |||||||
| chr21:39384035 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.102+3549C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384035 | |||||||
| chr21:39384040 | C | CT | 8 | a0001c0001t0001g0091 a0001c0001t0001g0133 a0001c0001t0001g0139 others(5): Show |
17 | HG01257.hp1 HG01258.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.102+3567dupT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39384040 | ||||||
| chr21:39384068 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.102+3582T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384068 | |||||||
| chr21:39384290 | T | C | 1 | a0001c0001t0002g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.102+3804T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384290 | |||||||
| chr21:39384359 | C | A | 2 | a0001c0001t0006g0061 a0001c0001t0006g0065 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.102+3873C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384359 | |||||||
| chr21:39384386 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0130 a0001c0001t0001g0131 |
9 | HG00639.hp1 HG01081.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.102+3900A>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384386 | |||||||
| chr21:39384415 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.102+3929C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384415 | |||||||
| chr21:39384435 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.102+3949T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384435 | |||||||
| chr21:39384564 | A | AT | 3 | a0001c0001t0002g0005 a0001c0001t0002g0059 a0001c0001t0009g0005 |
11 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.102+4095dupT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39384564 | ||||||
| chr21:39384564 | AT | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.102+4095delT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39384564 | ||||||
| chr21:39384564 | ATT | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG01070.hp2 HG01515.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+4094_102+4095d others(4): Show |
GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39384564 | ||||||
| chr21:39384601 | A | G | 1 | a0001c0001t0004g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102+4115A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384601 | |||||||
| chr21:39384634 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0149 others(2): Show |
8 | HG00639.hp2 HG01975.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+4148G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384634 | |||||||
| chr21:39384749 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.102+4263G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384749 | |||||||
| chr21:39384755 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0014g0030 |
2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.102+4269T>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384755 | |||||||
| chr21:39384837 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0078 |
4 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+4351C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384837 | |||||||
| chr21:39384881 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102+4395G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39384881 | |||||||
| chr21:39385065 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0149 |
5 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+4579C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385065 | |||||||
| chr21:39385125 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.102+4639C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385125 | |||||||
| chr21:39385126 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0096 |
7 | HG01168.hp1 HG01169.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+4640A>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385126 | |||||||
| chr21:39385663 | G | T | 2 | a0001c0001t0002g0076 a0001c0001t0002g0152 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.103-5035G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385663 | |||||||
| chr21:39385840 | G | A | 4 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(1): Show |
6 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-4858G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385840 | |||||||
| chr21:39385901 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0057 a0001c0001t0002g0058 others(1): Show |
7 | HG00408.hp2 NA18960.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-4797C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385901 | |||||||
| chr21:39385951 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0015g0128 |
2 | NA18944.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.103-4747C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385951 | |||||||
| chr21:39385961 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.103-4737G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39385961 | |||||||
| chr21:39386039 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0149 |
4 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-4659C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386039 | |||||||
| chr21:39386046 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103-4652C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386046 | |||||||
| chr21:39386047 | T | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.103-4651T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386047 | |||||||
| chr21:39386062 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.103-4636C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386062 | |||||||
| chr21:39386157 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0149 |
5 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-4541T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386157 | |||||||
| chr21:39386334 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.103-4364A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386334 | |||||||
| chr21:39386448 | G | T | 1 | a0001c0001t0002g0056 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.103-4250G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386448 | |||||||
| chr21:39386550 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.103-4148A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386550 | |||||||
| chr21:39386772 | G | A | 1 | a0002c0002t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103-3926G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39386772 | |||||||
| chr21:39386849 | C | CT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(89): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.103-3837dupT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39386849 | ||||||
| chr21:39387133 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0082 |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-3565T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387133 | |||||||
| chr21:39387134 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.103-3564A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387134 | |||||||
| chr21:39387137 | G | A | 1 | a0001c0001t0006g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103-3561G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387137 | |||||||
| chr21:39387337 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.103-3361C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387337 | |||||||
| chr21:39387487 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0122 |
5 | HG00558.hp1 HG00673.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-3211A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387487 | |||||||
| chr21:39387685 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.103-3013C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387685 | |||||||
| chr21:39387691 | T | TC | 20 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
27 | HG00438.hp1 HG00621.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.103-2997dupC | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39387691 | ||||||
| chr21:39387699 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.103-2999C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387699 | |||||||
| chr21:39387701 | C | A | 4 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(1): Show |
6 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2997C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387701 | |||||||
| chr21:39387701 | C | G | 1 | a0001c0001t0002g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-2997C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387701 | |||||||
| chr21:39387702 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0085 others(3): Show |
9 | HG00639.hp2 HG01975.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-2996A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387702 | |||||||
| chr21:39387763 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.103-2935G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387763 | |||||||
| chr21:39387933 | C | G | 2 | a0001c0001t0002g0076 a0001c0001t0002g0152 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.103-2765C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387933 | |||||||
| chr21:39387956 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.103-2742T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387956 | |||||||
| chr21:39387959 | G | A | 1 | a0001c0001t0002g0043 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.103-2739G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387959 | |||||||
| chr21:39387966 | A | G | 1 | a0001c0001t0002g0043 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.103-2732A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39387966 | |||||||
| chr21:39388003 | G | A | 4 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(1): Show |
6 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2695G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388003 | |||||||
| chr21:39388188 | A | G | 4 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(1): Show |
6 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2510A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388188 | |||||||
| chr21:39388233 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.103-2465T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388233 | |||||||
| chr21:39388328 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0149 |
5 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-2370C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388328 | |||||||
| chr21:39388333 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0102 |
3 | HG01123.hp2 HG01192.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.103-2365G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388333 | |||||||
| chr21:39388609 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.103-2089C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388609 | |||||||
| chr21:39388679 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(104): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.103-2019A>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388679 | |||||||
| chr21:39388820 | C | G | 3 | a0001c0001t0002g0012 a0001c0001t0002g0048 a0001c0001t0002g0099 |
5 | HG00280.hp1 HG01074.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-1878C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388820 | |||||||
| chr21:39388820 | C | T | 1 | a0002c0002t0005g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.103-1878C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388820 | |||||||
| chr21:39388850 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18942.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.103-1848G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388850 | |||||||
| chr21:39388856 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.103-1842G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39388856 | |||||||
| chr21:39389130 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.103-1568G>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389130 | |||||||
| chr21:39389305 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.103-1393A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389305 | |||||||
| chr21:39389381 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.103-1317A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389381 | |||||||
| chr21:39389467 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103-1231T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389467 | |||||||
| chr21:39389584 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.103-1114C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389584 | |||||||
| chr21:39389619 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.103-1079T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389619 | |||||||
| chr21:39389653 | G | T | 1 | a0001c0001t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.103-1045G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389653 | |||||||
| chr21:39389666 | G | T | 2 | a0001c0001t0006g0061 a0001c0001t0006g0065 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.103-1032G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389666 | |||||||
| chr21:39389816 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-882C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389816 | |||||||
| chr21:39389837 | C | T | 2 | a0002c0002t0008g0042 a0002c0002t0013g0064 |
3 | HG02109.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.103-861C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39389837 | |||||||
| chr21:39390042 | G | GT | 20 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0027 others(17): Show |
32 | HG01169.hp2 HG01257.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.103-636dupT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39390042 | ||||||
| chr21:39390042 | G | GTT | 4 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0149 others(1): Show |
6 | HG00639.hp2 HG01975.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-637_103-636dup others(2): Show |
GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39390042 | ||||||
| chr21:39390042 | GT | G | 26 | a0001c0001t0001g0097 a0001c0001t0002g0003 a0001c0001t0002g0009 others(23): Show |
48 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.103-636delT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | 39390042 | ||||||
| chr21:39390170 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.103-528C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390170 | |||||||
| chr21:39390202 | A | G | 5 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(2): Show |
7 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-496A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390202 | |||||||
| chr21:39390329 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(90): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.103-369G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390329 | |||||||
| chr21:39390542 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.103-156C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390542 | |||||||
| chr21:39390544 | T | C | 1 | a0001c0001t0012g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103-154T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390544 | |||||||
| chr21:39390611 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103-87G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390611 | |||||||
| chr21:39390631 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.103-67G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390631 | |||||||
| chr21:39390642 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(16): Show |
39 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.103-56G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390642 | |||||||
| chr21:39390677 | C | G | 5 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(2): Show |
7 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-21C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 1/4 | chr21 | 39390677 | |||||||
| chr21:39391226 | G | T | 2 | a0002c0002t0005g0087 a0002c0002t0005g0140 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.268+363G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 2/4 | chr21 | 39391226 | |||||||
| chr21:39391227 | A | G | 2 | a0002c0002t0005g0087 a0002c0002t0005g0140 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.268+364A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 2/4 | chr21 | 39391227 | |||||||
| chr21:39391486 | A | G | 2 | a0002c0002t0005g0087 a0002c0002t0005g0140 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.269-283A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 2/4 | chr21 | 39391486 | |||||||
| chr21:39391568 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0098 a0001c0001t0001g0100 |
4 | HG01243.hp2 HG01978.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-201G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 2/4 | chr21 | 39391568 | |||||||
| chr21:39391703 | G | C | 1 | a0001c0001t0003g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.269-66G>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 2/4 | chr21 | 39391703 | |||||||
| chr21:39391753 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.269-16C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 2/4 | chr21 | 39391753 | |||||||
| chr21:39391895 | C | A | 1 | a0002c0002t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.336+59C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39391895 | |||||||
| chr21:39391895 | C | T | 2 | a0002c0002t0005g0087 a0002c0002t0005g0140 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.336+59C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39391895 | |||||||
| chr21:39391924 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0136 |
2 | HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.336+88G>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39391924 | |||||||
| chr21:39391969 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(104): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.336+133T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39391969 | |||||||
| chr21:39392060 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.336+224T>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392060 | |||||||
| chr21:39392080 | C | T | 4 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(1): Show |
6 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.336+244C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392080 | |||||||
| chr21:39392123 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(91): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.336+287G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392123 | |||||||
| chr21:39392467 | G | T | 2 | a0002c0002t0008g0042 a0002c0002t0013g0064 |
3 | HG02109.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.336+631G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392467 | |||||||
| chr21:39392513 | A | AT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.337-652dupT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | 39392513 | ||||||
| chr21:39392523 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.337-643G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392523 | |||||||
| chr21:39392786 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.337-380C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392786 | |||||||
| chr21:39392895 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.337-271A>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 3/4 | chr21 | 39392895 | |||||||
| chr21:39393375 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+95C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393375 | |||||||
| chr21:39393403 | C | T | 4 | a0002c0002t0005g0087 a0002c0002t0005g0140 a0002c0002t0008g0042 others(1): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+123C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393403 | |||||||
| chr21:39393585 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.451+305A>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393585 | |||||||
| chr21:39393625 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.451+345G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393625 | |||||||
| chr21:39393671 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG00438.hp1 HG00621.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+391T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393671 | |||||||
| chr21:39393792 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.451+512G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393792 | |||||||
| chr21:39393881 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18942.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.451+601C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39393881 | |||||||
| chr21:39394122 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.451+842G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394122 | |||||||
| chr21:39394255 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.451+975G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394255 | |||||||
| chr21:39394255 | G | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.451+975G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394255 | |||||||
| chr21:39394321 | G | C | 4 | a0002c0002t0005g0087 a0002c0002t0005g0140 a0002c0002t0008g0042 others(1): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1041G>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394321 | |||||||
| chr21:39394564 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.451+1284T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394564 | |||||||
| chr21:39394596 | C | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0059 a0001c0001t0002g0060 others(1): Show |
12 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.451+1316C>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394596 | |||||||
| chr21:39394684 | T | C | 1 | a0001c0001t0002g0043 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.451+1404T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394684 | |||||||
| chr21:39394937 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.451+1657A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394937 | |||||||
| chr21:39394968 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0136 |
2 | HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.451+1688C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39394968 | |||||||
| chr21:39395202 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-1664T>C | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39395202 | |||||||
| chr21:39395368 | AT | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.452-1484delT | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr21 | 39395368 | ||||||
| chr21:39395444 | A | G | 5 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0078 others(2): Show |
7 | HG01346.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-1422A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39395444 | |||||||
| chr21:39395524 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.452-1342C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39395524 | |||||||
| chr21:39395564 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.452-1302A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39395564 | |||||||
| chr21:39396259 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0002g0071 a0002c0002t0005g0087 others(1): Show |
4 | HG00642.hp1 HG02717.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-607G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396259 | |||||||
| chr21:39396260 | G | T | 1 | a0001c0001t0002g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.452-606G>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396260 | |||||||
| chr21:39396306 | C | T | 2 | a0001c0001t0006g0061 a0001c0001t0006g0065 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.452-560C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396306 | |||||||
| chr21:39396344 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.452-522C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396344 | |||||||
| chr21:39396356 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0109 others(1): Show |
5 | HG01884.hp1 HG02145.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-510A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396356 | |||||||
| chr21:39396390 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.452-476C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396390 | |||||||
| chr21:39396438 | C | T | 2 | a0002c0002t0008g0042 a0002c0002t0013g0064 |
3 | HG02109.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.452-428C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396438 | |||||||
| chr21:39396497 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.452-369C>T | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396497 | |||||||
| chr21:39396635 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.452-231G>A | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396635 | |||||||
| chr21:39396685 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.452-162delA | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr21 | 39396685 | ||||||
| chr21:39396756 | C | G | 1 | a0001c0001t0002g0054 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.452-110C>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396756 | |||||||
| chr21:39396796 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.452-70A>G | GET1 | ENSG00000182093.16 | transcript | ENST00000649170.1 | protein_coding | 4/4 | chr21 | 39396796 |