| geneid | 57493 |
|---|---|
| ensemblid | ENSG00000173706.15 |
| hgncid | 29227 |
| symbol | HEG1 |
| name | heart development protein with EGF like domains 1 |
| refseq_nuc | NM_020733.2 |
| refseq_prot | NP_065784.1 |
| ensembl_nuc | ENST00000311127.9 |
| ensembl_prot | ENSP00000311502.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 124965710 |
| end | 125055997 |
| strand | - |
| ver | v1.2 |
| region | chr3:124965710-125055997 |
| region5000 | chr3:124960710-125060997 |
| regionname0 | HEG1_chr3_124965710_125055997 |
| regionname5000 | HEG1_chr3_124960710_125060997 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1381 | 106 | 8 | 21 | 52 | 3 | 21 | 41 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002 | 0/0 | 1387 | 34 | 2 | 1 | 28 | 0 | 3 | 24 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003 | 1/0 | 1381 | 29 | 6 | 2 | 16 | 1 | 3 | 13 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004 | 0/0 | 1387 | 25 | 8 | 2 | 13 | 0 | 2 | 9 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005 | 0/0 | 1387 | 17 | 5 | 4 | 8 | 0 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006 | 0/0 | 1381 | 16 | 4 | 3 | 7 | 1 | 1 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007 | 0/0 | 1381 | 13 | 5 | 3 | 3 | 0 | 2 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008 | 0/0 | 1386 | 11 | 1 | 2 | 8 | 0 | 0 | 7 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009 | 0/0 | 1381 | 10 | 2 | 5 | 3 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010 | 0/0 | 1380 | 8 | 0 | 2 | 6 | 0 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0011 | 0/0 | 1381 | 7 | 0 | 5 | 0 | 0 | 2 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012 | 0/0 | 1381 | 6 | 1 | 4 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013 | 0/0 | 1387 | 5 | 4 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0014 | 0/0 | 1382 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0015 | 0/0 | 1387 | 4 | 0 | 2 | 2 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0016 | 0/0 | 1382 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0017 | 0/0 | 1381 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0018 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0019 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0020 | 0/0 | 1381 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0021 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0022 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0023 | 0/0 | 1380 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0024 | 0/0 | 1388 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0025 | 0/0 | 1382 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0026 | 0/0 | 1388 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0027 | 0/0 | 1381 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0028 | 0/0 | 1381 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0029 | 0/0 | 1381 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0030 | 0/0 | 1380 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0031 | 0/0 | 1388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0032 | 0/0 | 1388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0033 | 0/0 | 1381 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0034 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0035 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0036 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0037 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0038 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0039 | 0/0 | 1387 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0040 | 0/0 | 1387 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0041 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0042 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0043 | 0/0 | 1381 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0044 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0045 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0046 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0047 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0048 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0049 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0050 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0051 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0052 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0053 | 0/0 | 1381 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0054 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0055 | 0/0 | 1381 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0056 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0057 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0058 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0059 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4146 | 48 | 5 | 7 | 32 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0002 | 0/1 | 4146 | 48 | 1 | 11 | 18 | 3 | 14 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0003 | 0/0 | 4164 | 27 | 1 | 1 | 22 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0004 | 0/0 | 4146 | 24 | 6 | 1 | 16 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0005 | 0/0 | 4164 | 15 | 3 | 1 | 11 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0006 | 0/0 | 4146 | 15 | 3 | 3 | 7 | 1 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0007 | 0/0 | 4164 | 13 | 5 | 3 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0008 | 0/0 | 4146 | 7 | 0 | 5 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0009 | 0/0 | 4146 | 7 | 2 | 3 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0010 | 0/0 | 4146 | 6 | 0 | 1 | 2 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0011 | 0/0 | 4146 | 6 | 3 | 2 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0012 | 0/0 | 4161 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0013 | 0/0 | 4161 | 5 | 0 | 2 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0014 | 0/0 | 4164 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0015 | 0/0 | 4146 | 5 | 0 | 1 | 3 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0016 | 0/0 | 4143 | 4 | 0 | 0 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0017 | 0/0 | 4164 | 4 | 0 | 2 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0018 | 0/0 | 4146 | 4 | 1 | 2 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0019 | 0/0 | 4149 | 4 | 0 | 0 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0020 | 0/0 | 4146 | 3 | 2 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0021 | 0/0 | 4143 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0022 | 0/0 | 4143 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0023 | 0/0 | 4146 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0024 | 0/0 | 4146 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0025 | 0/0 | 4146 | 3 | 1 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0026 | 0/0 | 4146 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0027 | 0/0 | 4146 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0028 | 0/0 | 4164 | 2 | 0 | 0 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0029 | 0/0 | 4149 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0030 | 0/0 | 4149 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0031 | 0/0 | 4167 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0032 | 0/0 | 4146 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0033 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0034 | 1/0 | 4146 | 2 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0035 | 0/0 | 4164 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0036 | 0/0 | 4146 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0037 | 0/0 | 4146 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0038 | 0/0 | 4164 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0039 | 0/0 | 4164 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0040 | 0/0 | 4164 | 2 | 1 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0041 | 0/0 | 4146 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0042 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0043 | 0/0 | 4146 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0044 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0045 | 0/0 | 4146 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0046 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0047 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0048 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0049 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0050 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0051 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0052 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0053 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0054 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0055 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0056 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0057 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0058 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0059 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0060 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0061 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0062 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0063 | 0/0 | 4146 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0064 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0065 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0066 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0067 | 0/0 | 4146 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0068 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0069 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0070 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0071 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0072 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0073 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0074 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0075 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0076 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0077 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0078 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0079 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0080 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0081 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0082 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0083 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0084 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0085 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0086 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0087 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0088 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0089 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0090 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0091 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0092 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0093 | 0/0 | 4146 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0094 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0095 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0096 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| c0097 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 5056 | 21 | 0 | 5 | 9 | 0 | 6 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0002 | 0/0 | 5058 | 15 | 1 | 2 | 12 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0003 | 0/0 | 5059 | 14 | 0 | 0 | 14 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0004 | 0/0 | 5050 | 14 | 1 | 2 | 9 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0005 | 0/0 | 5049 | 12 | 1 | 5 | 4 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0006 | 0/0 | 5051 | 9 | 1 | 2 | 5 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0007 | 0/0 | 5058 | 8 | 0 | 1 | 5 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0008 | 0/0 | 5052 | 8 | 0 | 2 | 6 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0009 | 0/0 | 5058 | 7 | 1 | 1 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0010 | 0/0 | 5059 | 7 | 4 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0011 | 0/0 | 5057 | 6 | 3 | 1 | 1 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0012 | 0/0 | 5058 | 6 | 1 | 0 | 4 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0013 | 0/0 | 5052 | 6 | 1 | 1 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0014 | 0/0 | 5052 | 6 | 1 | 2 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0015 | 0/0 | 5057 | 5 | 0 | 0 | 4 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0016 | 0/0 | 5057 | 5 | 0 | 1 | 3 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0017 | 0/0 | 5050 | 5 | 0 | 1 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0018 | 0/0 | 5051 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0019 | 0/0 | 5059 | 4 | 2 | 0 | 1 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0020 | 0/0 | 5057 | 4 | 0 | 2 | 0 | 1 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0021 | 0/0 | 5057 | 4 | 0 | 0 | 2 | 2 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0022 | 0/0 | 5059 | 4 | 4 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0023 | 0/0 | 5058 | 4 | 3 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0024 | 0/0 | 5057 | 4 | 0 | 0 | 1 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0025 | 0/0 | 5052 | 4 | 1 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0026 | 0/0 | 5051 | 4 | 4 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0027 | 0/0 | 5050 | 4 | 0 | 1 | 2 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0028 | 0/0 | 5052 | 4 | 0 | 1 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0029 | 0/0 | 5059 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0030 | 0/0 | 5055 | 3 | 0 | 0 | 2 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0031 | 0/0 | 5057 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0032 | 0/0 | 5056 | 3 | 0 | 0 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0033 | 0/0 | 5058 | 3 | 0 | 1 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0034 | 0/0 | 5051 | 3 | 0 | 3 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0035 | 0/0 | 5051 | 3 | 1 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0036 | 0/0 | 5050 | 3 | 0 | 3 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0037 | 0/0 | 5052 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0038 | 0/0 | 5050 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0039 | 0/0 | 5058 | 2 | 1 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0040 | 0/0 | 5059 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0041 | 0/0 | 5057 | 2 | 1 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0042 | 0/0 | 5057 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0043 | 0/0 | 5059 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0044 | 0/0 | 5058 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0045 | 0/0 | 5057 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0046 | 0/0 | 5056 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0047 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0048 | 0/0 | 5056 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0049 | 0/0 | 5056 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0050 | 0/0 | 5056 | 2 | 0 | 0 | 0 | 1 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0051 | 0/0 | 5056 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0052 | 0/0 | 5057 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0053 | 0/0 | 5049 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0054 | 0/0 | 5051 | 2 | 0 | 0 | 1 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0055 | 0/0 | 5050 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0056 | 0/0 | 5052 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0057 | 0/0 | 5050 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0058 | 0/0 | 5051 | 2 | 1 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0059 | 0/0 | 5052 | 2 | 1 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0060 | 0/0 | 5050 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0061 | 0/0 | 5050 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0062 | 0/0 | 5050 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0063 | 0/0 | 5050 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0064 | 1/0 | 5050 | 2 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0065 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0066 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0067 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0068 | 0/0 | 5063 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0069 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0070 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0071 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0072 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0073 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0074 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0075 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0076 | 0/0 | 5059 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0077 | 0/0 | 5057 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0078 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0079 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0080 | 0/0 | 5059 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0081 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0082 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0083 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0084 | 0/0 | 5058 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0085 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0086 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0087 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0088 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0089 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0090 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0091 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0092 | 0/0 | 5056 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0093 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0094 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0095 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0096 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0097 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0098 | 0/0 | 5059 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0099 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0100 | 0/0 | 5058 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0101 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0102 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0103 | 0/0 | 5057 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0104 | 0/0 | 5056 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0105 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0106 | 0/0 | 5057 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0107 | 0/0 | 5056 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0108 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0109 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0110 | 0/0 | 5056 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0111 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0112 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0113 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0114 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0115 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0116 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0117 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0118 | 0/0 | 5051 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0119 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0120 | 0/0 | 5051 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0121 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0122 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0123 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0124 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0125 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0126 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0127 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0128 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0129 | 0/0 | 5050 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0130 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0131 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0132 | 0/0 | 5050 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0133 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0134 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0135 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0136 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0137 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0138 | 0/0 | 5051 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0139 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0140 | 0/0 | 5050 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0141 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0142 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0143 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0144 | 0/0 | 5049 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| t0145 | 0/0 | 5058 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4146 | 48 | 5 | 7 | 32 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002 | 0/1 | 4146 | 48 | 1 | 11 | 18 | 3 | 14 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0010 | 0/0 | 4146 | 6 | 0 | 1 | 2 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0020 | 0/0 | 4146 | 3 | 2 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0085 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003 | 0/0 | 4164 | 27 | 1 | 1 | 22 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0014 | 0/0 | 4164 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0049 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0071 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004 | 0/0 | 4146 | 24 | 6 | 1 | 16 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0034 | 1/0 | 4146 | 2 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0045 | 0/0 | 4146 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0067 | 0/0 | 4146 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0068 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005 | 0/0 | 4164 | 15 | 3 | 1 | 11 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0028 | 0/0 | 4164 | 2 | 0 | 0 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0033 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0035 | 0/0 | 4164 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0044 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0048 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0081 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0082 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007 | 0/0 | 4164 | 13 | 5 | 3 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0038 | 0/0 | 4164 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0039 | 0/0 | 4164 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006 | 0/0 | 4146 | 15 | 3 | 3 | 7 | 1 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0086 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0011 | 0/0 | 4146 | 6 | 3 | 2 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0015 | 0/0 | 4146 | 5 | 0 | 1 | 3 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0076 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0077 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0012 | 0/0 | 4161 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0013 | 0/0 | 4161 | 5 | 0 | 2 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0060 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009 | 0/0 | 4146 | 7 | 2 | 3 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0027 | 0/0 | 4146 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0016 | 0/0 | 4143 | 4 | 0 | 0 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0022 | 0/0 | 4143 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0056 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0011c0008 | 0/0 | 4146 | 7 | 0 | 5 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012c0018 | 0/0 | 4146 | 4 | 1 | 2 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012c0041 | 0/0 | 4146 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0040 | 0/0 | 4164 | 2 | 1 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0042 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0089 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0014c0019 | 0/0 | 4149 | 4 | 0 | 0 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0015c0017 | 0/0 | 4164 | 4 | 0 | 2 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0016c0029 | 0/0 | 4149 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0016c0052 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0017c0024 | 0/0 | 4146 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0018c0037 | 0/0 | 4146 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0018c0088 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0019c0023 | 0/0 | 4146 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0020c0025 | 0/0 | 4146 | 3 | 1 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0021c0043 | 0/0 | 4146 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0021c0096 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0022c0026 | 0/0 | 4146 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0023c0021 | 0/0 | 4143 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0024c0031 | 0/0 | 4167 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0025c0030 | 0/0 | 4149 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0026c0053 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0026c0054 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0027c0032 | 0/0 | 4146 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0028c0036 | 0/0 | 4146 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0029c0046 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0029c0047 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0030c0058 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0030c0059 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0031c0097 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0032c0055 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0033c0063 | 0/0 | 4146 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0034c0066 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0035c0065 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0036c0064 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0037c0083 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0038c0084 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0039c0087 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0040c0078 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0041c0069 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0042c0079 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0043c0075 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0044c0074 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0045c0073 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0046c0072 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0047c0080 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0048c0070 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0049c0051 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0050c0050 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0051c0095 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0052c0094 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0053c0093 | 0/0 | 4146 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0054c0091 | 0/0 | 4146 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0055c0090 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0056c0092 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0057c0061 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0058c0062 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0059c0057 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0004 | 0/0 | 9195 | 6 | 0 | 0 | 6 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0006 | 0/0 | 9196 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0007 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0008 | 0/0 | 9197 | 7 | 0 | 1 | 6 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0010 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0011 | 0/0 | 9202 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0012 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0018 | 0/0 | 9196 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0023 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0027 | 0/0 | 9195 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0029 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0042 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0044 | 0/0 | 9203 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0045 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0047 | 0/0 | 9203 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0059 | 0/0 | 9197 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0061 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0062 | 0/0 | 9195 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0070 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0077 | 0/0 | 9202 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0092 | 0/0 | 9201 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0093 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0095 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0097 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0098 | 0/0 | 9204 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0099 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0100 | 0/0 | 9203 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0101 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0113 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0126 | 0/0 | 9197 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0001t0127 | 0/0 | 9197 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0001 | 0/1 | 9201 | 13 | 0 | 3 | 5 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0005 | 0/0 | 9194 | 7 | 1 | 4 | 1 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0016 | 0/0 | 9202 | 5 | 0 | 1 | 3 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0024 | 0/0 | 9202 | 4 | 0 | 0 | 1 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0032 | 0/0 | 9201 | 3 | 0 | 0 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0033 | 0/0 | 9203 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0038 | 0/0 | 9195 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0049 | 0/0 | 9201 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0050 | 0/0 | 9201 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0051 | 0/0 | 9201 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0052 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0072 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0103 | 0/0 | 9202 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0104 | 0/0 | 9201 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0105 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0106 | 0/0 | 9202 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0112 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0002t0145 | 0/0 | 9203 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0010t0001 | 0/0 | 9201 | 4 | 0 | 0 | 2 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0010t0033 | 0/0 | 9203 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0010t0107 | 0/0 | 9201 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0020t0012 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0020t0029 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0020t0041 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0001c0085t0132 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0002 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0003 | 0/0 | 9222 | 11 | 0 | 0 | 11 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0006 | 0/0 | 9214 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0007 | 0/0 | 9221 | 6 | 0 | 0 | 4 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0015 | 0/0 | 9220 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0046 | 0/0 | 9219 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0074 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0078 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0082 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0003t0089 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0014t0006 | 0/0 | 9214 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0014t0015 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0014t0075 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0014t0120 | 0/0 | 9214 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0014t0121 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0049t0087 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0002c0071t0083 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0002 | 0/0 | 9203 | 10 | 1 | 0 | 9 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0003 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0009 | 0/0 | 9203 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0014 | 0/0 | 9197 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0020 | 0/0 | 9202 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0021 | 0/0 | 9202 | 3 | 0 | 0 | 2 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0025 | 0/0 | 9197 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0039 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0040 | 0/0 | 9204 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0004t0081 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0034t0030 | 0/0 | 9200 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0034t0064 | 1/0 | 9195 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0045t0039 | 0/0 | 9203 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0067t0019 | 0/0 | 9204 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0003c0068t0084 | 0/0 | 9203 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0004 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0009 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0010 | 0/0 | 9222 | 4 | 3 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0011 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0012 | 0/0 | 9221 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0027 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0028 | 0/0 | 9215 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0042 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0043 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0005t0135 | 0/0 | 9212 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0028t0020 | 0/0 | 9220 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0028t0080 | 0/0 | 9222 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0033t0023 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0033t0094 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0035t0001 | 0/0 | 9219 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0044t0023 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0048t0029 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0081t0116 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0004c0082t0069 | 0/0 | 9220 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0013 | 0/0 | 9215 | 3 | 1 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0014 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0025 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0055 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0060 | 0/0 | 9213 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0123 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0125 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0129 | 0/0 | 9213 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0136 | 0/0 | 9212 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0007t0137 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0038t0013 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0038t0131 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0005c0039t0017 | 0/0 | 9213 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0002 | 0/0 | 9203 | 3 | 0 | 1 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0003 | 0/0 | 9204 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0004 | 0/0 | 9195 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0009 | 0/0 | 9203 | 3 | 1 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0014 | 0/0 | 9197 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0019 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0022 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0054 | 0/0 | 9196 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0088 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0006t0118 | 0/0 | 9196 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0006c0086t0090 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0011t0010 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0011t0011 | 0/0 | 9202 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0011t0022 | 0/0 | 9204 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0011t0086 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0015t0005 | 0/0 | 9194 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0015t0049 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0015t0050 | 0/0 | 9201 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0015t0115 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0076t0091 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0007c0077t0073 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0012t0013 | 0/0 | 9212 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0012t0017 | 0/0 | 9210 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0013t0004 | 0/0 | 9210 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0013t0006 | 0/0 | 9211 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0013t0014 | 0/0 | 9212 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0013t0058 | 0/0 | 9211 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0013t0124 | 0/0 | 9210 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0008c0060t0139 | 0/0 | 9211 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009t0004 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009t0011 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009t0018 | 0/0 | 9196 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009t0026 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009t0061 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0009t0138 | 0/0 | 9196 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0027t0005 | 0/0 | 9194 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0027t0140 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0009c0027t0144 | 0/0 | 9194 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0016t0005 | 0/0 | 9191 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0016t0038 | 0/0 | 9192 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0016t0141 | 0/0 | 9190 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0016t0142 | 0/0 | 9192 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0022t0004 | 0/0 | 9192 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0022t0008 | 0/0 | 9194 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0022t0062 | 0/0 | 9192 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0010c0056t0143 | 0/0 | 9191 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0011c0008t0004 | 0/0 | 9195 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0011c0008t0027 | 0/0 | 9195 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0011c0008t0034 | 0/0 | 9196 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0011c0008t0036 | 0/0 | 9195 | 3 | 0 | 3 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012c0018t0034 | 0/0 | 9196 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012c0018t0055 | 0/0 | 9195 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012c0018t0056 | 0/0 | 9197 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0012c0041t0035 | 0/0 | 9196 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0040t0028 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0040t0059 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0042t0004 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0042t0134 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0013c0089t0026 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0014c0019t0001 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0014c0019t0052 | 0/0 | 9205 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0014c0019t0102 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0014c0019t0114 | 0/0 | 9205 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0015c0017t0028 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0015c0017t0041 | 0/0 | 9220 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0015c0017t0045 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0015c0017t0096 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0016c0029t0007 | 0/0 | 9206 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0016c0029t0020 | 0/0 | 9205 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0016c0052t0020 | 0/0 | 9205 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0017c0024t0037 | 0/0 | 9197 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0018c0037t0063 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0018c0037t0109 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0018c0088t0010 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0019c0023t0031 | 0/0 | 9202 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0020c0025t0025 | 0/0 | 9197 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0020c0025t0130 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0021c0043t0063 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0021c0043t0064 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0021c0096t0006 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0022c0026t0053 | 0/0 | 9194 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0022c0026t0117 | 0/0 | 9194 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0023c0021t0006 | 0/0 | 9193 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0023c0021t0054 | 0/0 | 9193 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0024c0031t0012 | 0/0 | 9224 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0024c0031t0043 | 0/0 | 9225 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0025c0030t0048 | 0/0 | 9204 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0026c0053t0001 | 0/0 | 9222 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0026c0054t0110 | 0/0 | 9222 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0027c0032t0026 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0027c0032t0065 | 0/0 | 9211 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0028c0036t0030 | 0/0 | 9200 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0029c0046t0019 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0029c0047t0108 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0030c0058t0057 | 0/0 | 9192 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0030c0059t0058 | 0/0 | 9193 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0031c0097t0015 | 0/0 | 9223 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0032c0055t0002 | 0/0 | 9224 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0033c0063t0005 | 0/0 | 9194 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0034c0066t0068 | 0/0 | 9208 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0035c0065t0066 | 0/0 | 9210 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0036c0064t0067 | 0/0 | 9211 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0037c0083t0046 | 0/0 | 9219 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0038c0084t0019 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0039c0087t0021 | 0/0 | 9220 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0040c0078t0015 | 0/0 | 9220 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0041c0069t0111 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0042c0079t0079 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0043c0075t0076 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0044c0074t0071 | 0/0 | 9219 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0045c0073t0056 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0046c0072t0026 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0047c0080t0085 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0048c0070t0012 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0049c0051t0023 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0050c0050t0022 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0051c0095t0057 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0052c0094t0004 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0053c0093t0014 | 0/0 | 9197 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0054c0091t0122 | 0/0 | 9197 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0055c0090t0119 | 0/0 | 9197 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0056c0092t0133 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0057c0061t0035 | 0/0 | 9193 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0058c0062t0014 | 0/0 | 9194 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| a0059c0057t0128 | 0/0 | 9192 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | copy fasta | chr3 | 124960710 | 125060997 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0018g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0018g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0018g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0023g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0027g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0029g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0042g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0044g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0044g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0045g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0047g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0047g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0059g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0061g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0062g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0070g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0077g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0092g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0093g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0095g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0097g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0098g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0099g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0100g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0101g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0113g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0126g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0001t0127g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0016g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0016g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0016g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0024g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0024g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0024g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0024g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0032g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0032g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0032g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0033g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0033g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0038g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0038g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0049g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0050g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0051g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0051g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0052g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0072g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0103g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0104g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0105g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0106g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0112g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0002t0145g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0010t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0010t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0010t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0010t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0010t0033g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0010t0107g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0020t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0020t0029g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0020t0041g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0001c0085t0132g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0006g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0015g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0015g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0046g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0074g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0078g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0082g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0003t0089g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0014t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0014t0015g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0014t0075g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0014t0120g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0014t0121g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0049t0087g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0002c0071t0083g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0020g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0021g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0021g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0021g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0025g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0039g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0040g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0040g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0004t0081g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0034t0030g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0034t0064g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0045t0039g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0067t0019g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0003c0068t0084g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0010g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0012g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0027g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0028g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0028g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0042g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0043g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0005t0135g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0028t0020g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0028t0080g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0033t0023g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0033t0094g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0035t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0035t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0044t0023g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0048t0029g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0081t0116g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0004c0082t0069g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0013g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0013g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0013g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0014g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0025g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0055g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0060g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0060g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0123g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0125g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0129g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0136g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0007t0137g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0038t0013g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0038t0131g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0039t0017g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0005c0039t0017g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0009g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0009g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0014g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0019g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0022g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0054g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0088g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0006t0118g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0006c0086t0090g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0011t0010g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0011t0011g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0011t0011g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0011t0022g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0011t0086g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0015t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0015t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0015t0049g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0015t0050g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0015t0115g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0076t0091g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0007c0077t0073g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0012t0013g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0012t0013g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0012t0017g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0012t0017g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0013t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0013t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0013t0014g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0013t0058g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0013t0124g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0008c0060t0139g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0018g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0018g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0026g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0061g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0009t0138g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0027t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0027t0140g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0009c0027t0144g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0016t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0016t0038g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0016t0141g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0016t0142g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0022t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0022t0008g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0022t0062g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0010c0056t0143g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0027g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0027g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0034g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0036g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0036g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0011c0008t0036g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0012c0018t0034g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0012c0018t0034g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0012c0018t0055g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0012c0018t0056g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0012c0041t0035g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0012c0041t0035g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0013c0040t0028g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0013c0040t0059g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0013c0042t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0013c0042t0134g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0013c0089t0026g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0014c0019t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0014c0019t0052g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0014c0019t0102g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0014c0019t0114g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0015c0017t0028g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0015c0017t0041g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0015c0017t0045g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0015c0017t0096g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0016c0029t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0016c0029t0020g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0016c0052t0020g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0017c0024t0037g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0017c0024t0037g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0018c0037t0063g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0018c0037t0109g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0018c0088t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0019c0023t0031g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0019c0023t0031g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0019c0023t0031g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0020c0025t0025g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0020c0025t0130g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0021c0043t0063g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0021c0043t0064g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0021c0096t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0022c0026t0053g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0022c0026t0053g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0022c0026t0117g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0023c0021t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0023c0021t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0023c0021t0054g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0024c0031t0012g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0024c0031t0043g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0025c0030t0048g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0025c0030t0048g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0026c0053t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0026c0054t0110g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0027c0032t0026g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0027c0032t0065g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0028c0036t0030g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0028c0036t0030g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0029c0046t0019g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0029c0047t0108g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0030c0058t0057g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0030c0059t0058g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0031c0097t0015g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0032c0055t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0033c0063t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0034c0066t0068g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0035c0065t0066g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0036c0064t0067g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0037c0083t0046g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0038c0084t0019g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0039c0087t0021g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0040c0078t0015g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0041c0069t0111g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0042c0079t0079g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0043c0075t0076g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0044c0074t0071g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0045c0073t0056g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0046c0072t0026g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0047c0080t0085g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0048c0070t0012g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0049c0051t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0050c0050t0022g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0051c0095t0057g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0052c0094t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0053c0093t0014g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0054c0091t0122g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0055c0090t0119g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0056c0092t0133g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0057c0061t0035g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0058c0062t0014g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| a0059c0057t0128g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0039 | c0087 | t0021 | g0090 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00099 | hp2 | a0001 | c0002 | t0051 | g0136 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00140 | hp1 | a0001 | c0002 | t0106 | g0094 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00140 | hp2 | a0003 | c0004 | t0021 | g0134 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00323 | hp1 | a0006 | c0006 | t0054 | g0249 | EUR | FIN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00323 | hp2 | a0024 | c0031 | t0012 | g0032 | EUR | FIN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00438 | hp1 | a0003 | c0004 | t0002 | g0056 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00544 | hp1 | a0007 | c0015 | t0049 | g0058 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00544 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00558 | hp1 | a0008 | c0013 | t0058 | g0230 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00558 | hp2 | a0010 | c0056 | t0143 | g0210 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00597 | hp1 | a0007 | c0015 | t0005 | g0287 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00597 | hp2 | a0005 | c0007 | t0060 | g0335 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00609 | hp1 | a0001 | c0001 | t0006 | g0282 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00609 | hp2 | a0003 | c0004 | t0003 | g0104 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00621 | hp1 | a0004 | c0048 | t0029 | g0023 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00621 | hp2 | a0004 | c0005 | t0043 | g0147 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00639 | hp1 | a0055 | c0090 | t0119 | g0350 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00639 | hp2 | a0001 | c0020 | t0029 | g0014 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00642 | hp1 | a0007 | c0011 | t0011 | g0124 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00642 | hp2 | a0001 | c0002 | t0005 | g0292 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0126 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00733 | hp1 | a0006 | c0006 | t0118 | g0297 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00733 | hp2 | a0011 | c0008 | t0027 | g0236 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00735 | hp1 | a0006 | c0006 | t0002 | g0178 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00735 | hp2 | a0020 | c0025 | t0025 | g0008 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00738 | hp1 | a0003 | c0068 | t0084 | g0196 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00738 | hp2 | a0011 | c0008 | t0036 | g0240 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00741 | hp1 | a0012 | c0018 | t0034 | g0329 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG00741 | hp2 | a0011 | c0008 | t0034 | g0235 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01071 | hp1 | a0007 | c0015 | t0005 | g0269 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01071 | hp2 | a0009 | c0009 | t0061 | g0321 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01074 | hp2 | a0020 | c0025 | t0025 | g0008 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01081 | hp1 | a0001 | c0002 | t0049 | g0054 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01081 | hp2 | a0010 | c0022 | t0008 | g0233 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01099 | hp1 | a0009 | c0009 | t0004 | g0330 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01099 | hp2 | a0001 | c0002 | t0016 | g0151 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01106 | hp1 | a0001 | c0001 | t0061 | g0290 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01106 | hp2 | a0006 | c0006 | t0009 | g0141 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01109 | hp1 | a0007 | c0011 | t0010 | g0191 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01109 | hp2 | a0004 | c0005 | t0010 | g0165 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01167 | hp1 | a0001 | c0002 | t0104 | g0179 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01167 | hp2 | a0012 | c0041 | t0035 | g0312 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01168 | hp1 | a0011 | c0008 | t0036 | g0242 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01168 | hp2 | a0001 | c0002 | t0005 | g0293 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01169 | hp1 | a0011 | c0008 | t0036 | g0241 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01169 | hp2 | a0012 | c0041 | t0035 | g0310 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01192 | hp1 | a0001 | c0001 | t0127 | g0301 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01192 | hp2 | a0001 | c0085 | t0132 | g0289 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01243 | hp1 | a0005 | c0007 | t0013 | g0307 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01243 | hp2 | a0001 | c0001 | t0100 | g0095 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01255 | hp1 | a0043 | c0075 | t0076 | g0181 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01255 | hp2 | a0015 | c0017 | t0028 | g0284 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01256 | hp1 | a0001 | c0002 | t0051 | g0137 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01256 | hp2 | a0009 | c0009 | t0138 | g0348 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0302 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01261 | hp2 | a0012 | c0018 | t0034 | g0323 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01346 | hp1 | a0005 | c0007 | t0129 | g0347 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01346 | hp2 | a0004 | c0035 | t0001 | g0154 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01358 | hp2 | a0001 | c0001 | t0044 | g0103 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01361 | hp1 | a0024 | c0031 | t0043 | g0038 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01361 | hp2 | a0009 | c0027 | t0144 | g0328 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01433 | hp1 | a0010 | c0022 | t0004 | g0232 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01433 | hp2 | a0016 | c0029 | t0007 | g0035 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01496 | hp1 | a0009 | c0027 | t0140 | g0331 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01496 | hp2 | a0005 | c0007 | t0014 | g0309 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01517 | hp1 | a0025 | c0030 | t0048 | g0036 | EUR | IBS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01517 | hp2 | a0012 | c0018 | t0055 | g0320 | EUR | IBS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01884 | hp1 | a0005 | c0007 | t0013 | g0314 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0081 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01891 | hp1 | a0004 | c0081 | t0116 | g0246 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01891 | hp2 | a0047 | c0080 | t0085 | g0086 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01928 | hp1 | a0008 | c0013 | t0014 | g0213 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01975 | hp1 | a0026 | c0053 | t0001 | g0033 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01975 | hp2 | a0005 | c0039 | t0017 | g0325 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01981 | hp1 | a0003 | c0004 | t0020 | g0062 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG01981 | hp2 | a0008 | c0013 | t0006 | g0229 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02004 | hp1 | a0032 | c0055 | t0002 | g0040 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02004 | hp2 | a0002 | c0003 | t0006 | g0286 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02027 | hp1 | a0003 | c0004 | t0002 | g0170 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02027 | hp2 | a0006 | c0006 | t0019 | g0110 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02055 | hp1 | a0027 | c0032 | t0065 | g0011 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02055 | hp2 | a0018 | c0037 | t0063 | g0256 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02056 | hp1 | a0001 | c0002 | t0038 | g0252 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02056 | hp2 | a0006 | c0006 | t0003 | g0111 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02074 | hp1 | a0001 | c0001 | t0099 | g0140 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02074 | hp2 | a0002 | c0003 | t0015 | g0071 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02080 | hp1 | a0002 | c0003 | t0007 | g0100 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02080 | hp2 | a0001 | c0001 | t0018 | g0254 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02083 | hp1 | a0005 | c0007 | t0136 | g0319 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02083 | hp2 | a0010 | c0016 | t0005 | g0222 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02132 | hp1 | a0053 | c0093 | t0014 | g0327 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02132 | hp2 | a0028 | c0036 | t0030 | g0067 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02135 | hp1 | a0005 | c0038 | t0131 | g0303 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02135 | hp2 | a0001 | c0002 | t0038 | g0245 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02148 | hp1 | a0001 | c0001 | t0059 | g0262 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02148 | hp2 | a0001 | c0002 | t0005 | g0255 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02155 | hp1 | a0006 | c0006 | t0014 | g0270 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02155 | hp2 | a0005 | c0007 | t0060 | g0334 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02165 | hp1 | a0001 | c0001 | t0042 | g0097 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02165 | hp2 | a0006 | c0006 | t0009 | g0047 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02257 | hp1 | a0036 | c0064 | t0067 | g0009 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02257 | hp2 | a0022 | c0026 | t0117 | g0306 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02258 | hp1 | a0030 | c0058 | t0057 | g0220 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02258 | hp2 | a0018 | c0088 | t0010 | g0177 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02273 | hp1 | a0015 | c0017 | t0041 | g0152 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02273 | hp2 | a0001 | c0001 | t0029 | g0153 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02280 | hp1 | a0009 | c0009 | t0011 | g0204 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02280 | hp2 | a0006 | c0086 | t0090 | g0084 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0244 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02293 | hp2 | a0001 | c0010 | t0033 | g0019 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02300 | hp1 | a0026 | c0054 | t0110 | g0039 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02300 | hp2 | a0016 | c0052 | t0020 | g0041 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02451 | hp1 | a0046 | c0072 | t0026 | g0271 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02451 | hp2 | a0005 | c0007 | t0123 | g0351 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02523 | hp1 | a0004 | c0005 | t0135 | g0272 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02572 | hp1 | a0029 | c0046 | t0019 | g0029 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02572 | hp2 | a0007 | c0077 | t0073 | g0087 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02602 | hp1 | a0004 | c0028 | t0020 | g0025 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02602 | hp2 | a0001 | c0002 | t0016 | g0061 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02615 | hp1 | a0034 | c0066 | t0068 | g0010 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02615 | hp2 | a0003 | c0004 | t0014 | g0285 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02622 | hp1 | a0001 | c0020 | t0012 | g0016 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02622 | hp2 | a0013 | c0042 | t0134 | g0345 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02630 | hp1 | a0041 | c0069 | t0111 | g0203 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02630 | hp2 | a0050 | c0050 | t0022 | g0031 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02647 | hp1 | a0003 | c0004 | t0002 | g0089 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02647 | hp2 | a0042 | c0079 | t0079 | g0180 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02698 | hp1 | a0001 | c0010 | t0001 | g0030 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02698 | hp2 | a0001 | c0001 | t0126 | g0274 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02717 | hp1 | a0005 | c0007 | t0055 | g0322 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02717 | hp2 | a0029 | c0047 | t0108 | g0018 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02723 | hp1 | a0012 | c0018 | t0056 | g0352 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02723 | hp2 | a0027 | c0032 | t0026 | g0243 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02735 | hp1 | a0001 | c0002 | t0024 | g0138 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02735 | hp2 | a0003 | c0045 | t0039 | g0026 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02738 | hp1 | a0001 | c0001 | t0098 | g0188 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02738 | hp2 | a0001 | c0001 | t0077 | g0043 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02809 | hp1 | a0002 | c0003 | t0082 | g0184 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02809 | hp2 | a0008 | c0060 | t0139 | g0218 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02818 | hp1 | a0030 | c0059 | t0058 | g0221 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02818 | hp2 | a0051 | c0095 | t0057 | g0317 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02886 | hp1 | a0020 | c0025 | t0130 | g0318 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02886 | hp2 | a0004 | c0005 | t0010 | g0066 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02895 | hp1 | a0035 | c0065 | t0066 | g0012 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02895 | hp2 | a0004 | c0005 | t0010 | g0044 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02965 | hp1 | a0007 | c0011 | t0022 | g0002 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02965 | hp2 | a0049 | c0051 | t0023 | g0021 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02970 | hp1 | a0001 | c0020 | t0041 | g0017 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02970 | hp2 | a0054 | c0091 | t0122 | g0311 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03041 | hp1 | a0021 | c0043 | t0063 | g0342 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03041 | hp2 | a0001 | c0001 | t0092 | g0187 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03098 | hp1 | a0019 | c0023 | t0031 | g0193 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03098 | hp2 | a0006 | c0006 | t0022 | g0088 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03139 | hp1 | a0007 | c0011 | t0022 | g0002 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03139 | hp2 | a0056 | c0092 | t0133 | g0316 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03195 | hp1 | a0003 | c0004 | t0081 | g0176 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03195 | hp2 | a0004 | c0033 | t0023 | g0163 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03209 | hp1 | a0019 | c0023 | t0031 | g0192 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03209 | hp2 | a0013 | c0042 | t0004 | g0349 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03239 | hp2 | a0003 | c0034 | t0030 | g0114 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03453 | hp1 | a0004 | c0082 | t0069 | g0190 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03486 | hp1 | a0009 | c0009 | t0026 | g0344 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03486 | hp2 | a0007 | c0011 | t0086 | g0080 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03490 | hp1 | a0001 | c0002 | t0032 | g0200 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0300 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03491 | hp1 | a0011 | c0008 | t0027 | g0237 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03491 | hp2 | a0001 | c0002 | t0024 | g0092 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03492 | hp1 | a0001 | c0002 | t0024 | g0093 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03492 | hp2 | a0001 | c0002 | t0032 | g0199 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03516 | hp1 | a0019 | c0023 | t0031 | g0182 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03516 | hp2 | a0003 | c0004 | t0040 | g0174 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03540 | hp1 | a0005 | c0007 | t0025 | g0308 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03540 | hp2 | a0021 | c0043 | t0064 | g0341 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03579 | hp1 | a0045 | c0073 | t0056 | g0299 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03579 | hp2 | a0003 | c0004 | t0040 | g0175 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03654 | hp1 | a0006 | c0006 | t0004 | g0291 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03654 | hp2 | a0002 | c0003 | t0007 | g0082 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03710 | hp1 | a0001 | c0002 | t0103 | g0159 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03710 | hp2 | a0033 | c0063 | t0005 | g0239 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03831 | hp1 | a0003 | c0067 | t0019 | g0063 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03831 | hp2 | a0002 | c0003 | t0006 | g0267 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03834 | hp1 | a0001 | c0002 | t0032 | g0201 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03834 | hp2 | a0011 | c0008 | t0004 | g0238 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03927 | hp1 | a0007 | c0015 | t0050 | g0064 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03927 | hp2 | a0040 | c0078 | t0015 | g0155 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04115 | hp1 | a0001 | c0010 | t0001 | g0024 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04115 | hp2 | a0001 | c0001 | t0044 | g0160 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04184 | hp2 | a0007 | c0011 | t0011 | g0060 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04199 | hp1 | a0001 | c0002 | t0145 | g0353 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04199 | hp2 | a0004 | c0028 | t0080 | g0027 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04228 | hp1 | a0001 | c0010 | t0107 | g0020 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG04228 | hp2 | a0002 | c0003 | t0007 | g0148 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18612 | hp1 | a0001 | c0002 | t0016 | g0145 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18612 | hp2 | a0009 | c0009 | t0018 | g0339 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18747 | hp1 | a0004 | c0005 | t0012 | g0157 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18747 | hp2 | a0001 | c0002 | t0005 | g0288 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18906 | hp1 | a0004 | c0044 | t0023 | g0015 | AFR | YRI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18906 | hp2 | a0001 | c0001 | t0070 | g0194 | AFR | YRI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18939 | hp1 | a0001 | c0001 | t0018 | g0253 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18939 | hp2 | a0015 | c0017 | t0045 | g0131 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0068 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18940 | hp2 | a0008 | c0012 | t0017 | g0006 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18941 | hp1 | a0001 | c0001 | t0045 | g0128 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18942 | hp1 | a0001 | c0001 | t0047 | g0123 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18944 | hp1 | a0017 | c0024 | t0037 | g0007 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18944 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18945 | hp1 | a0003 | c0004 | t0021 | g0057 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18945 | hp2 | a0006 | c0006 | t0002 | g0098 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18946 | hp1 | a0002 | c0003 | t0015 | g0083 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0294 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18948 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18948 | hp2 | a0001 | c0010 | t0001 | g0013 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18950 | hp1 | a0009 | c0027 | t0005 | g0333 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18950 | hp2 | a0002 | c0003 | t0007 | g0070 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18951 | hp1 | a0004 | c0005 | t0011 | g0197 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18951 | hp2 | a0003 | c0004 | t0009 | g0195 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18952 | hp1 | a0052 | c0094 | t0004 | g0332 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18952 | hp2 | a0002 | c0003 | t0007 | g0069 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18953 | hp1 | a0028 | c0036 | t0030 | g0119 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18953 | hp2 | a0001 | c0001 | t0027 | g0281 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18957 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18959 | hp1 | a0007 | c0015 | t0115 | g0055 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18959 | hp2 | a0001 | c0001 | t0012 | g0172 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18960 | hp1 | a0005 | c0007 | t0137 | g0337 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18966 | hp1 | a0014 | c0019 | t0114 | g0205 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0113 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18967 | hp2 | a0003 | c0004 | t0002 | g0167 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18968 | hp1 | a0002 | c0014 | t0015 | g0116 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18968 | hp2 | a0001 | c0002 | t0112 | g0149 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18970 | hp1 | a0010 | c0016 | t0038 | g0219 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18970 | hp2 | a0004 | c0005 | t0004 | g0278 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18973 | hp1 | a0005 | c0007 | t0013 | g0338 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18973 | hp2 | a0017 | c0024 | t0037 | g0007 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18974 | hp1 | a0003 | c0004 | t0009 | g0049 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18974 | hp2 | a0002 | c0003 | t0089 | g0125 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18975 | hp1 | a0001 | c0002 | t0052 | g0135 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0106 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18977 | hp1 | a0004 | c0035 | t0001 | g0102 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18977 | hp2 | a0001 | c0001 | t0062 | g0280 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18982 | hp1 | a0003 | c0004 | t0002 | g0169 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18983 | hp1 | a0001 | c0001 | t0113 | g0150 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18983 | hp2 | a0002 | c0003 | t0002 | g0156 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18986 | hp1 | a0017 | c0024 | t0037 | g0265 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18986 | hp2 | a0058 | c0062 | t0014 | g0214 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18988 | hp1 | a0031 | c0097 | t0015 | g0207 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18988 | hp2 | a0003 | c0004 | t0009 | g0072 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18989 | hp1 | a0001 | c0002 | t0033 | g0050 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18990 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18990 | hp2 | a0002 | c0003 | t0078 | g0073 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18991 | hp1 | a0037 | c0083 | t0046 | g0118 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18991 | hp2 | a0008 | c0013 | t0124 | g0234 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18993 | hp1 | a0014 | c0019 | t0052 | g0208 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18993 | hp2 | a0044 | c0074 | t0071 | g0189 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0099 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18994 | hp2 | a0001 | c0001 | t0095 | g0101 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18995 | hp2 | a0002 | c0003 | t0003 | g0173 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18997 | hp1 | a0002 | c0049 | t0087 | g0028 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18997 | hp2 | a0005 | c0038 | t0013 | g0324 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18998 | hp1 | a0023 | c0021 | t0006 | g0216 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18998 | hp2 | a0009 | c0009 | t0018 | g0326 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18999 | hp1 | a0008 | c0012 | t0013 | g0228 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18999 | hp2 | a0004 | c0005 | t0028 | g0259 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19000 | hp1 | a0023 | c0021 | t0054 | g0215 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19000 | hp2 | a0001 | c0002 | t0016 | g0046 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19001 | hp1 | a0013 | c0040 | t0028 | g0336 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19001 | hp2 | a0003 | c0004 | t0002 | g0166 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19002 | hp1 | a0010 | c0016 | t0142 | g0225 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19002 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19003 | hp1 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19003 | hp2 | a0005 | c0039 | t0017 | g0340 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19009 | hp1 | a0001 | c0001 | t0008 | g0268 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19009 | hp2 | a0008 | c0012 | t0013 | g0227 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19010 | hp2 | a0002 | c0003 | t0046 | g0117 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19012 | hp2 | a0002 | c0014 | t0121 | g0257 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19030 | hp1 | a0021 | c0096 | t0006 | g0343 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19030 | hp2 | a0013 | c0089 | t0026 | g0313 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19043 | hp1 | a0002 | c0071 | t0083 | g0185 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19043 | hp2 | a0059 | c0057 | t0128 | g0211 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19054 | hp1 | a0002 | c0003 | t0074 | g0075 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19054 | hp2 | a0010 | c0022 | t0062 | g0231 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19055 | hp2 | a0008 | c0012 | t0017 | g0226 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19056 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19056 | hp2 | a0001 | c0001 | t0101 | g0121 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19057 | hp1 | a0008 | c0012 | t0017 | g0006 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19057 | hp2 | a0001 | c0002 | t0016 | g0051 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19060 | hp1 | a0048 | c0070 | t0012 | g0052 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19060 | hp2 | a0014 | c0019 | t0001 | g0209 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19062 | hp1 | a0004 | c0005 | t0028 | g0261 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19062 | hp2 | a0023 | c0021 | t0006 | g0217 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19063 | hp1 | a0001 | c0001 | t0018 | g0251 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19063 | hp2 | a0003 | c0004 | t0002 | g0171 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19064 | hp1 | a0001 | c0001 | t0008 | g0266 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19064 | hp2 | a0001 | c0002 | t0072 | g0133 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19067 | hp1 | a0002 | c0014 | t0006 | g0258 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19067 | hp2 | a0014 | c0019 | t0102 | g0206 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19068 | hp1 | a0002 | c0014 | t0120 | g0263 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19068 | hp2 | a0004 | c0005 | t0042 | g0158 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19070 | hp1 | a0003 | c0004 | t0025 | g0273 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19070 | hp2 | a0001 | c0010 | t0001 | g0022 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19076 | hp1 | a0001 | c0002 | t0024 | g0115 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19078 | hp1 | a0006 | c0006 | t0003 | g0109 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19078 | hp2 | a0015 | c0017 | t0096 | g0048 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19079 | hp1 | a0001 | c0002 | t0033 | g0045 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19079 | hp2 | a0001 | c0001 | t0047 | g0122 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19082 | hp1 | a0004 | c0005 | t0027 | g0260 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19082 | hp2 | a0001 | c0002 | t0105 | g0139 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19084 | hp1 | a0002 | c0014 | t0075 | g0078 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19084 | hp2 | a0003 | c0004 | t0021 | g0168 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19086 | hp1 | a0002 | c0003 | t0003 | g0105 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19086 | hp2 | a0001 | c0001 | t0097 | g0144 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19088 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19088 | hp2 | a0004 | c0005 | t0012 | g0112 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19090 | hp1 | a0002 | c0003 | t0007 | g0076 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19090 | hp2 | a0008 | c0013 | t0004 | g0212 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19091 | hp1 | a0001 | c0001 | t0023 | g0059 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA19091 | hp2 | a0006 | c0006 | t0002 | g0108 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA20129 | hp1 | a0006 | c0006 | t0088 | g0065 | AFR | ASW | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA20129 | hp2 | a0001 | c0001 | t0093 | g0162 | AFR | ASW | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA20752 | hp1 | a0001 | c0002 | t0050 | g0198 | EUR | TSI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA20752 | hp2 | a0016 | c0029 | t0020 | g0034 | EUR | TSI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02109 | hp1 | a0018 | c0037 | t0109 | g0186 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02109 | hp2 | a0022 | c0026 | t0053 | g0305 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02486 | hp1 | a0013 | c0040 | t0059 | g0315 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02486 | hp2 | a0057 | c0061 | t0035 | g0223 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0298 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG02559 | hp2 | a0005 | c0007 | t0125 | g0346 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03471 | hp1 | a0022 | c0026 | t0053 | g0304 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG03471 | hp2 | a0038 | c0084 | t0019 | g0085 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG06807 | hp1 | a0025 | c0030 | t0048 | g0037 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| HG06807 | hp2 | a0004 | c0033 | t0094 | g0164 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18955 | hp1 | a0004 | c0005 | t0009 | g0077 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA18955 | hp2 | a0010 | c0016 | t0141 | g0224 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA20300 | hp1 | a0004 | c0005 | t0010 | g0202 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA20300 | hp2 | a0006 | c0006 | t0009 | g0042 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA21309 | hp1 | a0007 | c0076 | t0091 | g0161 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| NA21309 | hp2 | a0003 | c0004 | t0039 | g0053 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0127 | REF | REF | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| homoSapiens_grch38 | hp1 | a0003 | c0034 | t0064 | g0264 | REF | REF | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:124970801
|
G | T | 1 | a0045 | 1 | HG03579.hp1 | missense_variant&splice_region_variant | MODERATE | c.3997C>A | p.Pro1333Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4104/9195 | 3997/4146 | 1333/1381 | chr3 | 124970801 | ||
| chr3:124973819
|
C | T | 1 | a0041 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.3908G>A | p.Arg1303His | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/17 | 4015/9195 | 3908/4146 | 1303/1381 | chr3 | 124973819 | ||
| chr3:124997805
|
C | T | 1 | a0054 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3536G>A | p.Arg1179Gln | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/17 | 3643/9195 | 3536/4146 | 1179/1381 | chr3 | 124997805 | ||
| chr3:125005330
|
A | C | 1 | a0050 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.3232T>G | p.Phe1078Val | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/17 | 3339/9195 | 3232/4146 | 1078/1381 | chr3 | 125005330 | ||
| chr3:125009743
|
G | A | 1 | a0044 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.3155C>T | p.Pro1052Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/17 | 3262/9195 | 3155/4146 | 1052/1381 | chr3 | 125009743 | ||
| chr3:125009782
|
A | G | 29 | a0001a0004a0007others(26): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
missense_variant | MODERATE | c.3116T>C | p.Met1039Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/17 | 3223/9195 | 3116/4146 | 1039/1381 | chr3 | 125009782 | ||
| chr3:125012641
|
C | G | 42 | a0001a0002a0004others(39): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
missense_variant | MODERATE | c.2938G>C | p.Val980Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 3045/9195 | 2938/4146 | 980/1381 | chr3 | 125012641 | ||
| chr3:125012709
|
G | A | 4 | a0029a0030a0034others(1): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.2870C>T | p.Thr957Met | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2977/9195 | 2870/4146 | 957/1381 | chr3 | 125012709 | ||
| chr3:125012845
|
T | A | 23 | a0002a0004a0005others(20): Show | 119 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(116): Show |
missense_variant | MODERATE | c.2734A>T | p.Thr912Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2841/9195 | 2734/4146 | 912/1381 | chr3 | 125012845 | ||
| chr3:125012956
|
T | A | 1 | a0028 | 2 | HG02132.hp2 NA18953.hp1 |
missense_variant | MODERATE | c.2623A>T | p.Thr875Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2730/9195 | 2623/4146 | 875/1381 | chr3 | 125012956 | ||
| chr3:125013258
|
T | C | 3 | a0020a0043a0055 | 5 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
missense_variant | MODERATE | c.2321A>G | p.Gln774Arg | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2428/9195 | 2321/4146 | 774/1381 | chr3 | 125013258 | ||
| chr3:125013351
|
G | A | 1 | a0019 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.2228C>T | p.Ser743Phe | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2335/9195 | 2228/4146 | 743/1381 | chr3 | 125013351 | ||
| chr3:125013490
|
C | T | 3 | a0020a0043a0055 | 5 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
missense_variant | MODERATE | c.2089G>A | p.Ala697Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2196/9195 | 2089/4146 | 697/1381 | chr3 | 125013490 | ||
| chr3:125013575
|
A | AGAGGAGG others(11): Show |
19 | a0002a0004a0005others(16): Show | 111 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(108): Show |
disruptive_inframe_insertion | MODERATE | c.1986_2003dupCTCTTC others(12): Show |
p.Ser663_Ser668dup | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2110/9195 | 2003/4146 | 668/1381 | chr3 | 125013575 | ||
| chr3:125013582
|
G | A | 6 | a0019a0029a0030others(3): Show | 10 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
missense_variant | MODERATE | c.1997C>T | p.Ser666Phe | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2104/9195 | 1997/4146 | 666/1381 | chr3 | 125013582 | ||
| chr3:125013651
|
G | A | 1 | a0020 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1928C>T | p.Pro643Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2035/9195 | 1928/4146 | 643/1381 | chr3 | 125013651 | ||
| chr3:125013774
|
A | G | 16 | a0001a0006a0009others(13): Show | 160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): Show |
missense_variant | MODERATE | c.1805T>C | p.Phe602Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 1912/9195 | 1805/4146 | 602/1381 | chr3 | 125013774 | ||
| chr3:125013895
|
T | A | 4 | a0029a0030a0034others(1): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.1684A>T | p.Thr562Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 1791/9195 | 1684/4146 | 562/1381 | chr3 | 125013895 | ||
| chr3:125013976
|
A | G | 1 | a0017 | 3 | NA18944.hp1 NA18973.hp2 NA18986.hp1 |
missense_variant | MODERATE | c.1603T>C | p.Tyr535His | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 1710/9195 | 1603/4146 | 535/1381 | chr3 | 125013976 | ||
| chr3:125019409
|
T | C | 1 | a0040 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1441A>G | p.Asn481Asp | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/17 | 1548/9195 | 1441/4146 | 481/1381 | chr3 | 125019409 | ||
| chr3:125027205
|
A | G | 24 | a0001a0006a0009others(21): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
missense_variant&splice_region_variant | MODERATE | c.913T>C | p.Ser305Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 1020/9195 | 913/4146 | 305/1381 | chr3 | 125027205 | ||
| chr3:125027397
|
C | G | 1 | a0019 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.721G>C | p.Gly241Arg | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 828/9195 | 721/4146 | 241/1381 | chr3 | 125027397 | ||
| chr3:125027504
|
G | A | 1 | a0037 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.614C>T | p.Ser205Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 721/9195 | 614/4146 | 205/1381 | chr3 | 125027504 | ||
| chr3:125029285
|
C | T | 2 | a0049a0050 | 2 | HG02630.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.520G>A | p.Gly174Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/17 | 627/9195 | 520/4146 | 174/1381 | chr3 | 125029285 | ||
| chr3:125055588
|
T | G | 15 | a0005a0009a0011others(12): Show | 61 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
missense_variant | MODERATE | c.303A>C | p.Arg101Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 410/9195 | 303/4146 | 101/1381 | chr3 | 125055588 | ||
| chr3:125055718
|
C | T | 4 | a0027a0034a0035others(1): Show | 5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
missense_variant | MODERATE | c.173G>A | p.Arg58His | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 280/9195 | 173/4146 | 58/1381 | chr3 | 125055718 | ||
| chr3:125055799
|
C | T | 2 | a0011a0033 | 8 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
missense_variant | MODERATE | c.92G>A | p.Arg31Gln | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 199/9195 | 92/4146 | 31/1381 | chr3 | 125055799 | ||
| chr3:125055810
|
GGCC | G | 7 | a0008a0010a0023others(4): Show | 27 | HG00558.hp1 HG00558.hp2 HG01081.hp2 others(24): Show |
disruptive_inframe_deletion | MODERATE | c.78_80delGGC | p.Ala27del | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 187/9195 | 78/4146 | 26/1381 | chr3 | 125055810 | ||
| chr3:125055820
|
G | GGCA | 2 | a0014a0031 | 5 | NA18966.hp1 NA18988.hp1 NA18993.hp1 others(2): Show |
conservative_inframe_insertion | MODERATE | c.68_70dupTGC | p.Leu23dup | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 177/9195 | 70/4146 | 24/1381 | chr3 | 125055820 | ||
| chr3:125055821
|
G | GCAT | 5 | a0016a0024a0025others(2): Show | 10 | HG00323.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
conservative_inframe_insertion | MODERATE | c.69_70insATG | p.Leu23_Pro24insMet | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 176/9195 | 69/4146 | 23/1381 | chr3 | 125055821 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:124970766
|
G | A | 1 | a0004c0082 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.4032C>T | p.Asn1344Asn | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4139/9195 | 4032/4146 | 1344/1381 | chr3 | 124970766 | ||
| chr3:124973845
|
C | T | 73 | a0001c0001a0001c0020a0001c0085others(70): Show | 266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
synonymous_variant | LOW | c.3882G>A | p.Pro1294Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/17 | 3989/9195 | 3882/4146 | 1294/1381 | chr3 | 124973845 | ||
| chr3:124977894
|
G | A | 1 | a0004c0048 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.3786C>T | p.Leu1262Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/17 | 3893/9195 | 3786/4146 | 1262/1381 | chr3 | 124977894 | ||
| chr3:125001880
|
G | A | 1 | a0003c0067 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.3489C>T | p.Leu1163Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/17 | 3596/9195 | 3489/4146 | 1163/1381 | chr3 | 125001880 | ||
| chr3:125009742
|
C | T | 3 | a0026c0053a0043c0075a0055c0090 | 3 | HG00639.hp1 HG01255.hp1 HG01975.hp1 |
synonymous_variant | LOW | c.3156G>A | p.Pro1052Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/17 | 3263/9195 | 3156/4146 | 1052/1381 | chr3 | 125009742 | ||
| chr3:125012933
|
C | T | 1 | a0007c0076 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2646G>A | p.Ser882Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2753/9195 | 2646/4146 | 882/1381 | chr3 | 125012933 | ||
| chr3:125013254
|
A | G | 1 | a0001c0085 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.2325T>C | p.Thr775Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2432/9195 | 2325/4146 | 775/1381 | chr3 | 125013254 | ||
| chr3:125013650
|
C | T | 1 | a0002c0071 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1929G>A | p.Pro643Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2036/9195 | 1929/4146 | 643/1381 | chr3 | 125013650 | ||
| chr3:125019263
|
C | T | 37 | a0001c0001a0001c0002a0001c0010others(34): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
splice_region_variant&synonymous_variant | LOW | c.1587G>A | p.Ser529Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/17 | 1694/9195 | 1587/4146 | 529/1381 | chr3 | 125019263 | ||
| chr3:125021003
|
C | T | 1 | a0042c0079 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1041G>A | p.Thr347Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/17 | 1148/9195 | 1041/4146 | 347/1381 | chr3 | 125021003 | ||
| chr3:125021048
|
G | A | 45 | a0001c0001a0001c0002a0001c0010others(42): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
synonymous_variant | LOW | c.996C>T | p.Ala332Ala | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/17 | 1103/9195 | 996/4146 | 332/1381 | chr3 | 125021048 | ||
| chr3:125027302
|
G | A | 1 | a0016c0052 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.816C>T | p.Thr272Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 923/9195 | 816/4146 | 272/1381 | chr3 | 125027302 | ||
| chr3:125027338
|
C | A | 40 | a0001c0001a0001c0002a0001c0010others(37): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
synonymous_variant | LOW | c.780G>T | p.Pro260Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 887/9195 | 780/4146 | 260/1381 | chr3 | 125027338 | ||
| chr3:125027338
|
C | T | 6 | a0029c0046a0029c0047a0030c0058others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.780G>A | p.Pro260Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 887/9195 | 780/4146 | 260/1381 | chr3 | 125027338 | ||
| chr3:125027395
|
C | T | 1 | a0005c0038 | 2 | HG02135.hp1 NA18997.hp2 |
synonymous_variant | LOW | c.723G>A | p.Gly241Gly | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 830/9195 | 723/4146 | 241/1381 | chr3 | 125027395 | ||
| chr3:125027452
|
G | A | 1 | a0003c0068 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.666C>T | p.Ala222Ala | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 773/9195 | 666/4146 | 222/1381 | chr3 | 125027452 | ||
| chr3:125027503
|
T | C | 74 | a0001c0001a0001c0002a0001c0010others(71): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
synonymous_variant | LOW | c.615A>G | p.Ser205Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 722/9195 | 615/4146 | 205/1381 | chr3 | 125027503 | ||
| chr3:125029382
|
G | A | 34 | a0001c0001a0001c0002a0001c0010others(31): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
synonymous_variant | LOW | c.423C>T | p.Gly141Gly | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/17 | 530/9195 | 423/4146 | 141/1381 | chr3 | 125029382 | ||
| chr3:125055741
|
C | T | 1 | a0010c0056 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.150G>A | p.Ala50Ala | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 257/9195 | 150/4146 | 50/1381 | chr3 | 125055741 | ||
| chr3:125055828
|
C | T | 11 | a0001c0010a0001c0020a0002c0049others(8): Show | 19 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(16): Show |
synonymous_variant | LOW | c.63G>A | p.Leu21Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 170/9195 | 63/4146 | 21/1381 | chr3 | 125055828 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:124965817
|
T | C | 1 | a0059c0057t0128 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4835A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4835 | chr3 | 124965817 | |||||
| chr3:124966122
|
C | T | 240 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(237): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*4530G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4530 | chr3 | 124966122 | |||||
| chr3:124966290
|
G | T | 1 | a0019c0023t0031 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4362C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4362 | chr3 | 124966290 | |||||
| chr3:124966385
|
T | C | 2 | a0004c0033t0094a0043c0075t0076 | 2 | HG01255.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4267A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4267 | chr3 | 124966385 | |||||
| chr3:124966565
|
C | T | 2 | a0001c0001t0126a0056c0092t0133 | 2 | HG02698.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4087G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4087 | chr3 | 124966565 | |||||
| chr3:124966653
|
T | C | 1 | a0005c0007t0129 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3999A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3999 | chr3 | 124966653 | |||||
| chr3:124966728
|
T | C | 13 | a0001c0002t0049a0003c0004t0040a0004c0081t0116others(10): Show | 15 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3924A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3924 | chr3 | 124966728 | |||||
| chr3:124967032
|
A | T | 2 | a0004c0081t0116a0004c0082t0069 | 2 | HG01891.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3620T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3620 | chr3 | 124967032 | |||||
| chr3:124967124
|
T | C | 1 | a0007c0076t0091 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3528A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3528 | chr3 | 124967124 | |||||
| chr3:124967333
|
C | T | 1 | a0001c0010t0107 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3319G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3319 | chr3 | 124967333 | |||||
| chr3:124967387
|
T | C | 2 | a0001c0001t0095a0002c0014t0121 | 2 | NA18994.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3265A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3265 | chr3 | 124967387 | |||||
| chr3:124967413
|
T | C | 13 | a0001c0001t0100a0001c0002t0032a0001c0002t0050others(10): Show | 18 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3239A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3239 | chr3 | 124967413 | |||||
| chr3:124967457
|
A | AT | 71 | a0001c0001t0008a0001c0001t0010a0001c0001t0029others(68): Show | 101 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3194dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3194 | chr3 | 124967457 | |||||
| chr3:124967457
|
AT | A | 89 | a0001c0001t0004a0001c0001t0011a0001c0001t0027others(86): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*3194delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3194 | chr3 | 124967457 | |||||
| chr3:124967457
|
ATT | A | 9 | a0001c0001t0092a0002c0003t0046a0003c0034t0030others(6): Show | 10 | HG02083.hp1 HG02132.hp2 HG02523.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3193_*3194delAA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3193 | chr3 | 124967457 | |||||
| chr3:124967486
|
G | A | 1 | a0005c0007t0123 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3166C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3166 | chr3 | 124967486 | |||||
| chr3:124967663
|
A | G | 208 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(205): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*2989T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2989 | chr3 | 124967663 | |||||
| chr3:124967729
|
G | C | 1 | a0026c0054t0110 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2923C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2923 | chr3 | 124967729 | |||||
| chr3:124967889
|
C | A | 94 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(91): Show | 153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2763G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2763 | chr3 | 124967889 | |||||
| chr3:124968100
|
C | T | 3 | a0007c0077t0073a0027c0032t0065a0059c0057t0128 | 3 | HG02055.hp1 HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2552G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2552 | chr3 | 124968100 | |||||
| chr3:124968125
|
G | C | 1 | a0004c0081t0116 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2527C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2527 | chr3 | 124968125 | |||||
| chr3:124968190
|
T | C | 1 | a0003c0068t0084 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2462A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2462 | chr3 | 124968190 | |||||
| chr3:124968211
|
C | T | 2 | a0004c0081t0116a0004c0082t0069 | 2 | HG01891.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2441G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2441 | chr3 | 124968211 | |||||
| chr3:124968245
|
C | T | 2 | a0001c0001t0126a0001c0001t0127 | 2 | HG01192.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2407G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2407 | chr3 | 124968245 | |||||
| chr3:124968248
|
C | T | 2 | a0004c0081t0116a0004c0082t0069 | 2 | HG01891.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2404G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2404 | chr3 | 124968248 | |||||
| chr3:124968550
|
G | C | 1 | a0006c0006t0088 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2102 | chr3 | 124968550 | |||||
| chr3:124968588
|
G | A | 17 | a0001c0001t0044a0001c0001t0045a0001c0001t0061others(14): Show | 19 | HG00597.hp2 HG01071.hp2 HG01106.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2064C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2064 | chr3 | 124968588 | |||||
| chr3:124968616
|
C | T | 60 | a0001c0001t0006a0001c0002t0103a0002c0003t0002others(57): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*2036G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2036 | chr3 | 124968616 | |||||
| chr3:124968617
|
G | A | 1 | a0001c0002t0051 | 2 | HG00099.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2035 | chr3 | 124968617 | |||||
| chr3:124968677
|
C | T | 1 | a0001c0085t0132 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1975 | chr3 | 124968677 | |||||
| chr3:124968711
|
C | T | 4 | a0001c0002t0104a0009c0027t0140a0009c0027t0144others(1): Show | 5 | HG01167.hp1 HG01361.hp2 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1941G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1941 | chr3 | 124968711 | |||||
| chr3:124968803
|
G | A | 1 | a0002c0003t0089 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1849C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1849 | chr3 | 124968803 | |||||
| chr3:124968923
|
G | T | 183 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(180): Show | 257 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*1729C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1729 | chr3 | 124968923 | |||||
| chr3:124969072
|
G | A | 1 | a0009c0027t0144 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1580C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1580 | chr3 | 124969072 | |||||
| chr3:124969093
|
G | T | 1 | a0014c0019t0102 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1559C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1559 | chr3 | 124969093 | |||||
| chr3:124969425
|
T | C | 87 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(84): Show | 116 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1227A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1227 | chr3 | 124969425 | |||||
| chr3:124969572
|
C | T | 22 | a0001c0001t0007a0002c0003t0007a0002c0003t0015others(19): Show | 34 | HG00639.hp1 HG00733.hp1 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1080G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1080 | chr3 | 124969572 | |||||
| chr3:124969770
|
T | A | 1 | a0008c0060t0139 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 882 | chr3 | 124969770 | |||||
| chr3:124969795
|
C | CA | 190 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(187): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*857insT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 856 | chr3 | 124969795 | |||||
| chr3:124969947
|
A | T | 187 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(184): Show | 264 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*705T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 705 | chr3 | 124969947 | |||||
| chr3:124970157
|
C | T | 22 | a0001c0001t0007a0001c0001t0077a0002c0003t0007others(19): Show | 34 | HG00639.hp1 HG00733.hp1 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*495G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 495 | chr3 | 124970157 | |||||
| chr3:124970158
|
G | A | 1 | a0001c0001t0113 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 494 | chr3 | 124970158 | |||||
| chr3:124970243
|
A | G | 1 | a0001c0002t0072 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 409 | chr3 | 124970243 | |||||
| chr3:124970371
|
C | T | 1 | a0001c0002t0145 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*281G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 281 | chr3 | 124970371 | |||||
| chr3:124970372
|
G | A | 1 | a0014c0019t0114 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 280 | chr3 | 124970372 | |||||
| chr3:124970513
|
C | G | 1 | a0044c0074t0071 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 139 | chr3 | 124970513 | |||||
| chr3:124970559
|
C | T | 5 | a0001c0001t0070a0004c0081t0116a0004c0082t0069others(2): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*93G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 93 | chr3 | 124970559 | |||||
| chr3:124970612
|
G | C | 1 | a0007c0015t0115 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 40 | chr3 | 124970612 | |||||
| chr3:125055935
|
A | AGGGCAGC | 134 | a0001c0001t0007a0001c0001t0010a0001c0001t0011others(131): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
5_prime_UTR_variant | MODIFIER | c.-52_-46dupGCTGCCC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 46 | chr3 | 125055935 | |||||
| chr3:125055935
|
A | AGGGCAGC others(7): Show |
4 | a0027c0032t0065a0034c0066t0068a0035c0065t0066others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-59_-46dupGCTGCCCG others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 46 | chr3 | 125055935 | |||||
| chr3:125055976
|
G | A | 1 | a0001c0002t0145 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 86 | chr3 | 125055976 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:124971268
|
A | G | 7 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193others(4): Show | 7 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.3997-467T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971268 | ||||||
| chr3:124971450
|
C | CT | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 164 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.3997-650dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971450 | ||||||
| chr3:124971478
|
CTTTTCTT others(4): Show |
C | 2 | a0034c0066t0068g0010a0041c0069t0111g0203 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3997-688_3997-678d others(13): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971478 | ||||||
| chr3:124971680
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3997-879G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971680 | ||||||
| chr3:124971789
|
C | CT | 84 | a0001c0001t0070g0194a0001c0002t0001g0143a0001c0002t0016g0046others(81): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3997-989dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971789 | ||||||
| chr3:124971789
|
C | CTT | 158 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(155): Show | 162 | HG00323.hp2 HG00597.hp2 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.3997-990_3997-989d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971789 | ||||||
| chr3:124971789
|
C | CTTT | 23 | a0001c0001t0007g0113a0001c0001t0008g0250a0001c0001t0059g0262others(20): Show | 25 | HG00438.hp2 HG00735.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.3997-991_3997-989d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971789 | ||||||
| chr3:124972148
|
C | T | 1 | a0013c0040t0059g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3997-1347G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972148 | ||||||
| chr3:124972351
|
T | C | 1 | a0038c0084t0019g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3996+1380A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972351 | ||||||
| chr3:124972366
|
A | C | 3 | a0001c0002t0005g0255a0001c0002t0005g0292a0001c0002t0005g0293 | 3 | HG00642.hp2 HG01168.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.3996+1365T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972366 | ||||||
| chr3:124972437
|
T | C | 1 | a0030c0058t0057g0220 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3996+1294A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972437 | ||||||
| chr3:124972480
|
A | G | 1 | a0001c0002t0016g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3996+1251T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972480 | ||||||
| chr3:124972626
|
T | C | 260 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(257): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3996+1105A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972626 | ||||||
| chr3:124972690
|
G | C | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3996+1041C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972690 | ||||||
| chr3:124973007
|
T | G | 168 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(165): Show | 172 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.3996+724A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973007 | ||||||
| chr3:124973008
|
A | T | 168 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(165): Show | 172 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.3996+723T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973008 | ||||||
| chr3:124973015
|
C | CTAT | 91 | a0001c0001t0006g0282a0001c0001t0006g0283a0002c0003t0002g0156others(88): Show | 96 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.3996+713_3996+715d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973015 | ||||||
| chr3:124973056
|
C | T | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3996+675G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973056 | ||||||
| chr3:124973155
|
A | G | 257 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(254): Show | 266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.3996+576T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973155 | ||||||
| chr3:124973173
|
C | T | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3996+558G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973173 | ||||||
| chr3:124973202
|
G | T | 99 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0070g0194others(96): Show | 104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3996+529C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973202 | ||||||
| chr3:124973315
|
G | A | 6 | a0001c0001t0070g0194a0004c0081t0116g0246a0004c0082t0069g0190others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3996+416C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973315 | ||||||
| chr3:124973350
|
T | C | 97 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0070g0194others(94): Show | 102 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3996+381A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973350 | ||||||
| chr3:124973570
|
T | C | 1 | a0011c0008t0027g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3996+161A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973570 | ||||||
| chr3:124973941
|
C | T | 256 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(253): Show | 265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.3822-36G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124973941 | ||||||
| chr3:124974210
|
C | T | 1 | a0004c0005t0011g0197 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3822-305G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974210 | ||||||
| chr3:124974455
|
G | T | 257 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(254): Show | 266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.3822-550C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974455 | ||||||
| chr3:124974494
|
C | T | 1 | a0001c0001t0098g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3822-589G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974494 | ||||||
| chr3:124974674
|
C | T | 102 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(99): Show | 103 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.3822-769G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974674 | ||||||
| chr3:124974690
|
A | T | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-785T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974690 | ||||||
| chr3:124974754
|
G | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-849C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974754 | ||||||
| chr3:124974833
|
G | A | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-928C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974833 | ||||||
| chr3:124974960
|
C | T | 3 | a0020c0025t0025g0008a0020c0025t0130g0318a0030c0058t0057g0220 | 4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3822-1055G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974960 | ||||||
| chr3:124974982
|
C | T | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1077G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974982 | ||||||
| chr3:124974999
|
G | A | 1 | a0007c0015t0005g0287 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3822-1094C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974999 | ||||||
| chr3:124975038
|
T | A | 1 | a0001c0020t0029g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3822-1133A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975038 | ||||||
| chr3:124975079
|
G | A | 1 | a0001c0001t0095g0101 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3822-1174C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975079 | ||||||
| chr3:124975159
|
G | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1254C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975159 | ||||||
| chr3:124975221
|
A | G | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1316T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975221 | ||||||
| chr3:124975247
|
C | T | 1 | a0001c0002t0072g0133 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3822-1342G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975247 | ||||||
| chr3:124975364
|
C | G | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1459G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975364 | ||||||
| chr3:124975459
|
C | T | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1554G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975459 | ||||||
| chr3:124975524
|
A | G | 1 | a0001c0001t0061g0290 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3822-1619T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975524 | ||||||
| chr3:124975558
|
G | A | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1653C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975558 | ||||||
| chr3:124975634
|
C | G | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1729G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975634 | ||||||
| chr3:124975695
|
T | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1790A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975695 | ||||||
| chr3:124975842
|
T | C | 1 | a0001c0010t0107g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3822-1937A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975842 | ||||||
| chr3:124975875
|
G | A | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1970C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975875 | ||||||
| chr3:124975902
|
T | A | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1957A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975902 | ||||||
| chr3:124975975
|
G | A | 1 | a0005c0007t0129g0347 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3821+1884C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975975 | ||||||
| chr3:124975985
|
G | A | 1 | a0001c0001t0099g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3821+1874C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975985 | ||||||
| chr3:124976034
|
G | A | 23 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(20): Show | 26 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.3821+1825C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976034 | ||||||
| chr3:124976093
|
G | A | 1 | a0011c0008t0036g0240 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3821+1766C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976093 | ||||||
| chr3:124976187
|
G | A | 92 | a0001c0001t0006g0282a0001c0001t0006g0283a0002c0003t0002g0156others(89): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3821+1672C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976187 | ||||||
| chr3:124976250
|
T | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1609A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976250 | ||||||
| chr3:124976259
|
G | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1600C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976259 | ||||||
| chr3:124976268
|
C | A | 1 | a0055c0090t0119g0350 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3821+1591G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976268 | ||||||
| chr3:124976270
|
T | G | 2 | a0001c0002t0016g0046a0001c0002t0033g0045 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3821+1589A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976270 | ||||||
| chr3:124976497
|
AT | A | 164 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(161): Show | 168 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.3821+1361delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976497 | ||||||
| chr3:124976610
|
C | T | 1 | a0006c0086t0090g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3821+1249G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976610 | ||||||
| chr3:124976733
|
G | T | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1126C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976733 | ||||||
| chr3:124976840
|
T | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1019A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976840 | ||||||
| chr3:124976882
|
C | T | 3 | a0002c0003t0007g0148a0007c0011t0011g0060a0007c0011t0011g0124 | 3 | HG00642.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3821+977G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976882 | ||||||
| chr3:124976964
|
G | A | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+895C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976964 | ||||||
| chr3:124976977
|
T | C | 1 | a0027c0032t0065g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3821+882A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976977 | ||||||
| chr3:124977068
|
C | CATGATAG others(3): Show |
160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+781_3821+790d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977068 | ||||||
| chr3:124977212
|
C | T | 55 | a0001c0001t0070g0194a0001c0001t0077g0043a0001c0001t0126g0274others(52): Show | 57 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3821+647G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977212 | ||||||
| chr3:124977335
|
T | C | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+524A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977335 | ||||||
| chr3:124977667
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3821+192A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977667 | ||||||
| chr3:124977714
|
C | T | 1 | a0006c0006t0088g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3821+145G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977714 | ||||||
| chr3:124977953
|
G | A | 1 | a0010c0022t0062g0231 | 1 | NA19054.hp2 | splice_region_variant&intron_variant | LOW | c.3734-7C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124977953 | ||||||
| chr3:124977963
|
CA | C | 102 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(99): Show | 103 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.3734-18delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124977963 | ||||||
| chr3:124978100
|
A | G | 1 | a0001c0002t0049g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3734-154T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978100 | ||||||
| chr3:124978141
|
G | T | 4 | a0001c0001t0070g0194a0022c0026t0053g0304a0022c0026t0053g0305others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734-195C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978141 | ||||||
| chr3:124978383
|
T | G | 165 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(162): Show | 169 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.3734-437A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978383 | ||||||
| chr3:124978639
|
T | C | 1 | a0001c0001t0127g0301 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3734-693A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978639 | ||||||
| chr3:124978763
|
T | G | 1 | a0008c0013t0124g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3734-817A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978763 | ||||||
| chr3:124978802
|
A | AAAAT | 145 | a0001c0001t0007g0113a0001c0001t0008g0247a0001c0001t0008g0250others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.3734-860_3734-857d others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | ||||||
| chr3:124978802
|
A | AAAATAAA others(1): Show |
109 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(106): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.3734-864_3734-857d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | ||||||
| chr3:124978802
|
A | AAAATAAA others(5): Show |
27 | a0001c0001t0097g0144a0002c0003t0006g0267a0003c0004t0009g0072others(24): Show | 29 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.3734-868_3734-857d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | ||||||
| chr3:124978802
|
AAAATAAA others(1): Show |
A | 7 | a0003c0004t0040g0174a0003c0004t0040g0175a0029c0047t0108g0018others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3734-864_3734-857d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | ||||||
| chr3:124978802
|
AAAATAAA others(5): Show |
A | 2 | a0004c0005t0028g0259a0056c0092t0133g0316 | 2 | HG03139.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3734-868_3734-857d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | ||||||
| chr3:124978956
|
C | CT | 12 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3734-1011dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978956 | ||||||
| chr3:124978987
|
G | A | 2 | a0003c0068t0084g0196a0006c0006t0009g0042 | 2 | HG00738.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3734-1041C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978987 | ||||||
| chr3:124979019
|
C | T | 1 | a0009c0027t0140g0331 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3734-1073G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979019 | ||||||
| chr3:124979140
|
C | T | 2 | a0006c0086t0090g0084a0007c0076t0091g0161 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3734-1194G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979140 | ||||||
| chr3:124979148
|
C | T | 92 | a0001c0001t0006g0282a0001c0001t0006g0283a0002c0003t0002g0156others(89): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3734-1202G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979148 | ||||||
| chr3:124979613
|
T | C | 2 | a0006c0086t0090g0084a0007c0076t0091g0161 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3734-1667A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979613 | ||||||
| chr3:124979760
|
C | T | 28 | a0001c0001t0126g0274a0001c0001t0127g0301a0002c0003t0002g0156others(25): Show | 31 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.3734-1814G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979760 | ||||||
| chr3:124980299
|
T | A | 1 | a0004c0082t0069g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3734-2353A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980299 | ||||||
| chr3:124980358
|
A | T | 13 | a0001c0001t0044g0103a0001c0001t0044g0160a0001c0001t0045g0128others(10): Show | 13 | HG01071.hp2 HG01106.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.3734-2412T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980358 | ||||||
| chr3:124980402
|
T | G | 257 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(254): Show | 266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.3734-2456A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980402 | ||||||
| chr3:124980497
|
C | T | 5 | a0007c0011t0022g0002a0007c0011t0086g0080a0036c0064t0067g0009others(2): Show | 6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3734-2551G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980497 | ||||||
| chr3:124980549
|
C | T | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-2603G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980549 | ||||||
| chr3:124980665
|
C | T | 5 | a0002c0003t0003g0004a0002c0003t0003g0005a0002c0003t0003g0105others(2): Show | 7 | HG00544.hp2 NA18944.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.3734-2719G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980665 | ||||||
| chr3:124980871
|
T | G | 1 | a0021c0043t0063g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3734-2925A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980871 | ||||||
| chr3:124981004
|
C | T | 1 | a0003c0004t0014g0285 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3734-3058G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981004 | ||||||
| chr3:124981014
|
G | T | 1 | a0001c0002t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3734-3068C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981014 | ||||||
| chr3:124981064
|
C | G | 51 | a0001c0001t0070g0194a0001c0001t0077g0043a0002c0003t0007g0069others(48): Show | 53 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.3734-3118G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981064 | ||||||
| chr3:124981071
|
C | T | 256 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(253): Show | 265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.3734-3125G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981071 | ||||||
| chr3:124981233
|
C | CT | 181 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0126g0274others(178): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.3734-3288dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981233 | ||||||
| chr3:124981233
|
C | CTTT | 52 | a0001c0001t0070g0194a0001c0001t0077g0043a0002c0003t0007g0069others(49): Show | 55 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.3734-3290_3734-328 others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981233 | ||||||
| chr3:124981248
|
A | T | 99 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(96): Show | 100 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3734-3302T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981248 | ||||||
| chr3:124981251
|
G | A | 99 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(96): Show | 100 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3734-3305C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981251 | ||||||
| chr3:124981251
|
GT | G | 60 | a0001c0001t0004g0295a0001c0001t0008g0248a0001c0001t0008g0294others(57): Show | 63 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.3734-3306delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981251 | ||||||
| chr3:124981252
|
T | G | 99 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(96): Show | 100 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3734-3306A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981252 | ||||||
| chr3:124981350
|
G | C | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-3404C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981350 | ||||||
| chr3:124981492
|
C | T | 1 | a0001c0002t0103g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3734-3546G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981492 | ||||||
| chr3:124981549
|
A | G | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-3603T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981549 | ||||||
| chr3:124981566
|
C | T | 1 | a0007c0011t0011g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3734-3620G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981566 | ||||||
| chr3:124981570
|
G | A | 6 | a0001c0001t0126g0274a0001c0001t0127g0301a0003c0004t0040g0174others(3): Show | 6 | HG01192.hp1 HG01891.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3734-3624C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981570 | ||||||
| chr3:124981868
|
A | C | 158 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(155): Show | 162 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.3734-3922T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981868 | ||||||
| chr3:124981871
|
C | T | 1 | a0004c0005t0010g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3734-3925G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981871 | ||||||
| chr3:124981912
|
ATT | A | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-3968_3734-396 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981912 | ||||||
| chr3:124981945
|
C | T | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3734-3999G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981945 | ||||||
| chr3:124981946
|
A | G | 105 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(102): Show | 106 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.3734-4000T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981946 | ||||||
| chr3:124982142
|
C | T | 1 | a0026c0054t0110g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3734-4196G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982142 | ||||||
| chr3:124982265
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3734-4319A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982265 | ||||||
| chr3:124982274
|
G | C | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-4328C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982274 | ||||||
| chr3:124982333
|
T | A | 1 | a0030c0058t0057g0220 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3734-4387A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982333 | ||||||
| chr3:124982344
|
T | C | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-4398A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982344 | ||||||
| chr3:124982390
|
C | T | 4 | a0001c0001t0093g0162a0004c0005t0010g0165a0018c0088t0010g0177others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3734-4444G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982390 | ||||||
| chr3:124982426
|
G | A | 1 | a0029c0047t0108g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3734-4480C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982426 | ||||||
| chr3:124982603
|
A | G | 1 | a0003c0004t0002g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3734-4657T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982603 | ||||||
| chr3:124982646
|
G | C | 4 | a0018c0037t0063g0256a0018c0037t0109g0186a0021c0043t0063g0342others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734-4700C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982646 | ||||||
| chr3:124982762
|
C | T | 1 | a0010c0056t0143g0210 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3734-4816G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982762 | ||||||
| chr3:124982964
|
TG | T | 4 | a0007c0011t0022g0002a0007c0011t0086g0080a0036c0064t0067g0009others(1): Show | 5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3734-5019delC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982964 | ||||||
| chr3:124983087
|
C | A | 1 | a0001c0010t0001g0013 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3734-5141G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983087 | ||||||
| chr3:124983160
|
C | A | 1 | a0005c0007t0129g0347 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3734-5214G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983160 | ||||||
| chr3:124983164
|
C | A | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5218G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983164 | ||||||
| chr3:124983203
|
C | T | 1 | a0006c0006t0002g0098 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3734-5257G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983203 | ||||||
| chr3:124983338
|
T | C | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5392A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983338 | ||||||
| chr3:124983346
|
CT | C | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5401delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983346 | ||||||
| chr3:124983407
|
T | G | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5461A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983407 | ||||||
| chr3:124983421
|
C | CA | 158 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(155): Show | 162 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.3734-5476dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983421 | ||||||
| chr3:124983423
|
C | A | 1 | a0001c0001t0004g0295 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3734-5477G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983423 | ||||||
| chr3:124983463
|
C | T | 254 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(251): Show | 258 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.3734-5517G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983463 | ||||||
| chr3:124983501
|
A | AT | 161 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0279others(158): Show | 165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3734-5556dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983501 | ||||||
| chr3:124983580
|
C | T | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5634G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983580 | ||||||
| chr3:124983605
|
G | C | 1 | a0001c0001t0011g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3734-5659C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983605 | ||||||
| chr3:124983700
|
C | T | 1 | a0003c0004t0002g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3734-5754G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983700 | ||||||
| chr3:124983754
|
C | T | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3734-5808G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983754 | ||||||
| chr3:124983791
|
T | C | 1 | a0001c0001t0099g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3734-5845A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983791 | ||||||
| chr3:124983794
|
T | C | 1 | a0004c0035t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3734-5848A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983794 | ||||||
| chr3:124983808
|
T | C | 4 | a0018c0037t0063g0256a0018c0037t0109g0186a0021c0043t0063g0342others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734-5862A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983808 | ||||||
| chr3:124984173
|
G | A | 2 | a0001c0001t0126g0274a0001c0001t0127g0301 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3734-6227C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984173 | ||||||
| chr3:124984177
|
G | T | 2 | a0006c0006t0009g0141a0016c0029t0020g0034 | 2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3734-6231C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984177 | ||||||
| chr3:124984215
|
G | T | 6 | a0001c0001t0126g0274a0001c0001t0127g0301a0003c0004t0040g0174others(3): Show | 6 | HG01192.hp1 HG01891.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3734-6269C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984215 | ||||||
| chr3:124984263
|
C | G | 161 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(158): Show | 165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3734-6317G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984263 | ||||||
| chr3:124984270
|
C | T | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3734-6324G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984270 | ||||||
| chr3:124984359
|
C | CAT | 161 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(158): Show | 165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3734-6414_3734-641 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984359 | ||||||
| chr3:124984381
|
T | C | 5 | a0007c0011t0022g0002a0007c0011t0086g0080a0036c0064t0067g0009others(2): Show | 6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+6406A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984381 | ||||||
| chr3:124984450
|
G | A | 6 | a0001c0001t0070g0194a0004c0081t0116g0246a0004c0082t0069g0190others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3733+6337C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984450 | ||||||
| chr3:124984512
|
G | A | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG00609.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3733+6275C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984512 | ||||||
| chr3:124984575
|
A | T | 2 | a0003c0004t0039g0053a0003c0045t0039g0026 | 2 | HG02735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3733+6212T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984575 | ||||||
| chr3:124984604
|
C | T | 1 | a0006c0006t0118g0297 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3733+6183G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984604 | ||||||
| chr3:124984684
|
G | A | 1 | a0001c0001t0018g0253 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3733+6103C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984684 | ||||||
| chr3:124984753
|
C | G | 50 | a0001c0001t0070g0194a0001c0001t0077g0043a0002c0003t0007g0069others(47): Show | 52 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.3733+6034G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984753 | ||||||
| chr3:124984849
|
A | C | 95 | a0001c0002t0001g0074a0001c0002t0001g0079a0001c0002t0001g0091others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3733+5938T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984849 | ||||||
| chr3:124985033
|
G | A | 2 | a0005c0007t0060g0334a0005c0007t0137g0337 | 2 | HG02155.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3733+5754C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985033 | ||||||
| chr3:124985062
|
G | A | 1 | a0040c0078t0015g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3733+5725C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985062 | ||||||
| chr3:124985211
|
A | G | 2 | a0001c0001t0126g0274a0001c0001t0127g0301 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3733+5576T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985211 | ||||||
| chr3:124985216
|
G | A | 1 | a0018c0037t0063g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3733+5571C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985216 | ||||||
| chr3:124985380
|
A | C | 1 | a0003c0004t0002g0169 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3733+5407T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985380 | ||||||
| chr3:124985402
|
AT | A | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+5384delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985402 | ||||||
| chr3:124985405
|
T | G | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+5382A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985405 | ||||||
| chr3:124985589
|
G | A | 159 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(156): Show | 163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3733+5198C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985589 | ||||||
| chr3:124985797
|
T | G | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+4990A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985797 | ||||||
| chr3:124986131
|
G | A | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG00609.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3733+4656C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986131 | ||||||
| chr3:124986267
|
A | G | 262 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(259): Show | 266 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.3733+4520T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986267 | ||||||
| chr3:124986368
|
A | G | 161 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(158): Show | 165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3733+4419T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986368 | ||||||
| chr3:124986411
|
T | G | 161 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(158): Show | 165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3733+4376A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986411 | ||||||
| chr3:124986497
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3733+4290G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986497 | ||||||
| chr3:124986583
|
T | C | 2 | a0004c0081t0116g0246a0004c0082t0069g0190 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3733+4204A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986583 | ||||||
| chr3:124986658
|
G | A | 2 | a0006c0006t0002g0178a0039c0087t0021g0090 | 2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.3733+4129C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986658 | ||||||
| chr3:124986819
|
G | T | 1 | a0022c0026t0117g0306 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3733+3968C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986819 | ||||||
| chr3:124987108
|
C | T | 1 | a0001c0001t0099g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3733+3679G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987108 | ||||||
| chr3:124987290
|
T | C | 1 | a0050c0050t0022g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3733+3497A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987290 | ||||||
| chr3:124987374
|
G | GCCACACC others(1): Show |
9 | a0007c0011t0011g0060a0007c0011t0011g0124a0009c0009t0004g0330others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3733+3405_3733+341 others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987374 | ||||||
| chr3:124987474
|
C | G | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+3313G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987474 | ||||||
| chr3:124987570
|
C | T | 108 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(105): Show | 109 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.3733+3217G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987570 | ||||||
| chr3:124987577
|
C | CA | 5 | a0007c0011t0022g0002a0007c0011t0086g0080a0036c0064t0067g0009others(2): Show | 6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+3209dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987577 | ||||||
| chr3:124987579
|
A | G | 1 | a0009c0009t0061g0321 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3733+3208T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987579 | ||||||
| chr3:124987630
|
T | TCTC | 162 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(159): Show | 166 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.3733+3156_3733+315 others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987630 | ||||||
| chr3:124987789
|
A | G | 261 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(258): Show | 265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3733+2998T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987789 | ||||||
| chr3:124987847
|
A | G | 3 | a0020c0025t0025g0008a0020c0025t0130g0318a0030c0058t0057g0220 | 4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2940T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987847 | ||||||
| chr3:124987924
|
T | TAC | 5 | a0006c0006t0009g0141a0006c0006t0054g0249a0016c0029t0020g0034others(2): Show | 5 | HG00323.hp1 HG01106.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2861_3733+286 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACAC | 3 | a0003c0004t0040g0175a0006c0006t0022g0088a0047c0080t0085g0086 | 3 | HG01891.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3733+2857_3733+286 others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(3): Show |
1 | a0006c0086t0090g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3733+2853_3733+286 others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(7): Show |
10 | a0001c0001t0007g0113a0001c0001t0018g0253a0001c0001t0029g0153others(7): Show | 10 | HG00639.hp2 HG01081.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.3733+2849_3733+286 others(18): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(9): Show |
13 | a0001c0001t0044g0103a0001c0001t0097g0144a0001c0001t0100g0095others(10): Show | 13 | HG01243.hp2 HG01256.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.3733+2847_3733+286 others(20): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(11): Show |
6 | a0001c0001t0059g0262a0001c0001t0070g0194a0001c0001t0127g0301others(3): Show | 6 | HG01109.hp2 HG01192.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.3733+2845_3733+286 others(22): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(13): Show |
5 | a0004c0081t0116g0246a0011c0008t0004g0238a0019c0023t0031g0193others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2843_3733+286 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(15): Show |
3 | a0019c0023t0031g0192a0029c0047t0108g0018a0034c0066t0068g0010 | 3 | HG02615.hp1 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3733+2841_3733+286 others(26): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
T | TACACACA others(17): Show |
3 | a0004c0082t0069g0190a0019c0023t0031g0182a0041c0069t0111g0203 | 3 | HG02630.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3733+2839_3733+286 others(28): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987924
|
TAC | T | 57 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(54): Show | 60 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.3733+2861_3733+286 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | ||||||
| chr3:124987944
|
C | T | 2 | a0001c0002t0024g0092a0001c0002t0024g0093 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3733+2843G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987944 | ||||||
| chr3:124987952
|
C | CACACACA others(39): Show |
1 | a0005c0007t0013g0338 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(45): Show |
1 | a0009c0027t0144g0328 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(56): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(47): Show |
1 | a0002c0014t0121g0257 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(33): Show |
1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
1 | a0002c0003t0015g0083 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(37): Show |
1 | a0001c0002t0038g0245 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(41): Show |
3 | a0001c0001t0077g0043a0001c0002t0001g0143a0010c0016t0005g0222 | 3 | HG02083.hp2 HG02523.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
1 | a0005c0007t0060g0335 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(31): Show |
2 | a0002c0003t0007g0069a0002c0003t0074g0075 | 2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
1 | a0006c0006t0118g0297 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(39): Show |
2 | a0028c0036t0030g0067a0028c0036t0030g0119 | 2 | HG02132.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(47): Show |
1 | a0001c0002t0038g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(21): Show |
1 | a0016c0029t0007g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(32): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
3 | a0002c0003t0007g0076a0005c0007t0060g0334a0043c0075t0076g0181 | 3 | HG01255.hp1 HG02155.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(31): Show |
3 | a0005c0007t0137g0337a0025c0030t0048g0036a0055c0090t0119g0350 | 3 | HG00639.hp1 HG01517.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(33): Show |
8 | a0002c0003t0007g0070a0002c0014t0120g0263a0005c0007t0013g0307others(5): Show | 9 | HG01243.hp1 HG02135.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
2 | a0001c0002t0005g0298a0008c0012t0013g0228 | 2 | HG02559.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(37): Show |
3 | a0008c0012t0017g0226a0014c0019t0102g0206a0033c0063t0005g0239 | 3 | HG03710.hp2 NA19055.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(39): Show |
2 | a0001c0002t0005g0292a0001c0002t0024g0115 | 2 | HG00642.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(41): Show |
2 | a0001c0010t0001g0022a0001c0010t0033g0019 | 2 | HG02293.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(43): Show |
1 | a0001c0002t0104g0179 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(54): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(45): Show |
3 | a0001c0002t0005g0293a0001c0002t0024g0138a0025c0030t0048g0037 | 3 | HG01168.hp2 HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(56): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(27): Show |
1 | a0005c0007t0136g0319 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
7 | a0001c0010t0107g0020a0002c0003t0007g0082a0002c0003t0007g0100others(4): Show | 7 | HG01884.hp1 HG02074.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(31): Show |
2 | a0001c0002t0001g0127a0005c0039t0017g0340 | 2 | NA19003.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(33): Show |
4 | a0001c0002t0005g0255a0002c0003t0046g0117a0002c0014t0075g0078others(1): Show | 4 | HG02148.hp2 NA18988.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
4 | a0001c0002t0051g0137a0001c0002t0112g0149a0002c0014t0015g0116others(1): Show | 4 | HG01256.hp1 NA18968.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(37): Show |
6 | a0001c0002t0001g0130a0001c0002t0145g0353a0005c0039t0017g0325others(3): Show | 6 | HG01071.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(39): Show |
1 | a0001c0010t0001g0013 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(41): Show |
1 | a0014c0019t0001g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(45): Show |
2 | a0001c0002t0001g0129a0001c0002t0001g0142 | 2 | HG01928.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(56): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(47): Show |
1 | a0007c0015t0115g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(13): Show |
14 | a0001c0001t0008g0294a0001c0001t0047g0122a0001c0001t0047g0123others(11): Show | 14 | HG00621.hp1 HG00642.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(27): Show |
1 | a0001c0002t0001g0132 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
2 | a0001c0002t0001g0091a0001c0002t0072g0133 | 2 | HG03669.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(31): Show |
3 | a0001c0002t0001g0120a0001c0002t0052g0135a0009c0027t0005g0333 | 3 | HG03239.hp1 NA18950.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(33): Show |
2 | a0001c0002t0024g0093a0003c0034t0030g0114 | 2 | HG03239.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
2 | a0001c0002t0024g0092a0014c0019t0114g0205 | 2 | HG03491.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(37): Show |
6 | a0001c0002t0001g0096a0001c0002t0016g0051a0001c0002t0033g0050others(3): Show | 6 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(39): Show |
2 | a0001c0002t0105g0139a0001c0010t0001g0024 | 2 | HG04115.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(41): Show |
1 | a0001c0002t0051g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(43): Show |
1 | a0004c0035t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(54): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(47): Show |
1 | a0001c0002t0049g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(22): Show |
1 | a0007c0015t0050g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(33): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(11): Show |
29 | a0001c0001t0004g0295a0001c0001t0011g0183a0001c0001t0012g0172others(26): Show | 29 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(22): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(13): Show |
3 | a0004c0005t0028g0259a0013c0040t0059g0315a0015c0017t0045g0131 | 3 | HG02486.hp1 NA18939.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(15): Show |
1 | a0001c0001t0044g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(26): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(25): Show |
1 | a0001c0002t0106g0094 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(36): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(27): Show |
1 | a0001c0002t0050g0198 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
1 | a0040c0078t0015g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(33): Show |
5 | a0001c0002t0001g0107a0001c0002t0005g0302a0001c0002t0016g0145others(2): Show | 5 | HG01074.hp1 HG01099.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
1 | a0001c0002t0103g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(37): Show |
1 | a0001c0002t0016g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(9): Show |
20 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(17): Show | 20 | HG01106.hp1 HG01884.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(20): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(13): Show |
1 | a0001c0001t0010g0068 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(23): Show |
2 | a0006c0006t0088g0065a0059c0057t0128g0211 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(34): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
1 | a0026c0054t0110g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(31): Show |
3 | a0001c0010t0001g0030a0007c0011t0086g0080a0010c0016t0141g0224 | 3 | HG02698.hp1 HG03486.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
1 | a0036c0064t0067g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(7): Show |
16 | a0001c0001t0008g0248a0001c0001t0008g0250a0001c0001t0008g0266others(13): Show | 17 | HG00438.hp2 HG01346.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(18): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(9): Show |
1 | a0007c0011t0011g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(20): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(11): Show |
3 | a0001c0001t0008g0244a0001c0001t0008g0247a0007c0011t0010g0191 | 3 | HG01109.hp1 HG02293.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(22): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(17): Show |
1 | a0001c0002t0032g0200 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(28): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(19): Show |
2 | a0001c0002t0005g0300a0001c0002t0032g0199 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(30): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(23): Show |
1 | a0010c0016t0038g0219 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(34): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(25): Show |
2 | a0001c0002t0001g0074a0001c0002t0001g0079 | 2 | NA18942.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(36): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(27): Show |
1 | a0007c0011t0022g0002 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(29): Show |
1 | a0026c0053t0001g0033 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(13): Show |
1 | a0001c0002t0032g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(3): Show |
1 | a0001c0001t0095g0101 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(25): Show |
1 | a0004c0035t0001g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(36): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CACACACA others(35): Show |
1 | a0051c0095t0057g0317 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | CAT | 5 | a0001c0001t0006g0282a0001c0001t0006g0283a0006c0006t0014g0270others(2): Show | 5 | HG00609.hp1 HG02132.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2833_3733+283 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987952
|
C | T | 3 | a0002c0003t0082g0184a0003c0045t0039g0026a0003c0068t0084g0196 | 3 | HG00738.hp1 HG02735.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3733+2835G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | ||||||
| chr3:124987954
|
T | C | 25 | a0001c0001t0070g0194a0001c0001t0126g0274a0001c0001t0127g0301others(22): Show | 26 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.3733+2833A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987954 | ||||||
| chr3:124987956
|
T | C | 14 | a0001c0001t0126g0274a0001c0001t0127g0301a0008c0060t0139g0218others(11): Show | 15 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3733+2831A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987956 | ||||||
| chr3:124987958
|
T | C | 6 | a0020c0025t0025g0008a0020c0025t0130g0318a0022c0026t0053g0304others(3): Show | 7 | HG00735.hp2 HG01074.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3733+2829A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987958 | ||||||
| chr3:124987960
|
T | C | 3 | a0020c0025t0025g0008a0020c0025t0130g0318a0030c0058t0057g0220 | 4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2827A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987960 | ||||||
| chr3:124987962
|
T | C | 3 | a0020c0025t0025g0008a0020c0025t0130g0318a0030c0058t0057g0220 | 4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2825A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987962 | ||||||
| chr3:124988018
|
A | C | 240 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3733+2769T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988018 | ||||||
| chr3:124988211
|
G | C | 5 | a0007c0011t0022g0002a0007c0011t0086g0080a0036c0064t0067g0009others(2): Show | 6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+2576C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988211 | ||||||
| chr3:124988306
|
A | G | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3733+2481T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988306 | ||||||
| chr3:124988431
|
A | G | 240 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3733+2356T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988431 | ||||||
| chr3:124988455
|
T | C | 1 | a0001c0001t0061g0290 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3733+2332A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988455 | ||||||
| chr3:124988601
|
T | C | 2 | a0017c0024t0037g0007a0017c0024t0037g0265 | 3 | NA18944.hp1 NA18973.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3733+2186A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988601 | ||||||
| chr3:124988744
|
C | T | 4 | a0018c0037t0063g0256a0018c0037t0109g0186a0021c0043t0063g0342others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2043G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988744 | ||||||
| chr3:124988745
|
C | A | 2 | a0003c0004t0081g0176a0005c0007t0123g0351 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3733+2042G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988745 | ||||||
| chr3:124988866
|
G | A | 4 | a0011c0008t0004g0238a0011c0008t0036g0240a0011c0008t0036g0241others(1): Show | 4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+1921C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988866 | ||||||
| chr3:124988933
|
A | G | 4 | a0029c0047t0108g0018a0030c0059t0058g0221a0034c0066t0068g0010others(1): Show | 4 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3733+1854T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988933 | ||||||
| chr3:124988951
|
C | T | 206 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.3733+1836G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988951 | ||||||
| chr3:124989446
|
T | C | 3 | a0012c0041t0035g0310a0012c0041t0035g0312a0054c0091t0122g0311 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3733+1341A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989446 | ||||||
| chr3:124989506
|
CA | C | 206 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.3733+1280delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989506 | ||||||
| chr3:124989718
|
C | G | 1 | a0030c0058t0057g0220 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3733+1069G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989718 | ||||||
| chr3:124989738
|
A | G | 240 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3733+1049T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989738 | ||||||
| chr3:124989815
|
G | C | 1 | a0035c0065t0066g0012 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3733+972C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989815 | ||||||
| chr3:124989923
|
T | C | 1 | a0001c0002t0038g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3733+864A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989923 | ||||||
| chr3:124989985
|
T | C | 206 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.3733+802A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989985 | ||||||
| chr3:124990082
|
C | A | 10 | a0006c0086t0090g0084a0007c0076t0091g0161a0019c0023t0031g0182others(7): Show | 10 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3733+705G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990082 | ||||||
| chr3:124990084
|
C | T | 1 | a0001c0001t0007g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3733+703G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990084 | ||||||
| chr3:124990141
|
T | C | 3 | a0012c0041t0035g0310a0012c0041t0035g0312a0054c0091t0122g0311 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3733+646A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990141 | ||||||
| chr3:124990341
|
G | GT | 6 | a0001c0001t0004g0277a0001c0001t0008g0294a0002c0003t0007g0076others(3): Show | 6 | NA18946.hp2 NA18966.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+445dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990341 | ||||||
| chr3:124990341
|
GT | G | 92 | a0001c0002t0001g0074a0001c0002t0001g0079a0001c0002t0001g0091others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3733+445delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990341 | ||||||
| chr3:124990407
|
T | C | 261 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(258): Show | 265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3733+380A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990407 | ||||||
| chr3:124990528
|
G | A | 1 | a0003c0004t0002g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3733+259C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990528 | ||||||
| chr3:124990570
|
C | A | 4 | a0011c0008t0004g0238a0011c0008t0036g0240a0011c0008t0036g0241others(1): Show | 4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+217G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990570 | ||||||
| chr3:124990592
|
A | G | 1 | a0005c0007t0129g0347 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3733+195T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990592 | ||||||
| chr3:124990652
|
C | T | 1 | a0019c0023t0031g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3733+135G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990652 | ||||||
| chr3:124990654
|
C | A | 1 | a0001c0002t0001g0107 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3733+133G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990654 | ||||||
| chr3:124991054
|
G | A | 37 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(34): Show | 38 | HG00438.hp2 HG00639.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.3653-68C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991054 | ||||||
| chr3:124991150
|
C | CT | 134 | a0001c0001t0070g0194a0001c0001t0077g0043a0001c0002t0001g0074others(131): Show | 137 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.3653-165dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991150 | ||||||
| chr3:124991163
|
T | C | 1 | a0052c0094t0004g0332 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3653-177A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991163 | ||||||
| chr3:124991163
|
T | TC | 104 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(101): Show | 105 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3653-178_3653-177i others(3): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991163 | ||||||
| chr3:124991180
|
C | T | 1 | a0001c0002t0001g0074 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3653-194G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991180 | ||||||
| chr3:124991228
|
C | T | 1 | a0007c0076t0091g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3653-242G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991228 | ||||||
| chr3:124991248
|
C | T | 105 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(102): Show | 106 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.3653-262G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991248 | ||||||
| chr3:124991337
|
A | G | 1 | a0005c0007t0060g0335 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3653-351T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991337 | ||||||
| chr3:124991397
|
C | T | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3653-411G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991397 | ||||||
| chr3:124991528
|
T | C | 240 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3653-542A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991528 | ||||||
| chr3:124991796
|
G | A | 15 | a0006c0086t0090g0084a0007c0076t0091g0161a0008c0060t0139g0218others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3653-810C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991796 | ||||||
| chr3:124991833
|
C | T | 9 | a0007c0011t0011g0060a0007c0011t0011g0124a0009c0009t0004g0330others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3653-847G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991833 | ||||||
| chr3:124991853
|
G | A | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3653-867C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991853 | ||||||
| chr3:124991991
|
T | TC | 9 | a0002c0003t0003g0003a0002c0003t0003g0004a0002c0003t0003g0005others(6): Show | 12 | HG00544.hp2 HG00673.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.3653-1006dupG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991991 | ||||||
| chr3:124992033
|
A | C | 1 | a0008c0013t0004g0212 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3653-1047T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992033 | ||||||
| chr3:124992124
|
G | A | 1 | a0003c0004t0021g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3653-1138C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992124 | ||||||
| chr3:124992163
|
T | C | 1 | a0045c0073t0056g0299 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3653-1177A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992163 | ||||||
| chr3:124992229
|
G | T | 1 | a0029c0047t0108g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3653-1243C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992229 | ||||||
| chr3:124992237
|
G | A | 1 | a0004c0005t0042g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3653-1251C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992237 | ||||||
| chr3:124992251
|
A | G | 243 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(240): Show | 247 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.3653-1265T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992251 | ||||||
| chr3:124992348
|
A | G | 1 | a0055c0090t0119g0350 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3653-1362T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992348 | ||||||
| chr3:124992491
|
C | T | 19 | a0001c0001t0012g0172a0001c0001t0042g0097a0004c0005t0004g0278others(16): Show | 19 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.3653-1505G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992491 | ||||||
| chr3:124992527
|
C | T | 107 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(104): Show | 108 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.3653-1541G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992527 | ||||||
| chr3:124992542
|
G | A | 107 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(104): Show | 108 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.3653-1556C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992542 | ||||||
| chr3:124992991
|
A | G | 2 | a0007c0015t0005g0269a0007c0015t0049g0058 | 2 | HG00544.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3653-2005T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992991 | ||||||
| chr3:124992992
|
C | T | 10 | a0006c0086t0090g0084a0007c0076t0091g0161a0019c0023t0031g0182others(7): Show | 10 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3653-2006G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992992 | ||||||
| chr3:124993024
|
C | T | 1 | a0006c0006t0019g0110 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3653-2038G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993024 | ||||||
| chr3:124993122
|
T | G | 33 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(30): Show | 34 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.3653-2136A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993122 | ||||||
| chr3:124993188
|
C | T | 1 | a0001c0001t0018g0253 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3653-2202G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993188 | ||||||
| chr3:124993309
|
T | C | 1 | a0004c0082t0069g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3653-2323A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993309 | ||||||
| chr3:124993322
|
C | T | 2 | a0003c0004t0002g0056a0003c0004t0021g0057 | 2 | HG00438.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.3653-2336G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993322 | ||||||
| chr3:124993324
|
C | T | 1 | a0027c0032t0065g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3653-2338G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993324 | ||||||
| chr3:124993352
|
A | T | 51 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(48): Show | 52 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.3653-2366T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993352 | ||||||
| chr3:124993412
|
T | C | 1 | a0018c0037t0063g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3653-2426A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993412 | ||||||
| chr3:124993466
|
T | C | 259 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.3653-2480A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993466 | ||||||
| chr3:124993485
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3653-2499G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993485 | ||||||
| chr3:124993491
|
T | C | 259 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.3653-2505A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993491 | ||||||
| chr3:124993552
|
A | G | 111 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(108): Show | 112 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.3653-2566T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993552 | ||||||
| chr3:124993571
|
A | G | 259 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.3653-2585T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993571 | ||||||
| chr3:124993643
|
G | A | 2 | a0001c0001t0126g0274a0001c0001t0127g0301 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3653-2657C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993643 | ||||||
| chr3:124993678
|
C | G | 2 | a0012c0018t0034g0323a0012c0018t0034g0329 | 2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.3653-2692G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993678 | ||||||
| chr3:124993827
|
G | C | 2 | a0008c0012t0013g0227a0008c0012t0013g0228 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3653-2841C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993827 | ||||||
| chr3:124993848
|
T | C | 1 | a0011c0008t0034g0235 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3653-2862A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993848 | ||||||
| chr3:124994074
|
T | G | 1 | a0006c0006t0088g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3653-3088A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994074 | ||||||
| chr3:124994179
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3653-3193G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994179 | ||||||
| chr3:124994496
|
G | T | 110 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(107): Show | 111 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3652+3193C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994496 | ||||||
| chr3:124994507
|
C | CT | 10 | a0002c0049t0087g0028a0003c0004t0002g0089a0004c0033t0023g0163others(7): Show | 11 | HG01346.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3652+3181dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994507 | ||||||
| chr3:124994523
|
G | T | 37 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(34): Show | 38 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.3652+3166C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994523 | ||||||
| chr3:124994529
|
G | A | 1 | a0001c0001t0047g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3652+3160C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994529 | ||||||
| chr3:124994566
|
C | A | 112 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(109): Show | 113 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.3652+3123G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994566 | ||||||
| chr3:124994784
|
G | A | 1 | a0050c0050t0022g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3652+2905C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994784 | ||||||
| chr3:124994839
|
C | A | 85 | a0001c0001t0077g0043a0001c0001t0113g0150a0001c0002t0001g0074others(82): Show | 86 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3652+2850G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994839 | ||||||
| chr3:124995065
|
G | A | 2 | a0016c0029t0007g0035a0041c0069t0111g0203 | 2 | HG01433.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3652+2624C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995065 | ||||||
| chr3:124995441
|
G | A | 1 | a0002c0003t0003g0003 | 2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3652+2248C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995441 | ||||||
| chr3:124995448
|
G | T | 6 | a0001c0001t0070g0194a0004c0081t0116g0246a0004c0082t0069g0190others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3652+2241C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995448 | ||||||
| chr3:124995522
|
A | T | 1 | a0001c0001t0098g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3652+2167T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995522 | ||||||
| chr3:124995552
|
A | G | 1 | a0014c0019t0001g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3652+2137T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995552 | ||||||
| chr3:124995636
|
C | A | 1 | a0014c0019t0114g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3652+2053G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995636 | ||||||
| chr3:124995661
|
C | G | 1 | a0049c0051t0023g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3652+2028G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995661 | ||||||
| chr3:124995718
|
G | A | 6 | a0001c0001t0070g0194a0004c0081t0116g0246a0004c0082t0069g0190others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3652+1971C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995718 | ||||||
| chr3:124995931
|
T | C | 4 | a0001c0002t0001g0091a0001c0002t0024g0092a0001c0002t0024g0093others(1): Show | 4 | HG00140.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652+1758A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995931 | ||||||
| chr3:124996024
|
C | A | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3652+1665G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996024 | ||||||
| chr3:124996038
|
T | C | 6 | a0001c0001t0070g0194a0004c0081t0116g0246a0004c0082t0069g0190others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3652+1651A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996038 | ||||||
| chr3:124996079
|
A | C | 1 | a0059c0057t0128g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3652+1610T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996079 | ||||||
| chr3:124996124
|
C | T | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3652+1565G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996124 | ||||||
| chr3:124996145
|
T | C | 253 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(250): Show | 257 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.3652+1544A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996145 | ||||||
| chr3:124996146
|
G | A | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3652+1543C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996146 | ||||||
| chr3:124996153
|
C | T | 1 | a0003c0067t0019g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3652+1536G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996153 | ||||||
| chr3:124996155
|
G | A | 1 | a0004c0005t0042g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3652+1534C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996155 | ||||||
| chr3:124996156
|
C | A | 1 | a0004c0005t0042g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3652+1533G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996156 | ||||||
| chr3:124996178
|
G | A | 1 | a0001c0002t0016g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3652+1511C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996178 | ||||||
| chr3:124996180
|
G | A | 2 | a0006c0086t0090g0084a0050c0050t0022g0031 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3652+1509C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996180 | ||||||
| chr3:124996188
|
G | A | 41 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(38): Show | 42 | HG00733.hp1 HG01433.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.3652+1501C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996188 | ||||||
| chr3:124996276
|
G | A | 1 | a0011c0008t0034g0235 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3652+1413C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996276 | ||||||
| chr3:124996326
|
T | C | 130 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(127): Show | 133 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3652+1363A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996326 | ||||||
| chr3:124996330
|
C | T | 41 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(38): Show | 42 | HG00733.hp1 HG01433.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.3652+1359G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996330 | ||||||
| chr3:124996364
|
G | T | 121 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(118): Show | 122 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.3652+1325C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996364 | ||||||
| chr3:124996470
|
T | A | 8 | a0007c0011t0022g0002a0007c0011t0086g0080a0007c0077t0073g0087others(5): Show | 10 | HG00735.hp2 HG01074.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3652+1219A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996470 | ||||||
| chr3:124996485
|
C | T | 2 | a0001c0001t0126g0274a0001c0001t0127g0301 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3652+1204G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996485 | ||||||
| chr3:124996648
|
A | G | 8 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193others(5): Show | 8 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3652+1041T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996648 | ||||||
| chr3:124996682
|
T | C | 124 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(121): Show | 126 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.3652+1007A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996682 | ||||||
| chr3:124996852
|
A | G | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3652+837T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996852 | ||||||
| chr3:124997020
|
G | C | 1 | a0001c0001t0012g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3652+669C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997020 | ||||||
| chr3:124997197
|
A | G | 2 | a0012c0018t0056g0352a0057c0061t0035g0223 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3652+492T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997197 | ||||||
| chr3:124997200
|
T | C | 122 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(119): Show | 124 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.3652+489A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997200 | ||||||
| chr3:124997341
|
C | A | 1 | a0001c0085t0132g0289 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3652+348G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997341 | ||||||
| chr3:124997862
|
C | T | 4 | a0005c0007t0013g0307a0005c0007t0013g0314a0005c0007t0025g0308others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3518-39G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124997862 | ||||||
| chr3:124997916
|
T | A | 4 | a0018c0037t0063g0256a0018c0037t0109g0186a0021c0043t0063g0342others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3518-93A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124997916 | ||||||
| chr3:124998045
|
T | C | 128 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(125): Show | 131 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.3518-222A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998045 | ||||||
| chr3:124998127
|
T | G | 1 | a0006c0006t0004g0291 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3518-304A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998127 | ||||||
| chr3:124998213
|
G | A | 50 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(47): Show | 51 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.3518-390C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998213 | ||||||
| chr3:124998226
|
G | A | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3518-403C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998226 | ||||||
| chr3:124998250
|
C | T | 1 | a0003c0004t0021g0168 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3518-427G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998250 | ||||||
| chr3:124998815
|
C | T | 50 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(47): Show | 51 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.3518-992G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998815 | ||||||
| chr3:124998921
|
A | G | 1 | a0003c0004t0021g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3518-1098T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998921 | ||||||
| chr3:124998951
|
C | T | 3 | a0022c0026t0053g0304a0022c0026t0053g0305a0022c0026t0117g0306 | 3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3518-1128G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998951 | ||||||
| chr3:124999021
|
C | T | 1 | a0035c0065t0066g0012 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3518-1198G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999021 | ||||||
| chr3:124999039
|
A | C | 40 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(37): Show | 41 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.3518-1216T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999039 | ||||||
| chr3:124999108
|
C | T | 1 | a0007c0011t0011g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3518-1285G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999108 | ||||||
| chr3:124999224
|
C | T | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3518-1401G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999224 | ||||||
| chr3:124999234
|
C | G | 2 | a0006c0086t0090g0084a0050c0050t0022g0031 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3518-1411G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999234 | ||||||
| chr3:124999525
|
A | G | 130 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(127): Show | 133 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3518-1702T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999525 | ||||||
| chr3:124999718
|
C | T | 5 | a0001c0001t0070g0194a0004c0082t0069g0190a0022c0026t0053g0304others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3518-1895G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999718 | ||||||
| chr3:124999925
|
A | G | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 184 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.3517+1927T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999925 | ||||||
| chr3:124999932
|
G | C | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3517+1920C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999932 | ||||||
| chr3:125000132
|
T | A | 1 | a0001c0002t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3517+1720A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000132 | ||||||
| chr3:125000312
|
G | A | 6 | a0001c0001t0044g0103a0001c0001t0061g0290a0001c0001t0100g0095others(3): Show | 6 | HG01071.hp2 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3517+1540C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000312 | ||||||
| chr3:125000598
|
CT | C | 13 | a0004c0035t0001g0154a0006c0086t0090g0084a0008c0060t0139g0218others(10): Show | 13 | HG01346.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3517+1253delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000598 | ||||||
| chr3:125000609
|
T | C | 1 | a0002c0003t0074g0075 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3517+1243A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000609 | ||||||
| chr3:125000753
|
C | T | 5 | a0029c0047t0108g0018a0030c0058t0057g0220a0030c0059t0058g0221others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3517+1099G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000753 | ||||||
| chr3:125000843
|
T | C | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 184 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.3517+1009A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000843 | ||||||
| chr3:125000893
|
A | G | 3 | a0006c0006t0009g0141a0006c0006t0054g0249a0016c0029t0020g0034 | 3 | HG00323.hp1 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3517+959T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000893 | ||||||
| chr3:125000923
|
C | G | 1 | a0006c0006t0019g0110 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3517+929G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000923 | ||||||
| chr3:125001071
|
C | T | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3517+781G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001071 | ||||||
| chr3:125001234
|
CT | C | 54 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(51): Show | 55 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.3517+617delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001234 | ||||||
| chr3:125001249
|
A | G | 1 | a0002c0003t0003g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3517+603T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001249 | ||||||
| chr3:125001714
|
T | A | 4 | a0018c0037t0063g0256a0018c0037t0109g0186a0021c0043t0063g0342others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3517+138A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001714 | ||||||
| chr3:125001818
|
T | A | 1 | a0002c0003t0015g0083 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3517+34A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001818 | ||||||
| chr3:125002039
|
A | G | 3 | a0007c0077t0073g0087a0020c0025t0025g0008a0020c0025t0130g0318 | 4 | HG00735.hp2 HG01074.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.3357-27T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 10/16 | chr3 | 125002039 | ||||||
| chr3:125002057
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3357-45C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 10/16 | chr3 | 125002057 | ||||||
| chr3:125002084
|
T | C | 1 | a0004c0005t0135g0272 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3357-72A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 10/16 | chr3 | 125002084 | ||||||
| chr3:125002659
|
C | T | 176 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(173): Show | 180 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(177): Show |
intron_variant | MODIFIER | c.3298-344G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002659 | ||||||
| chr3:125002729
|
C | T | 1 | a0003c0004t0009g0195 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3298-414G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002729 | ||||||
| chr3:125002829
|
T | C | 1 | a0004c0033t0094g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3298-514A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002829 | ||||||
| chr3:125002947
|
G | A | 126 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(123): Show | 129 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.3298-632C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002947 | ||||||
| chr3:125003123
|
T | C | 8 | a0002c0003t0046g0117a0005c0007t0013g0338a0005c0007t0060g0334others(5): Show | 8 | HG00597.hp2 HG02083.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.3298-808A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003123 | ||||||
| chr3:125003177
|
C | T | 81 | a0001c0001t0077g0043a0001c0001t0113g0150a0001c0002t0001g0074others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.3298-862G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003177 | ||||||
| chr3:125003266
|
T | C | 2 | a0002c0003t0046g0117a0037c0083t0046g0118 | 2 | NA18991.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3298-951A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003266 | ||||||
| chr3:125003385
|
T | A | 1 | a0002c0003t0002g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3298-1070A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003385 | ||||||
| chr3:125003775
|
T | G | 10 | a0001c0001t0126g0274a0001c0001t0127g0301a0007c0011t0022g0002others(7): Show | 12 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.3298-1460A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003775 | ||||||
| chr3:125003797
|
C | G | 352 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(349): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.3297+1468G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003797 | ||||||
| chr3:125003816
|
C | A | 177 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(174): Show | 181 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.3297+1449G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003816 | ||||||
| chr3:125003843
|
C | T | 6 | a0001c0001t0070g0194a0004c0081t0116g0246a0004c0082t0069g0190others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3297+1422G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003843 | ||||||
| chr3:125003917
|
G | A | 2 | a0001c0002t0001g0127a0033c0063t0005g0239 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3297+1348C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003917 | ||||||
| chr3:125004052
|
G | A | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3297+1213C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004052 | ||||||
| chr3:125004178
|
T | C | 1 | a0050c0050t0022g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3297+1087A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004178 | ||||||
| chr3:125004198
|
C | T | 2 | a0003c0004t0014g0285a0035c0065t0066g0012 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3297+1067G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004198 | ||||||
| chr3:125004294
|
T | C | 40 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(37): Show | 41 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.3297+971A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004294 | ||||||
| chr3:125004351
|
A | G | 12 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3297+914T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004351 | ||||||
| chr3:125004558
|
C | A | 1 | a0027c0032t0065g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3297+707G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004558 | ||||||
| chr3:125004716
|
TA | T | 19 | a0001c0001t0008g0294a0001c0001t0070g0194a0001c0002t0024g0138others(16): Show | 20 | HG01168.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3297+548delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004716 | ||||||
| chr3:125004716
|
TAA | T | 50 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(47): Show | 51 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.3297+547_3297+548d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004716 | ||||||
| chr3:125004746
|
G | A | 4 | a0004c0005t0011g0197a0004c0005t0012g0112a0004c0005t0012g0157others(1): Show | 4 | HG00621.hp1 NA18747.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.3297+519C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004746 | ||||||
| chr3:125004751
|
G | C | 1 | a0013c0040t0028g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3297+514C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004751 | ||||||
| chr3:125004916
|
A | G | 92 | a0001c0001t0077g0043a0001c0001t0113g0150a0001c0002t0001g0074others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.3297+349T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004916 | ||||||
| chr3:125005178
|
A | C | 5 | a0015c0017t0028g0284a0015c0017t0041g0152a0015c0017t0096g0048others(2): Show | 5 | HG00323.hp2 HG01255.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.3297+87T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125005178 | ||||||
| chr3:125005739
|
T | C | 8 | a0006c0086t0090g0084a0019c0023t0031g0182a0019c0023t0031g0192others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3194-371A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005739 | ||||||
| chr3:125005890
|
T | C | 2 | a0006c0006t0002g0178a0009c0009t0138g0348 | 2 | HG00735.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.3194-522A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005890 | ||||||
| chr3:125005979
|
G | A | 125 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(122): Show | 128 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.3194-611C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005979 | ||||||
| chr3:125005990
|
A | C | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-622T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005990 | ||||||
| chr3:125006016
|
G | T | 1 | a0013c0042t0134g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3194-648C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006016 | ||||||
| chr3:125006100
|
A | T | 1 | a0008c0060t0139g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3194-732T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006100 | ||||||
| chr3:125006260
|
C | A | 5 | a0001c0001t0070g0194a0004c0082t0069g0190a0022c0026t0053g0304others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3194-892G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006260 | ||||||
| chr3:125006432
|
G | A | 1 | a0001c0020t0041g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3194-1064C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006432 | ||||||
| chr3:125006452
|
A | G | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-1084T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006452 | ||||||
| chr3:125006691
|
G | A | 1 | a0050c0050t0022g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3194-1323C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006691 | ||||||
| chr3:125006815
|
C | A | 187 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(184): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.3194-1447G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006815 | ||||||
| chr3:125006871
|
G | C | 1 | a0004c0005t0004g0278 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3194-1503C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006871 | ||||||
| chr3:125006938
|
G | A | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-1570C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006938 | ||||||
| chr3:125006943
|
T | C | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-1575A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006943 | ||||||
| chr3:125007026
|
C | T | 1 | a0004c0005t0010g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3194-1658G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007026 | ||||||
| chr3:125007133
|
A | G | 56 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(53): Show | 57 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(54): Show |
intron_variant | MODIFIER | c.3194-1765T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007133 | ||||||
| chr3:125007198
|
C | CA | 73 | a0001c0001t0018g0254a0001c0001t0047g0122a0001c0001t0059g0262others(70): Show | 76 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.3194-1831dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007198 | ||||||
| chr3:125007198
|
C | CAA | 8 | a0004c0081t0116g0246a0005c0038t0131g0303a0007c0077t0073g0087others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3194-1832_3194-183 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007198 | ||||||
| chr3:125007198
|
CA | C | 8 | a0001c0001t0004g0295a0001c0001t0027g0281a0001c0001t0092g0187others(5): Show | 8 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3194-1831delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007198 | ||||||
| chr3:125007455
|
T | C | 8 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193others(5): Show | 8 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3194-2087A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007455 | ||||||
| chr3:125007747
|
A | G | 261 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(258): Show | 265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3193+1958T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007747 | ||||||
| chr3:125007861
|
G | A | 105 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(102): Show | 106 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.3193+1844C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007861 | ||||||
| chr3:125008464
|
A | C | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3193+1241T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008464 | ||||||
| chr3:125008580
|
C | G | 12 | a0001c0001t0126g0274a0001c0001t0127g0301a0007c0011t0022g0002others(9): Show | 14 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3193+1125G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008580 | ||||||
| chr3:125008712
|
G | A | 1 | a0018c0037t0109g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3193+993C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008712 | ||||||
| chr3:125008814
|
AAAAACAC | A | 261 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(258): Show | 265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3193+884_3193+890d others(9): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008814 | ||||||
| chr3:125008821
|
C | A | 1 | a0005c0038t0013g0324 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3193+884G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008821 | ||||||
| chr3:125008903
|
A | G | 205 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.3193+802T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008903 | ||||||
| chr3:125008934
|
C | T | 186 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(183): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.3193+771G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008934 | ||||||
| chr3:125009215
|
T | A | 1 | a0003c0004t0002g0171 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3193+490A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009215 | ||||||
| chr3:125009216
|
A | C | 1 | a0050c0050t0022g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3193+489T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009216 | ||||||
| chr3:125009249
|
A | AATC | 57 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(54): Show | 58 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(55): Show |
intron_variant | MODIFIER | c.3193+453_3193+455d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009249 | ||||||
| chr3:125009286
|
G | GT | 15 | a0001c0002t0016g0046a0001c0002t0033g0050a0005c0007t0125g0346others(12): Show | 17 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3193+418dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009286 | ||||||
| chr3:125009401
|
G | A | 1 | a0001c0002t0016g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3193+304C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009401 | ||||||
| chr3:125009550
|
T | C | 262 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(259): Show | 266 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.3193+155A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009550 | ||||||
| chr3:125009628
|
C | G | 205 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.3193+77G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009628 | ||||||
| chr3:125009671
|
C | T | 1 | a0003c0067t0019g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3193+34G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009671 | ||||||
| chr3:125009964
|
C | A | 55 | a0002c0003t0007g0069a0002c0003t0007g0070a0002c0003t0007g0076others(52): Show | 56 | HG00597.hp2 HG01433.hp2 HG01891.hp2 others(53): Show |
intron_variant | MODIFIER | c.3074-140G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125009964 | ||||||
| chr3:125010048
|
G | T | 1 | a0001c0001t0098g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3074-224C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010048 | ||||||
| chr3:125010067
|
A | G | 2 | a0043c0075t0076g0181a0055c0090t0119g0350 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.3074-243T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010067 | ||||||
| chr3:125010160
|
C | T | 4 | a0012c0041t0035g0310a0012c0041t0035g0312a0042c0079t0079g0180others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3073+279G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010160 | ||||||
| chr3:125010228
|
G | C | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3073+211C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010228 | ||||||
| chr3:125010253
|
G | T | 261 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(258): Show | 264 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.3073+186C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010253 | ||||||
| chr3:125010258
|
G | C | 169 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0012g0172others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.3073+181C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010258 | ||||||
| chr3:125010349
|
T | G | 153 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0012g0172others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.3073+90A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010349 | ||||||
| chr3:125010397
|
G | A | 2 | a0004c0082t0069g0190a0008c0060t0139g0218 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3073+42C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010397 | ||||||
| chr3:125010666
|
T | C | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2957-111A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010666 | ||||||
| chr3:125010680
|
A | T | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2957-125T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010680 | ||||||
| chr3:125010874
|
C | G | 1 | a0006c0006t0022g0088 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2957-319G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010874 | ||||||
| chr3:125010990
|
C | T | 1 | a0001c0002t0005g0298 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2957-435G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010990 | ||||||
| chr3:125011245
|
C | CA | 100 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(97): Show | 104 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2957-691dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011245 | ||||||
| chr3:125011245
|
C | CAA | 11 | a0002c0003t0082g0184a0002c0071t0083g0185a0005c0007t0013g0307others(8): Show | 11 | HG01243.hp1 HG01346.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.2957-692_2957-691d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011245 | ||||||
| chr3:125011245
|
CA | C | 7 | a0001c0001t0059g0262a0001c0002t0024g0115a0006c0006t0022g0088others(4): Show | 7 | HG01891.hp2 HG02148.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2957-691delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011245 | ||||||
| chr3:125011288
|
T | C | 111 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(108): Show | 115 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2957-733A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011288 | ||||||
| chr3:125011408
|
C | T | 5 | a0007c0011t0010g0191a0007c0011t0022g0002a0007c0011t0086g0080others(2): Show | 6 | HG01109.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957-853G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011408 | ||||||
| chr3:125011441
|
A | T | 168 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(165): Show | 169 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.2957-886T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011441 | ||||||
| chr3:125011597
|
G | T | 1 | a0013c0040t0059g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2956+1026C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011597 | ||||||
| chr3:125011715
|
G | T | 1 | a0002c0071t0083g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2956+908C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011715 | ||||||
| chr3:125011770
|
C | T | 1 | a0001c0001t0027g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2956+853G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011770 | ||||||
| chr3:125012081
|
C | G | 176 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2956+542G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012081 | ||||||
| chr3:125012095
|
C | T | 1 | a0009c0009t0004g0330 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2956+528G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012095 | ||||||
| chr3:125012129
|
C | T | 1 | a0004c0028t0080g0027 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2956+494G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012129 | ||||||
| chr3:125012228
|
T | A | 296 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(293): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2956+395A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012228 | ||||||
| chr3:125012237
|
TCTTTA | T | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2956+381_2956+385d others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012237 | ||||||
| chr3:125013998
|
C | A | 272 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(269): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
splice_region_variant&intron_variant | LOW | c.1589-8G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125013998 | ||||||
| chr3:125014018
|
C | G | 7 | a0018c0037t0063g0256a0018c0037t0109g0186a0018c0088t0010g0177others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1589-28G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014018 | ||||||
| chr3:125014132
|
G | T | 282 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(279): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1589-142C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014132 | ||||||
| chr3:125014133
|
G | T | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1589-143C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014133 | ||||||
| chr3:125014153
|
ACAT | A | 3 | a0022c0026t0053g0304a0022c0026t0053g0305a0022c0026t0117g0306 | 3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1589-166_1589-164d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014153 | ||||||
| chr3:125014377
|
T | C | 1 | a0004c0005t0043g0147 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1589-387A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014377 | ||||||
| chr3:125014510
|
G | A | 2 | a0043c0075t0076g0181a0055c0090t0119g0350 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1589-520C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014510 | ||||||
| chr3:125014512
|
G | A | 1 | a0001c0001t0099g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1589-522C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014512 | ||||||
| chr3:125014523
|
G | C | 2 | a0004c0082t0069g0190a0008c0060t0139g0218 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1589-533C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014523 | ||||||
| chr3:125014641
|
T | A | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-651A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014641 | ||||||
| chr3:125014650
|
G | T | 339 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(336): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1589-660C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014650 | ||||||
| chr3:125014655
|
G | A | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1589-665C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014655 | ||||||
| chr3:125014682
|
G | A | 2 | a0013c0042t0004g0349a0013c0042t0134g0345 | 2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1589-692C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014682 | ||||||
| chr3:125014769
|
A | C | 1 | a0002c0003t0006g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1589-779T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014769 | ||||||
| chr3:125014805
|
T | G | 296 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(293): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1589-815A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014805 | ||||||
| chr3:125014927
|
G | C | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1589-937C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014927 | ||||||
| chr3:125015024
|
G | A | 3 | a0012c0041t0035g0310a0012c0041t0035g0312a0054c0091t0122g0311 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1589-1034C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015024 | ||||||
| chr3:125015108
|
C | T | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1589-1118G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015108 | ||||||
| chr3:125015482
|
C | T | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1589-1492G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015482 | ||||||
| chr3:125015609
|
C | T | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1589-1619G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015609 | ||||||
| chr3:125015649
|
T | G | 3 | a0001c0001t0059g0262a0006c0006t0088g0065a0047c0080t0085g0086 | 3 | HG01891.hp2 HG02148.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1589-1659A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015649 | ||||||
| chr3:125015702
|
T | A | 4 | a0020c0025t0025g0008a0020c0025t0130g0318a0043c0075t0076g0181others(1): Show | 5 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589-1712A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015702 | ||||||
| chr3:125015733
|
T | C | 1 | a0002c0003t0015g0071 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1589-1743A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015733 | ||||||
| chr3:125015792
|
A | G | 4 | a0001c0002t0001g0091a0001c0002t0024g0092a0001c0002t0024g0093others(1): Show | 4 | HG00140.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589-1802T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015792 | ||||||
| chr3:125015801
|
C | A | 190 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1589-1811G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015801 | ||||||
| chr3:125015802
|
C | A | 164 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1589-1812G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015802 | ||||||
| chr3:125015966
|
C | T | 290 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1589-1976G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015966 | ||||||
| chr3:125015979
|
T | C | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1589-1989A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015979 | ||||||
| chr3:125015980
|
C | A | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1589-1990G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015980 | ||||||
| chr3:125016091
|
T | C | 4 | a0001c0001t0059g0262a0006c0006t0022g0088a0006c0006t0088g0065others(1): Show | 4 | HG01891.hp2 HG02148.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1589-2101A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016091 | ||||||
| chr3:125016314
|
A | C | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1589-2324T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016314 | ||||||
| chr3:125016438
|
C | T | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-2448G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016438 | ||||||
| chr3:125016471
|
G | A | 4 | a0011c0008t0004g0238a0011c0008t0036g0240a0011c0008t0036g0241others(1): Show | 4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589-2481C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016471 | ||||||
| chr3:125016625
|
C | T | 9 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0093g0162others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1589-2635G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016625 | ||||||
| chr3:125016627
|
T | C | 190 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1588+2635A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016627 | ||||||
| chr3:125016628
|
G | A | 10 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193others(7): Show | 10 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588+2634C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016628 | ||||||
| chr3:125016787
|
T | C | 3 | a0004c0033t0023g0163a0004c0044t0023g0015a0013c0089t0026g0313 | 3 | HG03195.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1588+2475A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016787 | ||||||
| chr3:125016788
|
G | A | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1588+2474C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016788 | ||||||
| chr3:125017059
|
CT | C | 214 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1588+2202delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017059 | ||||||
| chr3:125017120
|
T | A | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1588+2142A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017120 | ||||||
| chr3:125017141
|
A | G | 290 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1588+2121T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017141 | ||||||
| chr3:125017201
|
C | T | 1 | a0001c0002t0051g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1588+2061G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017201 | ||||||
| chr3:125017301
|
C | T | 7 | a0018c0037t0063g0256a0018c0037t0109g0186a0018c0088t0010g0177others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1961G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017301 | ||||||
| chr3:125017406
|
T | C | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1856A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017406 | ||||||
| chr3:125017529
|
C | T | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1588+1733G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017529 | ||||||
| chr3:125017530
|
C | T | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1732G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017530 | ||||||
| chr3:125017534
|
C | T | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1728G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017534 | ||||||
| chr3:125017661
|
C | T | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1601G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017661 | ||||||
| chr3:125017747
|
A | G | 278 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(275): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1588+1515T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017747 | ||||||
| chr3:125017864
|
T | TA | 25 | a0001c0001t0007g0113a0001c0002t0001g0074a0001c0002t0001g0079others(22): Show | 25 | HG00099.hp2 HG01167.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1588+1397dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017864 | ||||||
| chr3:125017946
|
G | A | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1316C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017946 | ||||||
| chr3:125018010
|
C | T | 2 | a0001c0002t0016g0046a0001c0002t0033g0045 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1588+1252G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018010 | ||||||
| chr3:125018028
|
C | CA | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1233dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018028 | ||||||
| chr3:125018037
|
A | T | 75 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(72): Show | 78 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1588+1225T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018037 | ||||||
| chr3:125018042
|
T | A | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1588+1220A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018042 | ||||||
| chr3:125018142
|
A | T | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1588+1120T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018142 | ||||||
| chr3:125018195
|
T | C | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1067A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018195 | ||||||
| chr3:125018282
|
T | C | 3 | a0012c0041t0035g0310a0012c0041t0035g0312a0054c0091t0122g0311 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1588+980A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018282 | ||||||
| chr3:125018454
|
C | T | 1 | a0013c0040t0059g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1588+808G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018454 | ||||||
| chr3:125018585
|
C | T | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1588+677G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018585 | ||||||
| chr3:125018820
|
G | C | 2 | a0001c0002t0001g0127a0033c0063t0005g0239 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1588+442C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018820 | ||||||
| chr3:125018864
|
C | CT | 15 | a0001c0001t0018g0254a0001c0002t0001g0142a0002c0003t0006g0267others(12): Show | 15 | HG00639.hp1 HG01255.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1588+397dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018864 | ||||||
| chr3:125018864
|
CT | C | 18 | a0001c0001t0004g0276a0002c0071t0083g0185a0004c0005t0012g0157others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1588+397delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018864 | ||||||
| chr3:125018959
|
T | C | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1588+303A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018959 | ||||||
| chr3:125018968
|
A | C | 3 | a0022c0026t0053g0304a0022c0026t0053g0305a0022c0026t0117g0306 | 3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1588+294T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018968 | ||||||
| chr3:125019040
|
G | A | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1588+222C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019040 | ||||||
| chr3:125019049
|
G | T | 1 | a0010c0022t0008g0233 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1588+213C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019049 | ||||||
| chr3:125019069
|
T | C | 4 | a0001c0002t0016g0051a0001c0002t0033g0050a0010c0016t0141g0224others(1): Show | 4 | NA18955.hp2 NA18989.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1588+193A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019069 | ||||||
| chr3:125019187
|
C | T | 2 | a0001c0001t0097g0144a0007c0015t0005g0287 | 2 | HG00597.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1588+75G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019187 | ||||||
| chr3:125019205
|
C | A | 1 | a0002c0003t0006g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1588+57G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019205 | ||||||
| chr3:125019228
|
A | G | 1 | a0001c0002t0005g0288 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1588+34T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019228 | ||||||
| chr3:125019860
|
C | T | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1253-263G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125019860 | ||||||
| chr3:125020020
|
A | G | 7 | a0007c0077t0073g0087a0012c0041t0035g0310a0012c0041t0035g0312others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1253-423T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020020 | ||||||
| chr3:125020074
|
T | A | 1 | a0001c0002t0033g0050 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1253-477A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020074 | ||||||
| chr3:125020164
|
T | C | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253-567A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020164 | ||||||
| chr3:125020290
|
G | C | 172 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1252+502C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020290 | ||||||
| chr3:125020775
|
A | G | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1252+17T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020775 | ||||||
| chr3:125021160
|
T | A | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-30A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021160 | ||||||
| chr3:125021611
|
G | A | 189 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.914-481C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021611 | ||||||
| chr3:125021694
|
G | C | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.914-564C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021694 | ||||||
| chr3:125021960
|
T | C | 1 | a0015c0017t0045g0131 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.914-830A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021960 | ||||||
| chr3:125022010
|
C | T | 2 | a0006c0006t0022g0088a0040c0078t0015g0155 | 2 | HG03098.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.914-880G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022010 | ||||||
| chr3:125022015
|
T | C | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-885A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022015 | ||||||
| chr3:125022049
|
C | T | 1 | a0001c0002t0001g0132 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.914-919G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022049 | ||||||
| chr3:125022227
|
G | A | 87 | a0001c0001t0007g0113a0001c0001t0044g0160a0001c0001t0097g0144others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.914-1097C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022227 | ||||||
| chr3:125022396
|
C | CGA | 23 | a0001c0001t0047g0122a0001c0002t0033g0050a0002c0003t0082g0184others(20): Show | 23 | HG00140.hp2 HG01346.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.914-1268_914-1267d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
C | CGAGA | 138 | a0001c0001t0006g0283a0001c0001t0007g0113a0001c0001t0008g0244others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.914-1270_914-1267d others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
C | CGAGAGA | 31 | a0001c0001t0006g0282a0001c0001t0018g0253a0001c0001t0042g0097others(28): Show | 31 | HG00323.hp2 HG00609.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.914-1272_914-1267d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
C | CGAGAGAG others(1): Show |
8 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0279others(5): Show | 8 | HG01255.hp1 HG03139.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-1274_914-1267d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
C | CGAGAGAG others(3): Show |
5 | a0001c0001t0004g0277a0029c0046t0019g0029a0030c0059t0058g0221others(2): Show | 5 | HG00639.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-1276_914-1267d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
C | CGAGAGAG others(5): Show |
1 | a0029c0047t0108g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.914-1278_914-1267d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
C | CGAGAGAG others(7): Show |
2 | a0030c0058t0057g0220a0034c0066t0068g0010 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.914-1280_914-1267d others(16): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022396
|
CGA | C | 4 | a0022c0026t0053g0304a0022c0026t0053g0305a0022c0026t0117g0306others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-1268_914-1267d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | ||||||
| chr3:125022428
|
T | A | 189 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.914-1298A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022428 | ||||||
| chr3:125022454
|
C | G | 2 | a0001c0002t0016g0046a0001c0002t0033g0045 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.914-1324G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022454 | ||||||
| chr3:125022554
|
A | G | 1 | a0019c0023t0031g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.914-1424T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022554 | ||||||
| chr3:125022612
|
G | A | 76 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(73): Show | 79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.914-1482C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022612 | ||||||
| chr3:125022653
|
T | C | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.914-1523A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022653 | ||||||
| chr3:125022693
|
AAAGAAAT | A | 16 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(13): Show | 16 | HG00323.hp1 HG00735.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.914-1570_914-1564d others(9): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022693 | ||||||
| chr3:125022694
|
AAGAAAT | A | 156 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0007g0113others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.914-1570_914-1565d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022694 | ||||||
| chr3:125022694
|
AAGAAATA others(3): Show |
A | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-1574_914-1565d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022694 | ||||||
| chr3:125022704
|
T | G | 172 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.914-1574A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022704 | ||||||
| chr3:125022707
|
AT | A | 4 | a0001c0010t0001g0022a0010c0016t0005g0222a0028c0036t0030g0067others(1): Show | 4 | HG02083.hp2 HG02132.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-1578delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022707 | ||||||
| chr3:125022708
|
T | G | 175 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.914-1578A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022708 | ||||||
| chr3:125022709
|
A | G | 4 | a0001c0010t0001g0022a0010c0016t0005g0222a0028c0036t0030g0067others(1): Show | 4 | HG02083.hp2 HG02132.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-1579T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022709 | ||||||
| chr3:125022713
|
AG | A | 175 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.914-1584delC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022713 | ||||||
| chr3:125022876
|
T | G | 1 | a0001c0001t0127g0301 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.914-1746A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022876 | ||||||
| chr3:125022915
|
C | T | 1 | a0014c0019t0001g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.914-1785G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022915 | ||||||
| chr3:125023051
|
G | A | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-1921C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023051 | ||||||
| chr3:125023079
|
A | G | 1 | a0015c0017t0045g0131 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.914-1949T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023079 | ||||||
| chr3:125023125
|
T | C | 2 | a0038c0084t0019g0085a0057c0061t0035g0223 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.914-1995A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023125 | ||||||
| chr3:125023158
|
T | C | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.914-2028A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023158 | ||||||
| chr3:125023238
|
C | CA | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.914-2109dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023238 | ||||||
| chr3:125023479
|
A | G | 1 | a0002c0003t0006g0286 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.914-2349T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023479 | ||||||
| chr3:125023510
|
G | A | 278 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(275): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.914-2380C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023510 | ||||||
| chr3:125023665
|
T | TA | 189 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.914-2536_914-2535i others(3): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023665 | ||||||
| chr3:125023746
|
C | T | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.914-2616G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023746 | ||||||
| chr3:125023766
|
C | T | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.914-2636G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023766 | ||||||
| chr3:125023972
|
C | CTGA | 189 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.914-2843_914-2842i others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023972 | ||||||
| chr3:125024041
|
A | G | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-2911T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024041 | ||||||
| chr3:125024124
|
T | C | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.914-2994A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024124 | ||||||
| chr3:125024135
|
T | A | 2 | a0004c0082t0069g0190a0008c0060t0139g0218 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.914-3005A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024135 | ||||||
| chr3:125024179
|
T | A | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.913+3026A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024179 | ||||||
| chr3:125024626
|
C | G | 172 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.913+2579G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024626 | ||||||
| chr3:125024729
|
G | A | 2 | a0006c0006t0003g0111a0006c0006t0019g0110 | 2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.913+2476C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024729 | ||||||
| chr3:125024759
|
G | A | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.913+2446C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024759 | ||||||
| chr3:125024868
|
C | T | 182 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.913+2337G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024868 | ||||||
| chr3:125024869
|
T | C | 182 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.913+2336A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024869 | ||||||
| chr3:125024944
|
G | A | 1 | a0005c0007t0129g0347 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.913+2261C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024944 | ||||||
| chr3:125025119
|
G | A | 7 | a0018c0037t0063g0256a0018c0037t0109g0186a0018c0088t0010g0177others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+2086C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025119 | ||||||
| chr3:125025200
|
C | A | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.913+2005G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025200 | ||||||
| chr3:125025450
|
G | A | 4 | a0004c0033t0023g0163a0004c0033t0094g0164a0004c0044t0023g0015others(1): Show | 4 | HG03195.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+1755C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025450 | ||||||
| chr3:125025494
|
A | G | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.913+1711T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025494 | ||||||
| chr3:125025561
|
C | G | 276 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(273): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.913+1644G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025561 | ||||||
| chr3:125025764
|
C | T | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+1441G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025764 | ||||||
| chr3:125025839
|
C | A | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.913+1366G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025839 | ||||||
| chr3:125025922
|
G | C | 3 | a0022c0026t0053g0304a0022c0026t0053g0305a0022c0026t0117g0306 | 3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.913+1283C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025922 | ||||||
| chr3:125026198
|
T | G | 5 | a0007c0011t0010g0191a0007c0011t0022g0002a0007c0011t0086g0080others(2): Show | 6 | HG01109.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.913+1007A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026198 | ||||||
| chr3:125026287
|
C | T | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.913+918G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026287 | ||||||
| chr3:125026627
|
A | G | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.913+578T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026627 | ||||||
| chr3:125026874
|
C | T | 1 | a0059c0057t0128g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.913+331G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026874 | ||||||
| chr3:125026937
|
T | C | 1 | a0001c0001t0077g0043 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.913+268A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026937 | ||||||
| chr3:125027030
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.913+175A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125027030 | ||||||
| chr3:125027538
|
A | G | 1 | a0001c0002t0016g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.611-31T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027538 | ||||||
| chr3:125027737
|
C | A | 2 | a0043c0075t0076g0181a0055c0090t0119g0350 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.611-230G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027737 | ||||||
| chr3:125027836
|
C | A | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.611-329G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027836 | ||||||
| chr3:125027930
|
T | C | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.611-423A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027930 | ||||||
| chr3:125028024
|
TCTGACGG others(69): Show |
T | 1 | a0004c0005t0009g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-593_611-518del others(76): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028024 | ||||||
| chr3:125028214
|
G | A | 1 | a0001c0010t0107g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.611-707C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028214 | ||||||
| chr3:125028338
|
G | A | 13 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.611-831C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028338 | ||||||
| chr3:125028435
|
C | A | 13 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+760G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028435 | ||||||
| chr3:125028517
|
C | A | 3 | a0004c0005t0027g0260a0004c0005t0028g0259a0004c0005t0028g0261 | 3 | NA18999.hp2 NA19062.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.610+678G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028517 | ||||||
| chr3:125028524
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.610+671G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028524 | ||||||
| chr3:125029173
|
C | T | 1 | a0002c0003t0007g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.610+22G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125029173 | ||||||
| chr3:125029653
|
G | T | 1 | a0019c0023t0031g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.317-165C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029653 | ||||||
| chr3:125029708
|
G | A | 1 | a0001c0001t0101g0121 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.317-220C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029708 | ||||||
| chr3:125029749
|
G | A | 1 | a0009c0009t0061g0321 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.317-261C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029749 | ||||||
| chr3:125029792
|
T | C | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-304A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029792 | ||||||
| chr3:125029835
|
T | C | 1 | a0004c0005t0042g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.317-347A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029835 | ||||||
| chr3:125029846
|
C | T | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.317-358G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029846 | ||||||
| chr3:125029865
|
C | A | 1 | a0004c0005t0004g0278 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.317-377G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029865 | ||||||
| chr3:125029945
|
T | G | 3 | a0012c0041t0035g0310a0012c0041t0035g0312a0054c0091t0122g0311 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.317-457A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029945 | ||||||
| chr3:125030115
|
T | C | 1 | a0015c0017t0045g0131 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.317-627A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030115 | ||||||
| chr3:125030201
|
T | C | 1 | a0006c0006t0118g0297 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.317-713A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030201 | ||||||
| chr3:125030432
|
G | A | 190 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.317-944C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030432 | ||||||
| chr3:125030522
|
A | T | 5 | a0003c0004t0014g0285a0003c0004t0040g0174a0003c0004t0040g0175others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-1034T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030522 | ||||||
| chr3:125030619
|
G | GA | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-1132dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030619 | ||||||
| chr3:125030647
|
T | C | 60 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(57): Show | 61 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.317-1159A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030647 | ||||||
| chr3:125030712
|
C | T | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-1224G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030712 | ||||||
| chr3:125030740
|
T | C | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-1252A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030740 | ||||||
| chr3:125030956
|
C | T | 191 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.317-1468G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030956 | ||||||
| chr3:125031127
|
G | A | 275 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.317-1639C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031127 | ||||||
| chr3:125031160
|
G | A | 2 | a0043c0075t0076g0181a0055c0090t0119g0350 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.317-1672C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031160 | ||||||
| chr3:125031164
|
C | T | 9 | a0007c0011t0011g0060a0007c0011t0011g0124a0011c0008t0004g0238others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.317-1676G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031164 | ||||||
| chr3:125031182
|
C | T | 2 | a0006c0006t0022g0088a0042c0079t0079g0180 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-1694G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031182 | ||||||
| chr3:125031306
|
G | T | 13 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.317-1818C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031306 | ||||||
| chr3:125031531
|
C | A | 8 | a0002c0003t0003g0003a0002c0003t0003g0004a0002c0003t0003g0005others(5): Show | 11 | HG00544.hp2 HG00673.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.317-2043G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031531 | ||||||
| chr3:125031572
|
G | T | 11 | a0002c0003t0082g0184a0002c0071t0083g0185a0005c0007t0013g0307others(8): Show | 11 | HG01243.hp1 HG01346.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.317-2084C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031572 | ||||||
| chr3:125031653
|
CCA | C | 7 | a0006c0006t0022g0088a0019c0023t0031g0182a0019c0023t0031g0192others(4): Show | 7 | HG02486.hp2 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-2167_317-2166d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031653 | ||||||
| chr3:125031680
|
TAC | T | 76 | a0001c0010t0001g0013a0002c0003t0002g0156a0002c0003t0003g0003others(73): Show | 79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.317-2194_317-2193d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031680 | ||||||
| chr3:125031687
|
A | C | 4 | a0006c0006t0022g0088a0038c0084t0019g0085a0042c0079t0079g0180others(1): Show | 4 | HG02486.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-2199T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031687 | ||||||
| chr3:125031703
|
A | AC | 7 | a0006c0006t0022g0088a0019c0023t0031g0182a0019c0023t0031g0192others(4): Show | 7 | HG02486.hp2 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-2216dupG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031703 | ||||||
| chr3:125031703
|
AC | A | 174 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.317-2216delG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031703 | ||||||
| chr3:125031710
|
A | C | 3 | a0006c0006t0022g0088a0007c0077t0073g0087a0042c0079t0079g0180 | 3 | HG02572.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-2222T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031710 | ||||||
| chr3:125031830
|
A | G | 178 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.317-2342T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031830 | ||||||
| chr3:125031832
|
G | A | 178 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.317-2344C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031832 | ||||||
| chr3:125031849
|
C | T | 2 | a0038c0084t0019g0085a0057c0061t0035g0223 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-2361G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031849 | ||||||
| chr3:125032137
|
C | A | 2 | a0001c0001t0044g0103a0001c0001t0100g0095 | 2 | HG01243.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.317-2649G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032137 | ||||||
| chr3:125032137
|
C | T | 2 | a0038c0084t0019g0085a0057c0061t0035g0223 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-2649G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032137 | ||||||
| chr3:125032153
|
G | A | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-2665C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032153 | ||||||
| chr3:125032421
|
G | A | 1 | a0040c0078t0015g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.317-2933C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032421 | ||||||
| chr3:125032484
|
C | T | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-2996G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032484 | ||||||
| chr3:125032808
|
C | T | 2 | a0001c0002t0016g0061a0001c0010t0001g0024 | 2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.317-3320G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032808 | ||||||
| chr3:125032868
|
C | A | 2 | a0002c0003t0089g0125a0008c0013t0004g0212 | 2 | NA18974.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.317-3380G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032868 | ||||||
| chr3:125032966
|
G | A | 4 | a0011c0008t0004g0238a0011c0008t0036g0240a0011c0008t0036g0241others(1): Show | 4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-3478C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032966 | ||||||
| chr3:125033014
|
G | A | 1 | a0004c0005t0009g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.317-3526C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033014 | ||||||
| chr3:125033160
|
A | T | 1 | a0001c0001t0101g0121 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.317-3672T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033160 | ||||||
| chr3:125033226
|
G | A | 1 | a0021c0096t0006g0343 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.317-3738C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033226 | ||||||
| chr3:125033293
|
T | C | 1 | a0008c0013t0124g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.317-3805A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033293 | ||||||
| chr3:125033304
|
T | A | 2 | a0006c0006t0022g0088a0042c0079t0079g0180 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-3816A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033304 | ||||||
| chr3:125033734
|
G | A | 6 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-4246C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033734 | ||||||
| chr3:125033777
|
G | A | 2 | a0002c0003t0003g0005a0002c0003t0003g0106 | 3 | NA18944.hp2 NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.317-4289C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033777 | ||||||
| chr3:125033834
|
G | A | 1 | a0003c0004t0021g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.317-4346C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033834 | ||||||
| chr3:125033892
|
GC | G | 3 | a0001c0002t0001g0074a0001c0002t0001g0079a0010c0016t0038g0219 | 3 | NA18942.hp2 NA18970.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.317-4405delG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033892 | ||||||
| chr3:125033899
|
C | G | 4 | a0006c0006t0022g0088a0038c0084t0019g0085a0042c0079t0079g0180others(1): Show | 4 | HG02486.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-4411G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033899 | ||||||
| chr3:125033910
|
T | A | 176 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.317-4422A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033910 | ||||||
| chr3:125033953
|
C | T | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.317-4465G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033953 | ||||||
| chr3:125033961
|
C | T | 1 | a0001c0001t0011g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.317-4473G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033961 | ||||||
| chr3:125033972
|
C | T | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-4484G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033972 | ||||||
| chr3:125034027
|
G | A | 88 | a0001c0002t0016g0061a0001c0010t0001g0013a0001c0010t0001g0024others(85): Show | 92 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.317-4539C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034027 | ||||||
| chr3:125034082
|
T | C | 179 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-4594A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034082 | ||||||
| chr3:125034083
|
G | C | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.317-4595C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034083 | ||||||
| chr3:125034084
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.317-4596C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034084 | ||||||
| chr3:125034094
|
G | A | 1 | a0009c0009t0011g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.317-4606C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034094 | ||||||
| chr3:125034136
|
C | T | 1 | a0019c0023t0031g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.317-4648G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034136 | ||||||
| chr3:125034172
|
A | C | 1 | a0002c0003t0007g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.317-4684T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034172 | ||||||
| chr3:125034184
|
A | G | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-4696T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034184 | ||||||
| chr3:125034192
|
T | TTGATAAC others(43): Show |
180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-4705_317-4704i others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034192 | ||||||
| chr3:125034250
|
T | C | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-4762A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034250 | ||||||
| chr3:125034349
|
T | C | 184 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.317-4861A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034349 | ||||||
| chr3:125034362
|
A | T | 2 | a0038c0084t0019g0085a0057c0061t0035g0223 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-4874T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034362 | ||||||
| chr3:125034363
|
T | A | 1 | a0006c0006t0009g0141 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.317-4875A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034363 | ||||||
| chr3:125034428
|
A | G | 2 | a0038c0084t0019g0085a0057c0061t0035g0223 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-4940T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034428 | ||||||
| chr3:125034433
|
TA | T | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-4946delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034433 | ||||||
| chr3:125034470
|
A | G | 184 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.317-4982T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034470 | ||||||
| chr3:125034538
|
C | T | 2 | a0004c0082t0069g0190a0008c0060t0139g0218 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.317-5050G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034538 | ||||||
| chr3:125034676
|
G | A | 3 | a0009c0009t0018g0339a0038c0084t0019g0085a0057c0061t0035g0223 | 3 | HG02486.hp2 HG03471.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.317-5188C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034676 | ||||||
| chr3:125034690
|
C | T | 5 | a0029c0046t0019g0029a0029c0047t0108g0018a0030c0058t0057g0220others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-5202G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034690 | ||||||
| chr3:125034692
|
T | C | 1 | a0003c0067t0019g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.317-5204A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034692 | ||||||
| chr3:125034922
|
T | C | 4 | a0003c0004t0009g0072a0023c0021t0006g0216a0023c0021t0006g0217others(1): Show | 4 | NA18988.hp2 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-5434A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034922 | ||||||
| chr3:125034977
|
T | C | 2 | a0006c0006t0022g0088a0042c0079t0079g0180 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-5489A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034977 | ||||||
| chr3:125035081
|
C | G | 3 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218 | 3 | HG01891.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.317-5593G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035081 | ||||||
| chr3:125035099
|
A | G | 275 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.317-5611T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035099 | ||||||
| chr3:125035250
|
T | G | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5762A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035250 | ||||||
| chr3:125035251
|
A | C | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5763T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035251 | ||||||
| chr3:125035252
|
A | T | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5764T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035252 | ||||||
| chr3:125035255
|
T | C | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5767A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035255 | ||||||
| chr3:125035256
|
T | A | 1 | a0056c0092t0133g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5768A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035256 | ||||||
| chr3:125035268
|
T | TG | 91 | a0001c0001t0007g0113a0001c0001t0044g0160a0001c0001t0097g0144others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.317-5781dupC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035268 | ||||||
| chr3:125035318
|
G | T | 180 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.317-5830C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035318 | ||||||
| chr3:125035421
|
A | G | 1 | a0005c0007t0025g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.317-5933T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035421 | ||||||
| chr3:125035464
|
A | T | 1 | a0025c0030t0048g0036 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.317-5976T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035464 | ||||||
| chr3:125035580
|
C | T | 1 | a0004c0033t0023g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.317-6092G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035580 | ||||||
| chr3:125035596
|
C | T | 2 | a0002c0003t0007g0082a0002c0003t0015g0083 | 2 | HG03654.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.317-6108G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035596 | ||||||
| chr3:125035729
|
T | A | 3 | a0006c0006t0002g0178a0006c0006t0054g0249a0009c0009t0138g0348 | 3 | HG00323.hp1 HG00735.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.317-6241A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035729 | ||||||
| chr3:125035807
|
G | A | 1 | a0014c0019t0001g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.317-6319C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035807 | ||||||
| chr3:125036209
|
C | CAAAAAA | 48 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0059g0262others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.317-6727_317-6722d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036209
|
C | CAAAAAAA | 124 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.317-6728_317-6722d others(9): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036209
|
C | CAAAAAAA others(1): Show |
6 | a0001c0002t0001g0091a0001c0002t0001g0142a0001c0002t0001g0143others(3): Show | 6 | HG00733.hp1 HG02155.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-6729_317-6722d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036209
|
C | CAAAAAAA others(4): Show |
1 | a0005c0007t0123g0351 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.317-6732_317-6722d others(13): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036209
|
C | CAAAAAAA others(5): Show |
76 | a0001c0002t0016g0061a0001c0010t0001g0013a0001c0010t0001g0024others(73): Show | 79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.317-6733_317-6722d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036209
|
C | CAAAAAAA others(6): Show |
9 | a0002c0049t0087g0028a0004c0005t0004g0278a0004c0005t0027g0260others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-6734_317-6722d others(15): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036209
|
C | CAAAAAAA others(7): Show |
1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.317-6735_317-6722d others(16): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | ||||||
| chr3:125036213
|
A | AAAAAAAA others(5): Show |
3 | a0020c0025t0025g0008a0020c0025t0130g0318a0041c0069t0111g0203 | 4 | HG00735.hp2 HG01074.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-6726_317-6725i others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036213 | ||||||
| chr3:125036299
|
C | T | 6 | a0001c0001t0008g0244a0001c0001t0008g0248a0001c0001t0029g0153others(3): Show | 6 | HG00639.hp2 HG01081.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-6811G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036299 | ||||||
| chr3:125036326
|
A | T | 1 | a0026c0053t0001g0033 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.317-6838T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036326 | ||||||
| chr3:125036381
|
C | T | 76 | a0001c0002t0016g0061a0001c0010t0001g0013a0001c0010t0001g0024others(73): Show | 79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.317-6893G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036381 | ||||||
| chr3:125036391
|
C | T | 1 | a0004c0028t0080g0027 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.317-6903G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036391 | ||||||
| chr3:125036604
|
A | G | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-7116T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036604 | ||||||
| chr3:125036642
|
T | C | 182 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.317-7154A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036642 | ||||||
| chr3:125036832
|
T | C | 2 | a0038c0084t0019g0085a0057c0061t0035g0223 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-7344A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036832 | ||||||
| chr3:125036854
|
T | C | 3 | a0001c0001t0044g0103a0001c0001t0100g0095a0009c0009t0138g0348 | 3 | HG01243.hp2 HG01256.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.317-7366A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036854 | ||||||
| chr3:125036950
|
A | G | 7 | a0004c0081t0116g0246a0004c0082t0069g0190a0008c0060t0139g0218others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-7462T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036950 | ||||||
| chr3:125036979
|
G | A | 1 | a0041c0069t0111g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.317-7491C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036979 | ||||||
| chr3:125036979
|
G | T | 177 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.317-7491C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036979 | ||||||
| chr3:125037125
|
T | C | 1 | a0007c0015t0050g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.317-7637A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037125 | ||||||
| chr3:125037150
|
C | T | 3 | a0019c0023t0031g0182a0019c0023t0031g0192a0019c0023t0031g0193 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-7662G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037150 | ||||||
| chr3:125037175
|
T | C | 19 | a0003c0004t0020g0062a0003c0004t0025g0273a0003c0067t0019g0063others(16): Show | 19 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.317-7687A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037175 | ||||||
| chr3:125037455
|
T | C | 3 | a0008c0060t0139g0218a0013c0089t0026g0313a0027c0032t0026g0243 | 3 | HG02723.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.317-7967A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037455 | ||||||
| chr3:125037546
|
A | T | 28 | a0002c0003t0007g0148a0003c0004t0020g0062a0003c0004t0025g0273others(25): Show | 28 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.317-8058T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037546 | ||||||
| chr3:125037745
|
C | T | 5 | a0003c0004t0020g0062a0007c0015t0050g0064a0012c0018t0034g0323others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-8257G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037745 | ||||||
| chr3:125037823
|
G | C | 44 | a0002c0003t0002g0156a0002c0003t0003g0003a0002c0003t0003g0004others(41): Show | 47 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.317-8335C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037823 | ||||||
| chr3:125037867
|
G | C | 6 | a0006c0086t0090g0084a0007c0076t0091g0161a0018c0037t0063g0256others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-8379C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037867 | ||||||
| chr3:125037888
|
T | C | 1 | a0001c0001t0097g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.317-8400A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037888 | ||||||
| chr3:125037927
|
C | T | 172 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(169): Show | 174 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.317-8439G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037927 | ||||||
| chr3:125037934
|
C | T | 1 | a0001c0001t0059g0262 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.317-8446G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037934 | ||||||
| chr3:125038023
|
T | C | 1 | a0004c0005t0043g0147 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.317-8535A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038023 | ||||||
| chr3:125038051
|
A | G | 102 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(99): Show | 103 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.317-8563T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038051 | ||||||
| chr3:125038409
|
C | T | 1 | a0042c0079t0079g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.317-8921G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038409 | ||||||
| chr3:125038474
|
T | C | 294 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(291): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.317-8986A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038474 | ||||||
| chr3:125038517
|
G | A | 2 | a0001c0001t0044g0103a0001c0001t0100g0095 | 2 | HG01243.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.317-9029C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038517 | ||||||
| chr3:125038572
|
C | A | 1 | a0001c0001t0059g0262 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.317-9084G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038572 | ||||||
| chr3:125038757
|
G | A | 1 | a0008c0013t0058g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.317-9269C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038757 | ||||||
| chr3:125038858
|
A | G | 3 | a0001c0002t0051g0136a0001c0002t0051g0137a0001c0010t0033g0019 | 3 | HG00099.hp2 HG01256.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.317-9370T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038858 | ||||||
| chr3:125038919
|
G | A | 3 | a0001c0001t0070g0194a0004c0005t0010g0165a0041c0069t0111g0203 | 3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.317-9431C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038919 | ||||||
| chr3:125038920
|
C | T | 3 | a0001c0001t0070g0194a0004c0005t0010g0165a0041c0069t0111g0203 | 3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.317-9432G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038920 | ||||||
| chr3:125038933
|
T | C | 55 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(52): Show | 56 | HG00558.hp1 HG00735.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-9445A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038933 | ||||||
| chr3:125038948
|
G | A | 1 | a0001c0001t0008g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.317-9460C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038948 | ||||||
| chr3:125039011
|
C | A | 1 | a0020c0025t0025g0008 | 2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.317-9523G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039011 | ||||||
| chr3:125039044
|
T | C | 197 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.317-9556A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039044 | ||||||
| chr3:125039108
|
G | C | 1 | a0001c0001t0042g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.317-9620C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039108 | ||||||
| chr3:125039123
|
T | C | 1 | a0001c0002t0001g0132 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.317-9635A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039123 | ||||||
| chr3:125039467
|
C | T | 6 | a0001c0001t0059g0262a0005c0007t0055g0322a0021c0043t0063g0342others(3): Show | 6 | HG02148.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-9979G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039467 | ||||||
| chr3:125039475
|
C | T | 3 | a0002c0014t0006g0258a0002c0014t0075g0078a0002c0014t0121g0257 | 3 | NA19012.hp2 NA19067.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.317-9987G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039475 | ||||||
| chr3:125039835
|
C | CA | 14 | a0003c0004t0002g0089a0004c0048t0029g0023a0005c0007t0055g0322others(11): Show | 14 | HG00621.hp1 HG02155.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-10348dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | ||||||
| chr3:125039835
|
C | CAA | 176 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-10349_317-1034 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | ||||||
| chr3:125039835
|
C | CAAA | 12 | a0001c0001t0004g0279a0001c0001t0006g0283a0001c0001t0007g0113others(9): Show | 12 | HG01167.hp1 HG01346.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.317-10350_317-1034 others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | ||||||
| chr3:125039835
|
CA | C | 83 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(80): Show | 84 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.317-10348delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | ||||||
| chr3:125039842
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0016g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.317-10365_317-1035 others(15): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039842 | ||||||
| chr3:125039853
|
C | A | 47 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(44): Show | 48 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.317-10365G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039853 | ||||||
| chr3:125039863
|
C | G | 1 | a0001c0085t0132g0289 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.317-10375G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039863 | ||||||
| chr3:125040103
|
C | T | 2 | a0005c0007t0060g0334a0005c0007t0137g0337 | 2 | HG02155.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.317-10615G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040103 | ||||||
| chr3:125040107
|
G | T | 4 | a0006c0086t0090g0084a0018c0037t0063g0256a0020c0025t0025g0008others(1): Show | 5 | HG00735.hp2 HG01074.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-10619C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040107 | ||||||
| chr3:125040213
|
C | T | 339 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(336): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.317-10725G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040213 | ||||||
| chr3:125040294
|
T | C | 1 | a0004c0005t0028g0261 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.317-10806A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040294 | ||||||
| chr3:125040357
|
T | A | 44 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(41): Show | 44 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.317-10869A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040357 | ||||||
| chr3:125040476
|
G | A | 1 | a0001c0002t0072g0133 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.317-10988C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040476 | ||||||
| chr3:125040503
|
T | C | 48 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-11015A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040503 | ||||||
| chr3:125040521
|
G | A | 4 | a0006c0086t0090g0084a0018c0037t0063g0256a0020c0025t0025g0008others(1): Show | 5 | HG00735.hp2 HG01074.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-11033C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040521 | ||||||
| chr3:125040694
|
G | C | 1 | a0007c0011t0011g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.317-11206C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040694 | ||||||
| chr3:125040711
|
CT | C | 119 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(116): Show | 120 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.317-11224delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040711 | ||||||
| chr3:125040711
|
CTT | C | 24 | a0003c0004t0020g0062a0003c0004t0025g0273a0003c0067t0019g0063others(21): Show | 24 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.317-11225_317-1122 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040711 | ||||||
| chr3:125041002
|
C | T | 22 | a0003c0004t0020g0062a0003c0004t0025g0273a0003c0067t0019g0063others(19): Show | 22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.317-11514G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041002 | ||||||
| chr3:125041222
|
T | A | 19 | a0001c0001t0059g0262a0004c0005t0010g0044a0005c0007t0055g0322others(16): Show | 19 | HG01346.hp1 HG02148.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.317-11734A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041222 | ||||||
| chr3:125041242
|
G | A | 143 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(140): Show | 144 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.317-11754C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041242 | ||||||
| chr3:125041270
|
G | T | 42 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(39): Show | 42 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.317-11782C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041270 | ||||||
| chr3:125041271
|
G | A | 1 | a0001c0002t0001g0127 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.317-11783C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041271 | ||||||
| chr3:125041554
|
A | C | 20 | a0001c0001t0059g0262a0004c0005t0010g0044a0005c0007t0055g0322others(17): Show | 20 | HG01346.hp1 HG02148.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.317-12066T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041554 | ||||||
| chr3:125041604
|
G | C | 148 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(145): Show | 150 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.317-12116C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041604 | ||||||
| chr3:125041644
|
C | A | 1 | a0004c0005t0010g0202 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-12156G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041644 | ||||||
| chr3:125041724
|
A | C | 22 | a0003c0004t0020g0062a0003c0004t0025g0273a0003c0067t0019g0063others(19): Show | 22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.317-12236T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041724 | ||||||
| chr3:125041839
|
G | T | 95 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(92): Show | 96 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.317-12351C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041839 | ||||||
| chr3:125041908
|
G | T | 40 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.317-12420C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041908 | ||||||
| chr3:125042047
|
T | G | 5 | a0001c0001t0047g0122a0001c0001t0047g0123a0001c0001t0062g0280others(2): Show | 5 | NA18942.hp1 NA18977.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-12559A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042047 | ||||||
| chr3:125042376
|
C | T | 22 | a0003c0004t0020g0062a0003c0004t0025g0273a0003c0067t0019g0063others(19): Show | 22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.317-12888G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042376 | ||||||
| chr3:125042437
|
T | TA | 29 | a0001c0002t0016g0061a0001c0010t0001g0013a0001c0010t0001g0024others(26): Show | 29 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.317-12950dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042437 | ||||||
| chr3:125042503
|
G | A | 40 | a0001c0001t0011g0081a0001c0001t0011g0183a0001c0001t0092g0187others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.317-13015C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042503 | ||||||
| chr3:125042582
|
G | C | 9 | a0005c0007t0013g0307a0005c0007t0013g0314a0005c0007t0014g0309others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+12993C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042582 | ||||||
| chr3:125042743
|
T | C | 1 | a0001c0001t0011g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.316+12832A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042743 | ||||||
| chr3:125042751
|
A | C | 241 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(238): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.316+12824T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042751 | ||||||
| chr3:125042754
|
A | C | 1 | a0002c0003t0089g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.316+12821T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042754 | ||||||
| chr3:125042770
|
A | G | 160 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(157): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.316+12805T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042770 | ||||||
| chr3:125042882
|
C | T | 3 | a0001c0001t0070g0194a0004c0005t0010g0165a0041c0069t0111g0203 | 3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.316+12693G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042882 | ||||||
| chr3:125042883
|
G | A | 1 | a0057c0061t0035g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.316+12692C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042883 | ||||||
| chr3:125042918
|
C | T | 1 | a0002c0003t0007g0076 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.316+12657G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042918 | ||||||
| chr3:125043076
|
T | C | 296 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.316+12499A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043076 | ||||||
| chr3:125043077
|
G | A | 1 | a0001c0002t0016g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.316+12498C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043077 | ||||||
| chr3:125043123
|
G | A | 1 | a0001c0002t0001g0079 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.316+12452C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043123 | ||||||
| chr3:125043145
|
C | T | 1 | a0002c0003t0078g0073 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.316+12430G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043145 | ||||||
| chr3:125043391
|
A | G | 1 | a0007c0077t0073g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.316+12184T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043391 | ||||||
| chr3:125043420
|
G | GT | 52 | a0001c0001t0093g0162a0002c0003t0007g0069a0002c0003t0007g0070others(49): Show | 55 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.316+12154dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043420 | ||||||
| chr3:125043420
|
G | GTT | 16 | a0002c0003t0007g0076a0004c0005t0010g0044a0005c0007t0123g0351others(13): Show | 16 | HG01346.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.316+12153_316+1215 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043420 | ||||||
| chr3:125043474
|
T | C | 2 | a0003c0004t0039g0053a0003c0034t0030g0114 | 2 | HG03239.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.316+12101A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043474 | ||||||
| chr3:125043492
|
A | T | 2 | a0002c0003t0082g0184a0002c0071t0083g0185 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+12083T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043492 | ||||||
| chr3:125043524
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.316+12051C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043524 | ||||||
| chr3:125043957
|
G | A | 2 | a0020c0025t0025g0008a0020c0025t0130g0318 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.316+11618C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043957 | ||||||
| chr3:125043963
|
C | T | 1 | a0001c0001t0059g0262 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.316+11612G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043963 | ||||||
| chr3:125044080
|
C | T | 39 | a0001c0001t0093g0162a0002c0003t0007g0069a0002c0003t0007g0070others(36): Show | 42 | HG01975.hp2 HG02027.hp1 HG02074.hp2 others(39): Show |
intron_variant | MODIFIER | c.316+11495G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044080 | ||||||
| chr3:125044087
|
G | A | 1 | a0002c0003t0078g0073 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.316+11488C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044087 | ||||||
| chr3:125044183
|
G | C | 5 | a0001c0001t0011g0183a0001c0001t0092g0187a0009c0009t0011g0204others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+11392C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044183 | ||||||
| chr3:125044297
|
T | C | 1 | a0041c0069t0111g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+11278A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044297 | ||||||
| chr3:125044385
|
A | G | 112 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0007g0113others(109): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.316+11190T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044385 | ||||||
| chr3:125044472
|
C | T | 38 | a0001c0001t0093g0162a0002c0003t0007g0069a0002c0003t0007g0070others(35): Show | 41 | HG01975.hp2 HG02027.hp1 HG02074.hp2 others(38): Show |
intron_variant | MODIFIER | c.316+11103G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044472 | ||||||
| chr3:125045050
|
G | A | 1 | a0001c0002t0145g0353 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.316+10525C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045050 | ||||||
| chr3:125045084
|
A | C | 105 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0007g0113others(102): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.316+10491T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045084 | ||||||
| chr3:125045266
|
A | G | 99 | a0001c0001t0008g0244a0001c0001t0029g0153a0001c0001t0092g0187others(96): Show | 101 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.316+10309T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045266 | ||||||
| chr3:125045305
|
C | T | 1 | a0001c0001t0008g0247 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.316+10270G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045305 | ||||||
| chr3:125045306
|
G | A | 1 | a0003c0067t0019g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.316+10269C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045306 | ||||||
| chr3:125045377
|
T | C | 1 | a0006c0086t0090g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+10198A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045377 | ||||||
| chr3:125045463
|
C | T | 98 | a0001c0001t0008g0244a0001c0001t0029g0153a0001c0001t0092g0187others(95): Show | 100 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.316+10112G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045463 | ||||||
| chr3:125045535
|
G | A | 1 | a0030c0058t0057g0220 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.316+10040C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045535 | ||||||
| chr3:125045570
|
G | A | 130 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0007g0113others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.316+10005C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045570 | ||||||
| chr3:125045725
|
C | T | 1 | a0059c0057t0128g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316+9850G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045725 | ||||||
| chr3:125045740
|
C | T | 1 | a0045c0073t0056g0299 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.316+9835G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045740 | ||||||
| chr3:125045741
|
G | A | 1 | a0049c0051t0023g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.316+9834C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045741 | ||||||
| chr3:125045968
|
C | T | 1 | a0006c0086t0090g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+9607G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045968 | ||||||
| chr3:125046132
|
C | A | 1 | a0001c0001t0059g0262 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.316+9443G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046132 | ||||||
| chr3:125046317
|
C | T | 18 | a0001c0001t0008g0244a0003c0004t0020g0062a0003c0004t0025g0273others(15): Show | 18 | HG00741.hp1 HG01256.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.316+9258G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046317 | ||||||
| chr3:125046398
|
T | TAC | 10 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0113g0150others(7): Show | 10 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+9175_316+9176d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TAC | T | 25 | a0001c0001t0045g0128a0001c0002t0001g0129a0001c0002t0001g0130others(22): Show | 27 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+9175_316+9176d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TACAC | T | 11 | a0001c0001t0008g0244a0001c0001t0011g0081a0001c0001t0070g0194others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+9173_316+9176d others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TACACAC | T | 21 | a0001c0001t0059g0262a0001c0001t0093g0162a0002c0003t0003g0126others(18): Show | 21 | HG00673.hp2 HG00741.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.316+9171_316+9176d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TACACACA others(1): Show |
T | 42 | a0001c0001t0023g0059a0001c0001t0044g0103a0001c0001t0100g0095others(39): Show | 45 | HG00438.hp1 HG00544.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.316+9169_316+9176d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TACACACA others(3): Show |
T | 54 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(51): Show | 54 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.316+9167_316+9176d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TACACACA others(5): Show |
T | 27 | a0001c0001t0061g0290a0001c0001t0126g0274a0001c0001t0127g0301others(24): Show | 27 | HG00733.hp1 HG01071.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+9165_316+9176d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046398
|
TACACACA others(9): Show |
T | 1 | a0006c0086t0090g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+9161_316+9176d others(18): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | ||||||
| chr3:125046414
|
C | G | 25 | a0001c0001t0061g0290a0001c0001t0126g0274a0001c0001t0127g0301others(22): Show | 25 | HG00733.hp1 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.316+9161G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046414 | ||||||
| chr3:125046428
|
CACACACA others(1): Show |
C | 83 | a0001c0001t0029g0153a0001c0001t0092g0187a0001c0002t0016g0061others(80): Show | 85 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.316+9139_316+9146d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046428 | ||||||
| chr3:125046443
|
T | A | 3 | a0001c0001t0008g0244a0003c0004t0025g0273a0007c0015t0115g0055 | 3 | HG02293.hp1 NA18959.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.316+9132A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046443 | ||||||
| chr3:125046660
|
T | C | 1 | a0002c0003t0003g0173 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.316+8915A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046660 | ||||||
| chr3:125046763
|
A | G | 27 | a0001c0001t0061g0290a0001c0001t0126g0274a0001c0001t0127g0301others(24): Show | 27 | HG00733.hp1 HG01071.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+8812T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046763 | ||||||
| chr3:125046979
|
C | T | 3 | a0010c0016t0005g0222a0028c0036t0030g0067a0028c0036t0030g0119 | 3 | HG02083.hp2 HG02132.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.316+8596G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046979 | ||||||
| chr3:125047028
|
G | A | 1 | a0004c0005t0010g0044 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.316+8547C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047028 | ||||||
| chr3:125047402
|
T | C | 3 | a0007c0011t0022g0002a0007c0011t0086g0080a0036c0064t0067g0009 | 4 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+8173A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047402 | ||||||
| chr3:125047642
|
T | C | 163 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(160): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.316+7933A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047642 | ||||||
| chr3:125047735
|
A | G | 1 | a0038c0084t0019g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+7840T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047735 | ||||||
| chr3:125047882
|
C | CT | 5 | a0003c0004t0020g0062a0003c0067t0019g0063a0004c0005t0009g0077others(2): Show | 5 | HG01975.hp1 HG01981.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+7692dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047882 | ||||||
| chr3:125048015
|
T | C | 102 | a0001c0001t0007g0113a0001c0001t0012g0172a0001c0001t0029g0153others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.316+7560A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048015 | ||||||
| chr3:125048052
|
G | C | 1 | a0035c0065t0066g0012 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.316+7523C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048052 | ||||||
| chr3:125048216
|
A | C | 10 | a0001c0001t0012g0172a0002c0003t0003g0173a0003c0004t0002g0001others(7): Show | 12 | HG02027.hp1 NA18951.hp2 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.316+7359T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048216 | ||||||
| chr3:125048253
|
T | C | 92 | a0001c0001t0007g0113a0001c0001t0029g0153a0001c0001t0042g0097others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.316+7322A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048253 | ||||||
| chr3:125048306
|
T | C | 23 | a0001c0001t0010g0068a0001c0002t0001g0074a0001c0002t0001g0079others(20): Show | 23 | HG01346.hp1 HG02074.hp2 HG02132.hp2 others(20): Show |
intron_variant | MODIFIER | c.316+7269A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048306 | ||||||
| chr3:125048389
|
T | G | 36 | a0001c0001t0061g0290a0001c0002t0005g0292a0001c0002t0005g0298others(33): Show | 36 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.316+7186A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048389 | ||||||
| chr3:125048400
|
T | C | 1 | a0010c0022t0004g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.316+7175A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048400 | ||||||
| chr3:125048607
|
T | C | 2 | a0001c0001t0070g0194a0004c0005t0010g0165 | 2 | HG01109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316+6968A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048607 | ||||||
| chr3:125048691
|
TGTTAAGC others(3): Show |
T | 1 | a0015c0017t0096g0048 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.316+6874_316+6883d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048691 | ||||||
| chr3:125048801
|
G | T | 1 | a0013c0040t0059g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.316+6774C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048801 | ||||||
| chr3:125048830
|
A | G | 1 | a0012c0018t0055g0320 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.316+6745T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048830 | ||||||
| chr3:125048832
|
G | A | 37 | a0001c0001t0061g0290a0001c0002t0005g0292a0001c0002t0005g0298others(34): Show | 37 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.316+6743C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048832 | ||||||
| chr3:125048856
|
G | C | 2 | a0002c0014t0075g0078a0004c0005t0009g0077 | 2 | NA18955.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.316+6719C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048856 | ||||||
| chr3:125049066
|
A | G | 9 | a0001c0001t0011g0081a0007c0011t0022g0002a0007c0011t0086g0080others(6): Show | 10 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+6509T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049066 | ||||||
| chr3:125049092
|
G | A | 1 | a0001c0010t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.316+6483C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049092 | ||||||
| chr3:125049137
|
T | A | 3 | a0004c0005t0010g0066a0006c0006t0088g0065a0006c0086t0090g0084 | 3 | HG02280.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316+6438A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049137 | ||||||
| chr3:125049257
|
ACTTACAT others(4): Show |
A | 1 | a0002c0003t0015g0083 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.316+6307_316+6317d others(13): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049257 | ||||||
| chr3:125049264
|
T | C | 3 | a0005c0007t0123g0351a0012c0018t0056g0352a0055c0090t0119g0350 | 3 | HG00639.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.316+6311A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049264 | ||||||
| chr3:125049288
|
T | C | 1 | a0009c0009t0138g0348 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.316+6287A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049288 | ||||||
| chr3:125049376
|
G | A | 8 | a0001c0002t0016g0061a0003c0004t0020g0062a0003c0067t0019g0063others(5): Show | 8 | HG01981.hp1 HG02280.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+6199C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049376 | ||||||
| chr3:125049522
|
A | G | 97 | a0001c0001t0007g0113a0001c0001t0029g0153a0001c0001t0042g0097others(94): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.316+6053T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049522 | ||||||
| chr3:125049687
|
T | G | 1 | a0005c0007t0013g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.316+5888A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049687 | ||||||
| chr3:125049761
|
C | T | 9 | a0001c0001t0011g0081a0007c0011t0022g0002a0007c0011t0086g0080others(6): Show | 10 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+5814G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049761 | ||||||
| chr3:125049803
|
G | A | 1 | a0010c0022t0008g0233 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.316+5772C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049803 | ||||||
| chr3:125049827
|
G | A | 3 | a0005c0007t0123g0351a0012c0018t0056g0352a0055c0090t0119g0350 | 3 | HG00639.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.316+5748C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049827 | ||||||
| chr3:125050130
|
T | G | 1 | a0004c0005t0042g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.316+5445A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050130 | ||||||
| chr3:125050142
|
C | CT | 11 | a0001c0002t0016g0061a0005c0007t0013g0307a0005c0007t0013g0314others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+5432dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050142 | ||||||
| chr3:125050142
|
CT | C | 161 | a0001c0001t0004g0295a0001c0001t0004g0296a0001c0001t0007g0113others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.316+5432delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050142 | ||||||
| chr3:125050142
|
CTT | C | 28 | a0001c0002t0001g0079a0001c0002t0016g0051a0001c0002t0033g0050others(25): Show | 28 | HG00621.hp1 HG00639.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.316+5431_316+5432d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050142 | ||||||
| chr3:125050144
|
T | C | 2 | a0004c0005t0010g0202a0041c0069t0111g0203 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316+5431A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050144 | ||||||
| chr3:125050145
|
T | C | 4 | a0003c0004t0002g0089a0006c0006t0022g0088a0007c0077t0073g0087others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+5430A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050145 | ||||||
| chr3:125050166
|
T | A | 8 | a0001c0002t0016g0061a0003c0004t0020g0062a0003c0067t0019g0063others(5): Show | 8 | HG01981.hp1 HG02280.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+5409A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050166 | ||||||
| chr3:125050213
|
G | A | 20 | a0001c0010t0001g0013a0001c0010t0001g0022a0001c0010t0001g0024others(17): Show | 20 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+5362C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050213 | ||||||
| chr3:125050278
|
G | A | 1 | a0050c0050t0022g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+5297C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050278 | ||||||
| chr3:125050391
|
G | A | 9 | a0001c0001t0011g0081a0007c0011t0022g0002a0007c0011t0086g0080others(6): Show | 10 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+5184C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050391 | ||||||
| chr3:125050424
|
G | A | 1 | a0022c0026t0117g0306 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.316+5151C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050424 | ||||||
| chr3:125050442
|
C | A | 1 | a0001c0001t0044g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.316+5133G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050442 | ||||||
| chr3:125050554
|
C | G | 4 | a0005c0007t0123g0351a0012c0018t0056g0352a0013c0042t0004g0349others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+5021G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050554 | ||||||
| chr3:125050573
|
A | G | 1 | a0004c0081t0116g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.316+5002T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050573 | ||||||
| chr3:125050581
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.316+4994G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050581 | ||||||
| chr3:125050840
|
A | G | 24 | a0001c0002t0016g0051a0001c0002t0033g0050a0001c0010t0001g0013others(21): Show | 24 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(21): Show |
intron_variant | MODIFIER | c.316+4735T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050840 | ||||||
| chr3:125050868
|
T | C | 33 | a0001c0001t0011g0081a0001c0002t0016g0051a0001c0002t0033g0050others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+4707A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050868 | ||||||
| chr3:125050942
|
T | C | 5 | a0027c0032t0065g0011a0034c0066t0068g0010a0035c0065t0066g0012others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+4633A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050942 | ||||||
| chr3:125050952
|
C | T | 7 | a0011c0008t0004g0238a0011c0008t0027g0236a0011c0008t0027g0237others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+4623G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050952 | ||||||
| chr3:125051016
|
T | C | 2 | a0001c0002t0005g0298a0006c0006t0118g0297 | 2 | HG00733.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.316+4559A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051016 | ||||||
| chr3:125051221
|
T | A | 1 | a0006c0086t0090g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+4354A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051221 | ||||||
| chr3:125051238
|
A | G | 10 | a0016c0029t0007g0035a0016c0029t0020g0034a0024c0031t0012g0032others(7): Show | 10 | HG00323.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+4337T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051238 | ||||||
| chr3:125051346
|
CG | C | 33 | a0001c0001t0011g0081a0001c0002t0016g0051a0001c0002t0033g0050others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+4228delC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051346 | ||||||
| chr3:125051347
|
G | A | 6 | a0003c0004t0002g0089a0004c0005t0010g0202a0006c0006t0022g0088others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+4228C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051347 | ||||||
| chr3:125051391
|
A | AC | 6 | a0001c0001t0100g0095a0001c0002t0001g0091a0001c0002t0038g0245others(3): Show | 6 | HG00741.hp2 HG01243.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+4183dupG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051391 | ||||||
| chr3:125051456
|
C | G | 33 | a0001c0001t0011g0081a0001c0002t0016g0051a0001c0002t0033g0050others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+4119G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051456 | ||||||
| chr3:125051486
|
T | A | 1 | a0024c0031t0012g0032 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.316+4089A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051486 | ||||||
| chr3:125051493
|
G | C | 5 | a0027c0032t0065g0011a0034c0066t0068g0010a0035c0065t0066g0012others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+4082C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051493 | ||||||
| chr3:125051515
|
C | T | 1 | a0004c0005t0010g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.316+4060G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051515 | ||||||
| chr3:125051569
|
A | G | 192 | a0001c0001t0007g0113a0001c0001t0010g0068a0001c0001t0011g0081others(189): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.316+4006T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051569 | ||||||
| chr3:125051574
|
A | G | 1 | a0007c0015t0115g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.316+4001T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051574 | ||||||
| chr3:125051598
|
G | A | 1 | a0003c0068t0084g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.316+3977C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051598 | ||||||
| chr3:125051609
|
C | T | 3 | a0022c0026t0053g0304a0022c0026t0053g0305a0022c0026t0117g0306 | 3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.316+3966G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051609 | ||||||
| chr3:125051641
|
C | T | 1 | a0008c0013t0004g0212 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.316+3934G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051641 | ||||||
| chr3:125051693
|
T | C | 194 | a0001c0001t0007g0113a0001c0001t0010g0068a0001c0001t0011g0081others(191): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.316+3882A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051693 | ||||||
| chr3:125051833
|
G | C | 24 | a0001c0002t0016g0051a0001c0002t0033g0050a0001c0010t0001g0013others(21): Show | 24 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(21): Show |
intron_variant | MODIFIER | c.316+3742C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051833 | ||||||
| chr3:125052109
|
AC | A | 9 | a0016c0029t0007g0035a0016c0029t0020g0034a0024c0031t0043g0038others(6): Show | 9 | HG01361.hp1 HG01433.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+3465delG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052109 | ||||||
| chr3:125052126
|
G | A | 147 | a0001c0001t0007g0113a0001c0001t0010g0068a0001c0001t0011g0183others(144): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.316+3449C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052126 | ||||||
| chr3:125052131
|
C | T | 1 | a0001c0010t0001g0013 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316+3444G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052131 | ||||||
| chr3:125052132
|
T | G | 33 | a0001c0001t0011g0081a0001c0002t0016g0051a0001c0002t0033g0050others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+3443A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052132 | ||||||
| chr3:125052139
|
T | C | 1 | a0015c0017t0096g0048 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.316+3436A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052139 | ||||||
| chr3:125052237
|
C | A | 1 | a0004c0005t0011g0197 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.316+3338G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052237 | ||||||
| chr3:125052241
|
C | T | 19 | a0005c0007t0013g0307a0005c0007t0013g0314a0005c0007t0014g0309others(16): Show | 19 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.316+3334G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052241 | ||||||
| chr3:125052265
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.316+3310G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052265 | ||||||
| chr3:125052293
|
G | A | 2 | a0004c0005t0010g0202a0041c0069t0111g0203 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316+3282C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052293 | ||||||
| chr3:125052388
|
C | A | 220 | a0001c0001t0007g0113a0001c0001t0010g0068a0001c0001t0011g0081others(217): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.316+3187G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052388 | ||||||
| chr3:125052407
|
C | T | 4 | a0027c0032t0065g0011a0034c0066t0068g0010a0035c0065t0066g0012others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+3168G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052407 | ||||||
| chr3:125052454
|
G | A | 1 | a0001c0002t0005g0300 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.316+3121C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052454 | ||||||
| chr3:125052861
|
C | T | 86 | a0001c0001t0007g0113a0001c0001t0029g0153a0001c0001t0042g0097others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.316+2714G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052861 | ||||||
| chr3:125052936
|
G | T | 1 | a0005c0038t0131g0303 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.316+2639C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052936 | ||||||
| chr3:125053033
|
A | C | 33 | a0001c0001t0011g0081a0001c0002t0016g0051a0001c0002t0033g0050others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+2542T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053033 | ||||||
| chr3:125053060
|
C | T | 4 | a0001c0002t0001g0091a0001c0002t0024g0092a0001c0002t0024g0093others(1): Show | 4 | HG00140.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+2515G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053060 | ||||||
| chr3:125053238
|
C | T | 147 | a0001c0001t0007g0113a0001c0001t0010g0068a0001c0001t0011g0183others(144): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.316+2337G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053238 | ||||||
| chr3:125053300
|
A | G | 1 | a0038c0084t0019g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+2275T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053300 | ||||||
| chr3:125053520
|
T | C | 3 | a0011c0008t0036g0240a0011c0008t0036g0241a0011c0008t0036g0242 | 3 | HG00738.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.316+2055A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053520 | ||||||
| chr3:125053679
|
A | G | 26 | a0008c0012t0013g0227a0008c0012t0013g0228a0008c0012t0017g0006others(23): Show | 27 | HG00558.hp1 HG00558.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.316+1896T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053679 | ||||||
| chr3:125053724
|
T | C | 1 | a0032c0055t0002g0040 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.316+1851A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053724 | ||||||
| chr3:125053747
|
C | T | 9 | a0006c0086t0090g0084a0016c0029t0007g0035a0016c0029t0020g0034others(6): Show | 9 | HG01361.hp1 HG01433.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+1828G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053747 | ||||||
| chr3:125053871
|
C | T | 19 | a0001c0001t0010g0068a0001c0001t0011g0081a0001c0002t0001g0074others(16): Show | 20 | HG01884.hp2 HG02074.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+1704G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053871 | ||||||
| chr3:125053927
|
C | G | 1 | a0039c0087t0021g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.316+1648G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053927 | ||||||
| chr3:125054069
|
G | A | 54 | a0001c0001t0010g0068a0001c0001t0011g0081a0001c0002t0001g0074others(51): Show | 55 | HG00621.hp1 HG00639.hp2 HG01361.hp1 others(52): Show |
intron_variant | MODIFIER | c.316+1506C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054069 | ||||||
| chr3:125054139
|
T | C | 5 | a0003c0004t0002g0089a0006c0006t0022g0088a0007c0077t0073g0087others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+1436A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054139 | ||||||
| chr3:125054326
|
CA | C | 20 | a0001c0010t0001g0013a0001c0010t0001g0022a0001c0010t0001g0024others(17): Show | 20 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+1248delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054326 | ||||||
| chr3:125054669
|
C | T | 1 | a0002c0003t0003g0003 | 2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.316+906G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054669 | ||||||
| chr3:125054831
|
G | A | 127 | a0001c0001t0007g0113a0001c0001t0011g0183a0001c0001t0012g0172others(124): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.316+744C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054831 | ||||||
| chr3:125054910
|
G | A | 1 | a0027c0032t0026g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.316+665C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054910 | ||||||
| chr3:125055052
|
C | A | 1 | a0008c0013t0124g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.316+523G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055052 | ||||||
| chr3:125055415
|
T | A | 4 | a0005c0007t0123g0351a0012c0018t0056g0352a0013c0042t0004g0349others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+160A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055415 | ||||||
| chr3:125055446
|
A | T | 1 | a0001c0001t0077g0043 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.316+129T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055446 | ||||||
| chr3:125055476
|
G | T | 1 | a0006c0006t0009g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.316+99C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055476 | ||||||
| chr3:125055516
|
G | A | 2 | a0004c0005t0010g0202a0041c0069t0111g0203 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316+59C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055516 | ||||||
| chr3:125055564
|
C | T | 1 | a0059c0057t0128g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316+11G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055564 |