| geneid | 50939 |
|---|---|
| ensemblid | ENSG00000081148.12 |
| hgncid | 18362 |
| symbol | IMPG2 |
| name | interphotoreceptor matrix proteoglycan 2 |
| refseq_nuc | NM_016247.4 |
| refseq_prot | NP_057331.2 |
| ensembl_nuc | ENST00000193391.8 |
| ensembl_prot | ENSP00000193391.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 101222546 |
| end | 101320575 |
| strand | - |
| ver | v1.2 |
| region | chr3:101222546-101320575 |
| region5000 | chr3:101217546-101325575 |
| regionname0 | IMPG2_chr3_101222546_101320575 |
| regionname5000 | IMPG2_chr3_101217546_101325575 |
| 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 | 0/0 | 1241 | 215 | 53 | 37 | 95 | 8 | 22 | 77 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002 | 1/1 | 1241 | 125 | 28 | 25 | 49 | 8 | 13 | 38 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003 | 0/0 | 1241 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0004 | 0/0 | 1241 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0005 | 0/0 | 1241 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0006 | 0/0 | 1241 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0007 | 0/0 | 9 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0008 | 0/0 | 1241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0009 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0010 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0011 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0012 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0013 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0014 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| 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 | 3726 | 214 | 53 | 37 | 94 | 8 | 22 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0002 | 1/1 | 3726 | 62 | 14 | 12 | 20 | 6 | 8 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0003 | 0/0 | 3726 | 62 | 14 | 13 | 28 | 2 | 5 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0004 | 0/0 | 3726 | 4 | 4 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0005 | 0/0 | 3726 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0006 | 0/0 | 3726 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0007 | 0/0 | 3726 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0008 | 0/0 | 3710 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0009 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0010 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0011 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0012 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0013 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0014 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0015 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0016 | 0/0 | 3726 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0017 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0018 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| c0019 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| 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 | 4573 | 94 | 21 | 16 | 43 | 4 | 9 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0002 | 0/0 | 4593 | 22 | 2 | 5 | 13 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0003 | 0/0 | 4595 | 16 | 1 | 2 | 9 | 1 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0004 | 0/0 | 4623 | 10 | 1 | 0 | 8 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0005 | 0/0 | 4597 | 9 | 1 | 2 | 5 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0006 | 0/0 | 4605 | 9 | 1 | 3 | 3 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0007 | 0/0 | 4615 | 9 | 2 | 0 | 7 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0008 | 0/0 | 4583 | 8 | 0 | 7 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0009 | 0/0 | 4619 | 8 | 1 | 0 | 4 | 0 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0010 | 0/0 | 4619 | 7 | 1 | 1 | 3 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0011 | 0/0 | 4617 | 7 | 0 | 3 | 1 | 2 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0012 | 0/0 | 4617 | 6 | 1 | 0 | 5 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0013 | 0/0 | 4621 | 6 | 0 | 0 | 4 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0014 | 0/0 | 4627 | 6 | 0 | 1 | 3 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0015 | 0/0 | 4625 | 6 | 1 | 1 | 3 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0016 | 0/0 | 4625 | 5 | 0 | 0 | 5 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0017 | 1/0 | 4627 | 5 | 0 | 0 | 2 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0018 | 0/0 | 4579 | 5 | 4 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0019 | 0/0 | 4591 | 4 | 2 | 1 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0020 | 0/0 | 4611 | 4 | 0 | 2 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0021 | 0/0 | 4623 | 4 | 1 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0022 | 0/0 | 4629 | 4 | 0 | 1 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0023 | 0/0 | 4575 | 3 | 0 | 0 | 1 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0024 | 0/0 | 4599 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0025 | 0/0 | 4607 | 3 | 1 | 0 | 1 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0026 | 0/0 | 4621 | 3 | 0 | 1 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0027 | 0/0 | 4635 | 3 | 0 | 1 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0028 | 0/0 | 4583 | 2 | 0 | 0 | 0 | 2 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0029 | 0/0 | 4573 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0030 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0031 | 0/0 | 4601 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0032 | 0/0 | 4603 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0033 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0034 | 0/0 | 4609 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0035 | 0/0 | 4617 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0036 | 0/0 | 4621 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0037 | 0/0 | 4631 | 2 | 0 | 1 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0038 | 0/0 | 4617 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0039 | 0/0 | 4615 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0040 | 0/0 | 4631 | 2 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0041 | 0/0 | 4633 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0042 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0043 | 0/0 | 4573 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0044 | 0/0 | 4589 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0045 | 0/0 | 4575 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0046 | 0/0 | 4577 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0047 | 0/0 | 4589 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0048 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0049 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0050 | 0/0 | 4571 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0051 | 0/0 | 4571 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0052 | 0/0 | 4573 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0053 | 0/0 | 4573 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0054 | 0/0 | 4589 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0055 | 0/0 | 4573 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0056 | 0/0 | 4591 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0057 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0058 | 0/0 | 4643 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0059 | 0/0 | 4595 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0060 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0061 | 0/0 | 4683 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0062 | 0/0 | 4601 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0063 | 0/0 | 4601 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0064 | 0/0 | 4603 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0065 | 0/0 | 4603 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0066 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0067 | 0/0 | 4607 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0068 | 0/0 | 4607 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0069 | 0/0 | 4607 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0070 | 0/0 | 4611 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0071 | 0/0 | 4611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0072 | 0/0 | 4611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0073 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0074 | 0/0 | 4617 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0075 | 0/0 | 4619 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0076 | 0/0 | 4619 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0077 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0078 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0079 | 0/0 | 4623 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0080 | 0/0 | 4623 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0081 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0082 | 0/0 | 4585 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0083 | 0/0 | 4623 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0084 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0085 | 0/0 | 4611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0086 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0087 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0088 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0089 | 0/0 | 4643 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0090 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0091 | 0/0 | 4625 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0092 | 0/0 | 4585 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0093 | 0/0 | 4619 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0094 | 0/0 | 4629 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0095 | 0/0 | 4627 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0096 | 0/0 | 4637 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0097 | 0/0 | 4643 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0098 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0099 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0100 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0101 | 0/0 | 4616 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0102 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0103 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| t0104 | 0/0 | 4573 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| 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 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| 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 | 3726 | 214 | 53 | 37 | 94 | 8 | 22 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0017 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002 | 1/1 | 3726 | 62 | 14 | 12 | 20 | 6 | 8 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003 | 0/0 | 3726 | 62 | 14 | 13 | 28 | 2 | 5 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0013 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0004 | 0/0 | 3726 | 4 | 4 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0009 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0014 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0004c0007 | 0/0 | 3726 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0005c0006 | 0/0 | 3726 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0006c0005 | 0/0 | 3726 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0007c0008 | 0/0 | 3710 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0008c0015 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0009c0016 | 0/0 | 3726 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0010c0011 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0011c0012 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0012c0010 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0013c0018 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0014c0019 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8298 | 89 | 21 | 14 | 42 | 4 | 8 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0006 | 0/0 | 8330 | 9 | 1 | 3 | 3 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0007 | 0/0 | 8340 | 9 | 2 | 0 | 7 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0008 | 0/0 | 8308 | 8 | 0 | 7 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0010 | 0/0 | 8344 | 7 | 1 | 1 | 3 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0012 | 0/0 | 8342 | 6 | 1 | 0 | 5 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0013 | 0/0 | 8346 | 6 | 0 | 0 | 4 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0014 | 0/0 | 8352 | 6 | 0 | 1 | 3 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0016 | 0/0 | 8350 | 5 | 0 | 0 | 5 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0020 | 0/0 | 8336 | 4 | 0 | 2 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0021 | 0/0 | 8348 | 3 | 1 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0022 | 0/0 | 8354 | 4 | 0 | 1 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0023 | 0/0 | 8300 | 3 | 0 | 0 | 1 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0025 | 0/0 | 8332 | 3 | 1 | 0 | 1 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0028 | 0/0 | 8308 | 2 | 0 | 0 | 0 | 2 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0029 | 0/0 | 8298 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0030 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0032 | 0/0 | 8328 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0033 | 0/0 | 8334 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0034 | 0/0 | 8334 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0035 | 0/0 | 8342 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0036 | 0/0 | 8346 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0037 | 0/0 | 8356 | 2 | 0 | 1 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0043 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0050 | 0/0 | 8296 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0051 | 0/0 | 8296 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0052 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0053 | 0/0 | 8298 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0054 | 0/0 | 8314 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0055 | 0/0 | 8298 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0058 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0059 | 0/0 | 8320 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0060 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0061 | 0/0 | 8408 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0062 | 0/0 | 8326 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0063 | 0/0 | 8326 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0064 | 0/0 | 8328 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0065 | 0/0 | 8328 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0066 | 0/0 | 8330 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0068 | 0/0 | 8332 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0069 | 0/0 | 8332 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0070 | 0/0 | 8336 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0071 | 0/0 | 8336 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0072 | 0/0 | 8336 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0073 | 0/0 | 8338 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0074 | 0/0 | 8342 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0077 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0078 | 0/0 | 8346 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0079 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0080 | 0/0 | 8348 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0081 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0082 | 0/0 | 8310 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0099 | 0/0 | 8337 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0100 | 0/0 | 8339 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0101 | 0/0 | 8341 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0102 | 0/0 | 8347 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0001t0104 | 0/0 | 8298 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0001c0017t0001 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0001 | 0/1 | 8298 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0004 | 0/0 | 8348 | 7 | 1 | 0 | 5 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0009 | 0/0 | 8344 | 6 | 1 | 0 | 2 | 0 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0011 | 0/0 | 8342 | 7 | 0 | 3 | 1 | 2 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0015 | 0/0 | 8350 | 6 | 1 | 1 | 3 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0017 | 1/0 | 8352 | 4 | 0 | 0 | 1 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0026 | 0/0 | 8346 | 3 | 0 | 1 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0027 | 0/0 | 8360 | 3 | 0 | 1 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0038 | 0/0 | 8342 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0039 | 0/0 | 8340 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0040 | 0/0 | 8356 | 2 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0041 | 0/0 | 8358 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0042 | 0/0 | 8346 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0083 | 0/0 | 8348 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0084 | 0/0 | 8320 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0085 | 0/0 | 8336 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0086 | 0/0 | 8338 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0087 | 0/0 | 8352 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0088 | 0/0 | 8360 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0089 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0090 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0091 | 0/0 | 8350 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0092 | 0/0 | 8310 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0093 | 0/0 | 8344 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0094 | 0/0 | 8354 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0095 | 0/0 | 8352 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0096 | 0/0 | 8362 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0097 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0002t0103 | 0/0 | 8345 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0002 | 0/0 | 8318 | 21 | 2 | 5 | 12 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0003 | 0/0 | 8320 | 16 | 1 | 2 | 9 | 1 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0005 | 0/0 | 8322 | 8 | 1 | 2 | 4 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0018 | 0/0 | 8304 | 5 | 4 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0019 | 0/0 | 8316 | 3 | 2 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0024 | 0/0 | 8324 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0031 | 0/0 | 8326 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0056 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0057 | 0/0 | 8318 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0067 | 0/0 | 8332 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0075 | 0/0 | 8344 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0003t0098 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0002c0013t0019 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0004t0045 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0004t0046 | 0/0 | 8302 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0004t0047 | 0/0 | 8314 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0004t0048 | 0/0 | 8334 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0009t0049 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0003c0014t0044 | 0/0 | 8314 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0004c0007t0001 | 0/0 | 8298 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0005c0006t0004 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0005c0006t0009 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0006c0005t0004 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0006c0005t0009 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0007c0008t0024 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0008c0015t0076 | 0/0 | 8344 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0009c0016t0001 | 0/0 | 8298 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0010c0011t0004 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0011c0012t0002 | 0/0 | 8318 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0012c0010t0017 | 0/0 | 8352 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0013c0018t0005 | 0/0 | 8322 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| a0014c0019t0021 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | copy fasta | chr3 | 101217546 | 101325575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0021g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0021g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0021g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0023g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0023g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0023g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0025g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0025g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0025g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0028g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0028g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0029g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0029g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0030g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0030g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0032g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0032g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0033g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0033g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0034g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0034g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0035g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0035g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0036g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0036g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0037g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0037g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0043g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0050g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0051g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0052g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0053g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0054g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0055g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0058g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0059g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0060g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0061g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0062g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0063g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0064g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0065g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0066g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0068g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0069g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0070g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0071g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0072g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0073g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0074g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0077g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0078g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0079g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0080g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0081g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0082g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0099g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0100g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0101g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0102g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0104g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0017t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0001g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0026g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0026g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0026g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0027g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0027g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0027g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0038g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0038g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0039g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0039g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0040g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0040g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0041g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0041g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0042g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0083g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0084g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0085g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0086g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0087g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0088g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0089g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0090g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0091g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0092g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0093g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0094g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0095g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0096g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0097g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0103g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0019g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0019g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0019g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0024g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0024g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0031g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0031g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0056g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0057g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0067g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0075g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0098g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0013t0019g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0045g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0046g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0047g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0048g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0009t0049g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0014t0044g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0004c0007t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0004c0007t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0005c0006t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0005c0006t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0006c0005t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0006c0005t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0007c0008t0024g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0008c0015t0076g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0009c0016t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0010c0011t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0011c0012t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0012c0010t0017g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0013c0018t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0014c0019t0021g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00099 | hp2 | a0002 | c0002 | t0096 | g0210 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00140 | hp1 | a0002 | c0003 | t0003 | g0272 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00140 | hp2 | a0002 | c0002 | t0015 | g0324 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0032 | EUR | FIN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00280 | hp2 | a0002 | c0002 | t0011 | g0322 | EUR | FIN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0274 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00423 | hp1 | a0002 | c0003 | t0024 | g0305 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00423 | hp2 | a0010 | c0011 | t0004 | g0200 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00438 | hp1 | a0002 | c0002 | t0004 | g0236 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0071 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00597 | hp2 | a0002 | c0003 | t0002 | g0278 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00621 | hp1 | a0001 | c0001 | t0022 | g0059 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00621 | hp2 | a0002 | c0002 | t0009 | g0214 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00639 | hp2 | a0002 | c0003 | t0075 | g0268 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00642 | hp2 | a0002 | c0002 | t0011 | g0004 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00673 | hp1 | a0002 | c0003 | t0002 | g0265 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0291 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00733 | hp2 | a0001 | c0001 | t0055 | g0124 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00735 | hp1 | a0002 | c0003 | t0002 | g0290 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00735 | hp2 | a0001 | c0001 | t0054 | g0145 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00741 | hp1 | a0002 | c0003 | t0067 | g0284 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0104 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0098 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01070 | hp2 | a0001 | c0001 | t0029 | g0188 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01071 | hp1 | a0002 | c0002 | t0011 | g0004 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01071 | hp2 | a0001 | c0001 | t0029 | g0191 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0097 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01081 | hp2 | a0002 | c0003 | t0002 | g0303 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01099 | hp1 | a0002 | c0002 | t0026 | g0323 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01106 | hp1 | a0002 | c0003 | t0019 | g0308 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01106 | hp2 | a0002 | c0002 | t0039 | g0327 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01167 | hp2 | a0002 | c0003 | t0005 | g0295 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01169 | hp1 | a0002 | c0003 | t0005 | g0293 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01169 | hp2 | a0002 | c0002 | t0027 | g0211 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01175 | hp2 | a0002 | c0002 | t0011 | g0328 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01255 | hp1 | a0004 | c0007 | t0001 | g0173 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01255 | hp2 | a0002 | c0002 | t0039 | g0326 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01256 | hp2 | a0001 | c0001 | t0032 | g0099 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01258 | hp2 | a0001 | c0001 | t0032 | g0081 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01261 | hp2 | a0001 | c0001 | t0037 | g0068 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01358 | hp1 | a0004 | c0007 | t0001 | g0177 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0048 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0306 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0035 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01515 | hp2 | a0001 | c0001 | t0028 | g0052 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01516 | hp1 | a0002 | c0002 | t0017 | g0198 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01516 | hp2 | a0002 | c0002 | t0095 | g0325 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01517 | hp1 | a0002 | c0002 | t0011 | g0004 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01517 | hp2 | a0001 | c0001 | t0028 | g0051 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01884 | hp1 | a0001 | c0001 | t0069 | g0229 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01891 | hp1 | a0003 | c0009 | t0049 | g0255 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01891 | hp2 | a0001 | c0001 | t0021 | g0031 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01943 | hp1 | a0002 | c0002 | t0083 | g0320 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01943 | hp2 | a0001 | c0001 | t0022 | g0077 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01952 | hp1 | a0002 | c0002 | t0094 | g0225 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01952 | hp2 | a0001 | c0001 | t0070 | g0109 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01975 | hp1 | a0002 | c0003 | t0018 | g0223 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01981 | hp1 | a0002 | c0003 | t0002 | g0302 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01981 | hp2 | a0002 | c0002 | t0092 | g0184 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0304 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02004 | hp1 | a0002 | c0002 | t0015 | g0204 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02004 | hp2 | a0001 | c0001 | t0020 | g0066 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02015 | hp2 | a0002 | c0003 | t0024 | g0264 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0062 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0047 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02055 | hp1 | a0001 | c0001 | t0078 | g0111 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02055 | hp2 | a0001 | c0001 | t0036 | g0252 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02071 | hp1 | a0001 | c0017 | t0001 | g0155 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02071 | hp2 | a0001 | c0001 | t0012 | g0076 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02074 | hp2 | a0001 | c0001 | t0012 | g0085 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02080 | hp1 | a0002 | c0002 | t0097 | g0205 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02080 | hp2 | a0001 | c0001 | t0013 | g0070 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02129 | hp2 | a0002 | c0002 | t0011 | g0185 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02145 | hp1 | a0001 | c0001 | t0030 | g0335 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02145 | hp2 | a0002 | c0003 | t0005 | g0282 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02148 | hp2 | a0002 | c0002 | t0040 | g0209 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02155 | hp1 | a0001 | c0001 | t0013 | g0030 | EAS | CDX | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02258 | hp1 | a0002 | c0003 | t0003 | g0289 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0089 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02273 | hp2 | a0001 | c0001 | t0008 | g0033 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02280 | hp1 | a0001 | c0001 | t0068 | g0311 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0034 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02451 | hp1 | a0003 | c0004 | t0048 | g0345 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02451 | hp2 | a0002 | c0002 | t0086 | g0094 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02572 | hp2 | a0001 | c0001 | t0035 | g0026 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02602 | hp1 | a0001 | c0001 | t0025 | g0088 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02602 | hp2 | a0002 | c0002 | t0093 | g0224 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02615 | hp1 | a0001 | c0001 | t0058 | g0334 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02615 | hp2 | a0002 | c0002 | t0090 | g0339 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0314 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02630 | hp1 | a0001 | c0001 | t0081 | g0333 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02630 | hp2 | a0003 | c0004 | t0046 | g0330 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0256 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02698 | hp1 | a0002 | c0003 | t0002 | g0261 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02717 | hp1 | a0001 | c0001 | t0060 | g0337 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02717 | hp2 | a0001 | c0001 | t0073 | g0108 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02735 | hp1 | a0002 | c0003 | t0003 | g0259 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0087 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02809 | hp2 | a0002 | c0003 | t0018 | g0222 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02818 | hp2 | a0001 | c0001 | t0061 | g0332 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02886 | hp1 | a0001 | c0001 | t0066 | g0231 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02886 | hp2 | a0002 | c0002 | t0015 | g0318 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02895 | hp1 | a0001 | c0001 | t0072 | g0230 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02922 | hp1 | a0002 | c0003 | t0018 | g0220 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02922 | hp2 | a0002 | c0003 | t0019 | g0307 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02965 | hp2 | a0001 | c0001 | t0036 | g0249 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0110 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02976 | hp2 | a0002 | c0002 | t0038 | g0226 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03017 | hp1 | a0001 | c0001 | t0013 | g0065 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03017 | hp2 | a0001 | c0001 | t0064 | g0064 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03041 | hp1 | a0008 | c0015 | t0076 | g0027 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03098 | hp1 | a0001 | c0001 | t0030 | g0336 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0317 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0025 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03130 | hp2 | a0002 | c0003 | t0031 | g0301 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03139 | hp1 | a0001 | c0001 | t0080 | g0248 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03195 | hp1 | a0001 | c0001 | t0033 | g0313 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03195 | hp2 | a0002 | c0003 | t0018 | g0219 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03209 | hp2 | a0002 | c0002 | t0103 | g0315 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03225 | hp1 | a0002 | c0002 | t0084 | g0086 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03239 | hp2 | a0002 | c0003 | t0003 | g0309 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03453 | hp1 | a0002 | c0002 | t0042 | g0012 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03453 | hp2 | a0002 | c0003 | t0098 | g0243 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03486 | hp1 | a0002 | c0002 | t0085 | g0341 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03486 | hp2 | a0001 | c0001 | t0071 | g0251 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0005 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03490 | hp2 | a0001 | c0001 | t0023 | g0163 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03491 | hp1 | a0002 | c0002 | t0009 | g0029 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03491 | hp2 | a0009 | c0016 | t0001 | g0167 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03492 | hp1 | a0002 | c0002 | t0009 | g0199 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03492 | hp2 | a0001 | c0001 | t0014 | g0005 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03540 | hp1 | a0002 | c0003 | t0002 | g0294 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03540 | hp2 | a0002 | c0003 | t0018 | g0221 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03579 | hp1 | a0001 | c0001 | t0074 | g0250 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03579 | hp2 | a0003 | c0004 | t0045 | g0344 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03654 | hp2 | a0002 | c0003 | t0005 | g0310 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03669 | hp1 | a0002 | c0002 | t0009 | g0319 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0091 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03688 | hp1 | a0001 | c0001 | t0082 | g0096 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03688 | hp2 | a0002 | c0002 | t0017 | g0234 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03710 | hp2 | a0002 | c0002 | t0011 | g0329 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04115 | hp1 | a0001 | c0001 | t0053 | g0160 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04115 | hp2 | a0002 | c0002 | t0040 | g0195 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04204 | hp1 | a0001 | c0001 | t0104 | g0159 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0079 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04228 | hp1 | a0001 | c0001 | t0023 | g0169 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0260 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18522 | hp1 | a0001 | c0001 | t0033 | g0312 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18747 | hp1 | a0002 | c0002 | t0015 | g0102 | EAS | CHB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18906 | hp1 | a0002 | c0002 | t0087 | g0340 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18941 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18942 | hp1 | a0001 | c0001 | t0100 | g0171 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18945 | hp1 | a0006 | c0005 | t0009 | g0216 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0285 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0196 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18948 | hp1 | a0001 | c0001 | t0062 | g0057 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18948 | hp2 | a0002 | c0002 | t0017 | g0213 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18950 | hp1 | a0001 | c0001 | t0016 | g0075 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18953 | hp2 | a0002 | c0003 | t0003 | g0266 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18954 | hp1 | a0001 | c0001 | t0012 | g0074 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18957 | hp1 | a0007 | c0008 | t0024 | g0013 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18957 | hp2 | a0001 | c0001 | t0020 | g0021 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18959 | hp1 | a0001 | c0001 | t0059 | g0039 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18959 | hp2 | a0001 | c0001 | t0052 | g0175 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18963 | hp1 | a0002 | c0003 | t0002 | g0286 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18965 | hp2 | a0001 | c0001 | t0016 | g0092 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0053 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18966 | hp2 | a0005 | c0006 | t0004 | g0201 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18969 | hp1 | a0002 | c0003 | t0002 | g0297 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18969 | hp2 | a0005 | c0006 | t0009 | g0206 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18970 | hp1 | a0002 | c0013 | t0019 | g0277 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18970 | hp2 | a0001 | c0001 | t0016 | g0157 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18971 | hp2 | a0002 | c0003 | t0005 | g0275 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18973 | hp1 | a0002 | c0003 | t0003 | g0288 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18973 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18974 | hp1 | a0001 | c0001 | t0034 | g0020 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18975 | hp2 | a0002 | c0002 | t0026 | g0235 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18977 | hp1 | a0002 | c0002 | t0041 | g0046 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18978 | hp2 | a0001 | c0001 | t0037 | g0073 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18979 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18983 | hp1 | a0001 | c0001 | t0016 | g0061 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18983 | hp2 | a0002 | c0003 | t0005 | g0276 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18986 | hp1 | a0002 | c0002 | t0015 | g0186 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18986 | hp2 | a0001 | c0001 | t0014 | g0042 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18990 | hp1 | a0002 | c0003 | t0003 | g0298 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18990 | hp2 | a0012 | c0010 | t0017 | g0218 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18991 | hp2 | a0002 | c0003 | t0002 | g0299 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18993 | hp2 | a0001 | c0001 | t0021 | g0049 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18994 | hp1 | a0001 | c0001 | t0022 | g0056 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18994 | hp2 | a0002 | c0003 | t0003 | g0281 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18995 | hp2 | a0001 | c0001 | t0079 | g0036 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18997 | hp1 | a0001 | c0001 | t0013 | g0024 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18997 | hp2 | a0013 | c0018 | t0005 | g0269 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18998 | hp2 | a0011 | c0012 | t0002 | g0287 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18999 | hp1 | a0001 | c0001 | t0014 | g0023 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19001 | hp1 | a0002 | c0003 | t0003 | g0263 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19001 | hp2 | a0002 | c0002 | t0041 | g0083 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19002 | hp1 | a0002 | c0002 | t0004 | g0203 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19002 | hp2 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19003 | hp2 | a0002 | c0003 | t0002 | g0283 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0207 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19010 | hp1 | a0002 | c0003 | t0005 | g0279 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19010 | hp2 | a0001 | c0001 | t0012 | g0067 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19012 | hp1 | a0002 | c0002 | t0027 | g0084 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19030 | hp1 | a0003 | c0014 | t0044 | g0232 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19030 | hp2 | a0002 | c0002 | t0038 | g0342 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19043 | hp2 | a0002 | c0003 | t0019 | g0270 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19056 | hp1 | a0001 | c0001 | t0020 | g0060 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19056 | hp2 | a0006 | c0005 | t0004 | g0215 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19057 | hp1 | a0002 | c0003 | t0003 | g0280 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19057 | hp2 | a0001 | c0001 | t0101 | g0127 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19058 | hp1 | a0002 | c0003 | t0003 | g0273 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19058 | hp2 | a0001 | c0001 | t0025 | g0058 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19060 | hp2 | a0001 | c0001 | t0021 | g0045 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19062 | hp1 | a0001 | c0001 | t0077 | g0043 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19062 | hp2 | a0002 | c0002 | t0015 | g0194 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19063 | hp1 | a0001 | c0001 | t0034 | g0040 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19065 | hp1 | a0001 | c0001 | t0023 | g0152 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0041 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0103 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19068 | hp2 | a0002 | c0002 | t0026 | g0197 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19070 | hp1 | a0014 | c0019 | t0021 | g0063 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19070 | hp2 | a0002 | c0002 | t0027 | g0228 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19074 | hp2 | a0001 | c0001 | t0102 | g0126 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19075 | hp2 | a0001 | c0001 | t0063 | g0080 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19085 | hp2 | a0002 | c0003 | t0002 | g0271 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19086 | hp1 | a0002 | c0002 | t0009 | g0217 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19086 | hp2 | a0001 | c0001 | t0022 | g0095 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19089 | hp1 | a0001 | c0001 | t0099 | g0082 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19089 | hp2 | a0002 | c0003 | t0002 | g0267 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19090 | hp2 | a0002 | c0003 | t0005 | g0296 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19091 | hp2 | a0002 | c0002 | t0091 | g0202 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19240 | hp1 | a0001 | c0001 | t0065 | g0233 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19240 | hp2 | a0002 | c0003 | t0056 | g0253 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0019 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20805 | hp1 | a0002 | c0003 | t0002 | g0292 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0078 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01123 | hp2 | a0002 | c0003 | t0003 | g0257 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02109 | hp2 | a0001 | c0001 | t0025 | g0106 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02486 | hp1 | a0001 | c0001 | t0051 | g0244 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02486 | hp2 | a0002 | c0002 | t0009 | g0316 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02559 | hp1 | a0003 | c0004 | t0047 | g0343 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03471 | hp1 | a0002 | c0002 | t0089 | g0338 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03471 | hp2 | a0002 | c0003 | t0031 | g0300 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18955 | hp1 | a0002 | c0003 | t0057 | g0258 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20300 | hp1 | a0001 | c0001 | t0050 | g0245 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20300 | hp2 | a0001 | c0001 | t0043 | g0148 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA21309 | hp2 | a0002 | c0002 | t0088 | g0331 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0044 | REF | REF | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0017 | g0321 | REF | REF | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101229574
|
G | A | 1 | a0003 | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.3439C>T | p.Pro1147Ser | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/19 | 3642/8352 | 3439/3726 | 1147/1241 | chr3 | 101229574 | ||
| chr3:101231081
|
C | T | 1 | a0011 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.3298G>A | p.Val1100Met | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/19 | 3501/8352 | 3298/3726 | 1100/1241 | chr3 | 101231081 | ||
| chr3:101232976
|
G | A | 1 | a0009 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.3038C>T | p.Pro1013Leu | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/19 | 3241/8352 | 3038/3726 | 1013/1241 | chr3 | 101232976 | ||
| chr3:101243693
|
C | T | 1 | a0010 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.2638G>A | p.Val880Met | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2841/8352 | 2638/3726 | 880/1241 | chr3 | 101243693 | ||
| chr3:101243717
|
C | T | 1 | a0008 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2614G>A | p.Val872Ile | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2817/8352 | 2614/3726 | 872/1241 | chr3 | 101243717 | ||
| chr3:101243900
|
A | C | 1 | a0006 | 2 | NA18945.hp1 NA19056.hp2 |
missense_variant | MODERATE | c.2431T>G | p.Ser811Ala | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2634/8352 | 2431/3726 | 811/1241 | chr3 | 101243900 | ||
| chr3:101244260
|
C | T | 1 | a0012 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.2071G>A | p.Ala691Thr | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2274/8352 | 2071/3726 | 691/1241 | chr3 | 101244260 | ||
| chr3:101244310
|
G | A | 5 | a0001a0004a0008others(2): Show | 220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
missense_variant | MODERATE | c.2021C>T | p.Thr674Ile | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2224/8352 | 2021/3726 | 674/1241 | chr3 | 101244310 | ||
| chr3:101244749
|
T | C | 1 | a0013 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1582A>G | p.Ile528Val | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 1785/8352 | 1582/3726 | 528/1241 | chr3 | 101244749 | ||
| chr3:101245963
|
G | C | 1 | a0005 | 2 | NA18966.hp2 NA18969.hp2 |
missense_variant | MODERATE | c.1382C>G | p.Thr461Arg | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/19 | 1585/8352 | 1382/3726 | 461/1241 | chr3 | 101245963 | ||
| chr3:101253712
|
G | A | 1 | a0004 | 2 | HG01255.hp1 HG01358.hp1 |
missense_variant | MODERATE | c.1223C>T | p.Thr408Met | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/19 | 1426/8352 | 1223/3726 | 408/1241 | chr3 | 101253712 | ||
| chr3:101253716
|
C | A | 1 | a0014 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.1219G>T | p.Ala407Ser | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/19 | 1422/8352 | 1219/3726 | 407/1241 | chr3 | 101253716 | ||
| chr3:101320333
|
TACCCAGA others(9): Show |
T | 1 | a0007 | 1 | NA18957.hp1 | frameshift_variant | HIGH | c.24_39delGAAGATTTCT others(6): Show |
p.Lys9fs | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/19 | 242/8352 | 24/3726 | 8/1241 | chr3 | 101320333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101229413
|
T | C | 1 | a0003c0009 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.3600A>G | p.Arg1200Arg | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/19 | 3803/8352 | 3600/3726 | 1200/1241 | chr3 | 101229413 | ||
| chr3:101229452
|
G | A | 1 | a0002c0013 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.3561C>T | p.Ser1187Ser | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/19 | 3764/8352 | 3561/3726 | 1187/1241 | chr3 | 101229452 | ||
| chr3:101230998
|
G | A | 14 | a0001c0001a0001c0017a0002c0003others(11): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
synonymous_variant | LOW | c.3381C>T | p.Leu1127Leu | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/19 | 3584/8352 | 3381/3726 | 1127/1241 | chr3 | 101230998 | ||
| chr3:101244408
|
T | C | 1 | a0001c0017 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1923A>G | p.Pro641Pro | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2126/8352 | 1923/3726 | 641/1241 | chr3 | 101244408 | ||
| chr3:101244423
|
A | G | 2 | a0003c0004a0003c0009 | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.1908T>C | p.Asp636Asp | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2111/8352 | 1908/3726 | 636/1241 | chr3 | 101244423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101222643
|
T | G | 1 | a0001c0001t0051 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4326A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 4326 | chr3 | 101222643 | |||||
| chr3:101222848
|
A | C | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(60): Show | 221 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*4121T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 4121 | chr3 | 101222848 | |||||
| chr3:101222995
|
T | C | 1 | a0002c0002t0093 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3974A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3974 | chr3 | 101222995 | |||||
| chr3:101223116
|
C | T | 1 | a0001c0001t0079 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3853G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3853 | chr3 | 101223116 | |||||
| chr3:101223189
|
A | T | 85 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(82): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*3780T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3780 | chr3 | 101223189 | |||||
| chr3:101223455
|
G | A | 1 | a0001c0001t0032 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3514C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3514 | chr3 | 101223455 | |||||
| chr3:101223704
|
A | T | 1 | a0001c0001t0055 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3265T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3265 | chr3 | 101223704 | |||||
| chr3:101223920
|
C | T | 3 | a0002c0003t0018a0002c0003t0056a0002c0003t0098 | 7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3049G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3049 | chr3 | 101223920 | |||||
| chr3:101224006
|
A | G | 1 | a0001c0001t0065 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2963T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2963 | chr3 | 101224006 | |||||
| chr3:101224052
|
C | T | 1 | a0001c0001t0062 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2917G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2917 | chr3 | 101224052 | |||||
| chr3:101224084
|
G | T | 2 | a0002c0003t0018a0002c0003t0098 | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2885C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2885 | chr3 | 101224084 | |||||
| chr3:101224100
|
G | A | 4 | a0001c0001t0036a0001c0001t0071a0001c0001t0074others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2869C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2869 | chr3 | 101224100 | |||||
| chr3:101224316
|
A | G | 1 | a0003c0014t0044 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2653T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2653 | chr3 | 101224316 | |||||
| chr3:101224669
|
G | A | 1 | a0001c0001t0055 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2300C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2300 | chr3 | 101224669 | |||||
| chr3:101224691
|
G | C | 6 | a0001c0001t0035a0001c0001t0065a0001c0001t0066others(3): Show | 7 | HG01884.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2278C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2278 | chr3 | 101224691 | |||||
| chr3:101224727
|
C | T | 1 | a0001c0001t0064 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2242G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2242 | chr3 | 101224727 | |||||
| chr3:101224874
|
C | T | 1 | a0001c0001t0029 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2095G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2095 | chr3 | 101224874 | |||||
| chr3:101224917
|
T | G | 1 | a0002c0003t0057 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2052 | chr3 | 101224917 | |||||
| chr3:101225015
|
C | T | 9 | a0001c0001t0030a0001c0001t0033a0001c0001t0050others(6): Show | 11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1954 | chr3 | 101225015 | |||||
| chr3:101225232
|
A | G | 14 | a0001c0001t0053a0002c0003t0002a0002c0003t0003others(11): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1737T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1737 | chr3 | 101225232 | |||||
| chr3:101225369
|
G | A | 1 | a0001c0001t0059 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1600C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1600 | chr3 | 101225369 | |||||
| chr3:101225374
|
C | T | 3 | a0002c0003t0018a0002c0003t0056a0002c0003t0098 | 7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1595G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1595 | chr3 | 101225374 | |||||
| chr3:101225380
|
T | C | 15 | a0001c0001t0053a0002c0003t0002a0002c0003t0003others(12): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1589A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1589 | chr3 | 101225380 | |||||
| chr3:101225411
|
ACACGCAC others(9): Show |
A | 84 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(81): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*1542_*1557delAATG others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1542 | chr3 | 101225411 | |||||
| chr3:101225427
|
T | A | 1 | a0001c0001t0054 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1542 | chr3 | 101225427 | |||||
| chr3:101225687
|
G | A | 5 | a0003c0004t0045a0003c0004t0046a0003c0004t0047others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1282C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1282 | chr3 | 101225687 | |||||
| chr3:101225965
|
C | T | 2 | a0001c0001t0070a0001c0001t0078 | 2 | HG01952.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1004 | chr3 | 101225965 | |||||
| chr3:101226088
|
A | G | 15 | a0001c0001t0053a0002c0003t0002a0002c0003t0003others(12): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 881 | chr3 | 101226088 | |||||
| chr3:101226123
|
A | C | 1 | a0001c0001t0052 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*846T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 846 | chr3 | 101226123 | |||||
| chr3:101226159
|
G | A | 2 | a0001c0001t0077a0002c0003t0098 | 2 | HG03453.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*810C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 810 | chr3 | 101226159 | |||||
| chr3:101226225
|
T | A | 1 | a0002c0002t0095 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 744 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTA | 3 | a0001c0001t0073a0001c0001t0100a0002c0002t0094 | 3 | HG01952.hp1 HG02717.hp2 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*742_*743dupTA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATA | 3 | a0001c0001t0007a0001c0001t0101a0002c0002t0040 | 12 | HG02148.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*740_*743dupTATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATA | 4 | a0001c0001t0012a0001c0001t0035a0001c0001t0074others(1): Show | 11 | HG02071.hp2 HG02074.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*738_*743dupTATATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0010a0001c0001t0077a0002c0002t0027others(3): Show | 14 | HG00639.hp2 HG01070.hp1 HG01169.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*736_*743dupTATATA others(2): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(3): Show |
5 | a0001c0001t0013a0001c0001t0036a0001c0001t0078others(2): Show | 11 | HG00099.hp2 HG00280.hp1 HG02040.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*734_*743dupTATATA others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(5): Show |
4 | a0001c0001t0021a0001c0001t0079a0001c0001t0080others(1): Show | 6 | HG01891.hp2 HG03139.hp1 NA18993.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*732_*743dupTATATA others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0016 | 5 | NA18950.hp1 NA18965.hp2 NA18970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*730_*743dupTATATA others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(9): Show |
3 | a0001c0001t0014a0002c0002t0089a0002c0002t0097 | 8 | HG01074.hp2 HG02080.hp1 HG03471.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*728_*743dupTATATA others(10): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0022a0002c0002t0090 | 5 | HG00621.hp1 HG01943.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*726_*743dupTATATA others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0037 | 2 | HG01261.hp2 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*724_*743dupTATATA others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0058 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*743_*744insTATATA others(26): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0030 | 2 | HG02145.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*743_*744insTATATA others(28): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTA | T | 5 | a0001c0001t0033a0001c0001t0034a0002c0002t0015others(2): Show | 12 | HG00140.hp2 HG02004.hp1 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*743delTA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 742 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATA | T | 9 | a0001c0001t0025a0001c0001t0068a0001c0001t0069others(6): Show | 17 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*740_*743delTATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 740 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATA | T | 4 | a0001c0001t0006a0001c0001t0066a0002c0002t0026others(1): Show | 14 | HG01099.hp1 HG01978.hp1 HG02148.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*738_*743delTATATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 738 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(1): Show |
T | 8 | a0001c0001t0032a0001c0001t0064a0001c0001t0065others(5): Show | 14 | HG00621.hp2 HG01256.hp2 HG01258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*736_*743delTATATA others(2): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 736 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0062a0001c0001t0063a0002c0002t0011others(2): Show | 13 | HG00280.hp2 HG00642.hp2 HG01071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*734_*743delTATATA others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 734 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(5): Show |
T | 3 | a0002c0002t0039a0002c0003t0024a0007c0008t0024 | 5 | HG00423.hp1 HG01106.hp2 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*732_*743delTATATA others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 732 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(7): Show |
T | 3 | a0002c0002t0086a0002c0003t0005a0013c0018t0005 | 10 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*730_*743delTATATA others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 730 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(9): Show |
T | 3 | a0001c0001t0059a0002c0002t0085a0002c0003t0003 | 18 | HG00140.hp1 HG00408.hp2 HG00733.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*728_*743delTATATA others(10): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 728 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(11): Show |
T | 3 | a0002c0003t0002a0002c0003t0057a0011c0012t0002 | 23 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*726_*743delTATATA others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 726 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(13): Show |
T | 3 | a0002c0003t0019a0002c0003t0056a0002c0013t0019 | 5 | HG01106.hp1 HG02922.hp2 NA18970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*724_*743delTATATA others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 724 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(15): Show |
T | 2 | a0003c0004t0047a0003c0014t0044 | 2 | HG02559.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*722_*743delTATATA others(16): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 722 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0082 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718_*743delTATATA others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 718 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(21): Show |
T | 2 | a0001c0001t0008a0001c0001t0028 | 10 | HG00642.hp1 HG01123.hp1 HG01167.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*743delTATATA others(22): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 716 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(23): Show |
T | 2 | a0002c0003t0098a0003c0009t0049 | 2 | HG01891.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*714_*743delTATATA others(24): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 714 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(25): Show |
T | 2 | a0002c0002t0084a0002c0003t0018 | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*712_*743delTATATA others(26): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 712 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(27): Show |
T | 1 | a0003c0004t0046 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710_*743delTATATA others(28): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 710 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(29): Show |
T | 2 | a0001c0001t0023a0003c0004t0045 | 4 | HG03490.hp2 HG03579.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*708_*743delTATATA others(30): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 708 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(31): Show |
T | 12 | a0001c0001t0001a0001c0001t0029a0001c0001t0043others(9): Show | 102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*706_*743delTATATA others(32): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 706 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(33): Show |
T | 2 | a0001c0001t0050a0001c0001t0051 | 2 | HG02486.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*704_*743delTATATA others(34): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 704 | chr3 | 101226225 | |||||
| chr3:101226225
|
TTATATAT others(35): Show |
T | 1 | a0002c0002t0092 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702_*743delTATATA others(36): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 702 | chr3 | 101226225 | |||||
| chr3:101226241
|
A | ATTTATAT others(65): Show |
1 | a0001c0001t0061 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727_*728insAATATA others(66): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 727 | chr3 | 101226241 | |||||
| chr3:101226241
|
A | ATTTATAT others(29): Show |
1 | a0001c0001t0060 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*727_*728insAATATA others(30): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 727 | chr3 | 101226241 | |||||
| chr3:101226243
|
A | T | 3 | a0001c0001t0030a0001c0001t0058a0001c0001t0081 | 4 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 726 | chr3 | 101226243 | |||||
| chr3:101226260
|
T | TATATATA others(27): Show |
1 | a0001c0001t0081 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*708_*709insTTATAT others(28): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 708 | chr3 | 101226260 | |||||
| chr3:101226265
|
A | G | 1 | a0001c0001t0082 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 704 | chr3 | 101226265 | |||||
| chr3:101226266
|
T | C | 1 | a0001c0001t0082 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 703 | chr3 | 101226266 | |||||
| chr3:101226305
|
A | G | 1 | a0002c0002t0083 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*664T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 664 | chr3 | 101226305 | |||||
| chr3:101226334
|
A | T | 1 | a0002c0002t0091 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 635 | chr3 | 101226334 | |||||
| chr3:101226401
|
G | T | 85 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(82): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*568C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 568 | chr3 | 101226401 | |||||
| chr3:101226523
|
C | T | 5 | a0003c0004t0045a0003c0004t0046a0003c0004t0047others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*446G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 446 | chr3 | 101226523 | |||||
| chr3:101226525
|
C | T | 4 | a0003c0004t0045a0003c0004t0046a0003c0004t0047others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*444G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 444 | chr3 | 101226525 | |||||
| chr3:101226543
|
C | T | 1 | a0001c0001t0028 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*426G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 426 | chr3 | 101226543 | |||||
| chr3:101226589
|
G | T | 95 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(92): Show | 304 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*380C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 380 | chr3 | 101226589 | |||||
| chr3:101226669
|
A | C | 1 | a0003c0014t0044 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 300 | chr3 | 101226669 | |||||
| chr3:101226709
|
T | C | 2 | a0002c0003t0018a0002c0003t0098 | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*260A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 260 | chr3 | 101226709 | |||||
| chr3:101226741
|
A | G | 1 | a0001c0001t0043 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 228 | chr3 | 101226741 | |||||
| chr3:101226819
|
G | GA | 5 | a0001c0001t0099a0001c0001t0100a0001c0001t0101others(2): Show | 5 | HG03209.hp2 NA18942.hp1 NA19057.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*149dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 149 | chr3 | 101226819 | |||||
| chr3:101226882
|
T | G | 1 | a0001c0001t0104 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 87 | chr3 | 101226882 | |||||
| chr3:101320485
|
A | G | 1 | a0002c0002t0042 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/19 | 113 | chr3 | 101320485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101227139
|
A | T | 210 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 221 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.3714-158T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227139 | ||||||
| chr3:101227140
|
T | A | 5 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3714-159A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227140 | ||||||
| chr3:101227326
|
G | A | 1 | a0002c0003t0003g0288 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3714-345C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227326 | ||||||
| chr3:101227391
|
C | G | 1 | a0002c0003t0005g0276 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3714-410G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227391 | ||||||
| chr3:101227569
|
T | C | 280 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(277): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.3714-588A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227569 | ||||||
| chr3:101227570
|
G | A | 1 | a0013c0018t0005g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3714-589C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227570 | ||||||
| chr3:101227898
|
T | G | 280 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(277): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.3713+899A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227898 | ||||||
| chr3:101227936
|
A | G | 1 | a0001c0001t0013g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3713+861T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227936 | ||||||
| chr3:101227964
|
T | C | 1 | a0001c0001t0077g0043 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3713+833A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227964 | ||||||
| chr3:101228014
|
C | T | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3713+783G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228014 | ||||||
| chr3:101228021
|
C | T | 5 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3713+776G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228021 | ||||||
| chr3:101228189
|
T | C | 1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3713+608A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228189 | ||||||
| chr3:101228367
|
A | C | 1 | a0002c0003t0003g0263 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3713+430T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228367 | ||||||
| chr3:101228412
|
G | T | 1 | a0002c0003t0002g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3713+385C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228412 | ||||||
| chr3:101228419
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3713+378T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228419 | ||||||
| chr3:101228475
|
G | A | 1 | a0002c0003t0018g0223 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3713+322C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228475 | ||||||
| chr3:101228621
|
G | A | 5 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3713+176C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228621 | ||||||
| chr3:101228730
|
G | T | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3713+67C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228730 | ||||||
| chr3:101228970
|
C | T | 1 | a0002c0003t0056g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3634-94G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101228970 | ||||||
| chr3:101229138
|
C | CA | 8 | a0002c0002t0009g0199a0002c0002t0103g0315a0002c0003t0002g0265others(5): Show | 8 | HG00673.hp1 HG01106.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3633+241dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229138 | ||||||
| chr3:101229138
|
CA | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 112 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.3633+241delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229138 | ||||||
| chr3:101229138
|
CAA | C | 110 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(107): Show | 114 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.3633+240_3633+241d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229138 | ||||||
| chr3:101229156
|
G | A | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+224C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229156 | ||||||
| chr3:101229167
|
G | A | 6 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+213C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229167 | ||||||
| chr3:101229763
|
TATC | T | 6 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3423-176_3423-174d others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101229763 | ||||||
| chr3:101230076
|
G | A | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3423-486C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230076 | ||||||
| chr3:101230156
|
A | G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3423-566T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230156 | ||||||
| chr3:101230163
|
C | T | 1 | a0002c0003t0067g0284 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3423-573G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230163 | ||||||
| chr3:101230369
|
A | G | 1 | a0002c0002t0086g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3422+588T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230369 | ||||||
| chr3:101230487
|
T | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3422+470A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230487 | ||||||
| chr3:101230491
|
T | C | 1 | a0001c0001t0020g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3422+466A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230491 | ||||||
| chr3:101230582
|
T | C | 2 | a0002c0003t0002g0283a0002c0003t0003g0285 | 2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.3422+375A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230582 | ||||||
| chr3:101230824
|
C | A | 88 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(85): Show | 92 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3422+133G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230824 | ||||||
| chr3:101230907
|
T | C | 1 | a0002c0003t0003g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3422+50A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230907 | ||||||
| chr3:101231190
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3234-45G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231190 | ||||||
| chr3:101231317
|
A | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3234-172T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231317 | ||||||
| chr3:101231335
|
C | T | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3234-190G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231335 | ||||||
| chr3:101231626
|
A | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 75 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.3234-481T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231626 | ||||||
| chr3:101231628
|
G | A | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3234-483C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231628 | ||||||
| chr3:101231831
|
T | C | 1 | a0002c0002t0015g0318 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3234-686A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231831 | ||||||
| chr3:101232223
|
A | AT | 210 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 221 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.3233+557dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232223 | ||||||
| chr3:101232223
|
A | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3233+558T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232223 | ||||||
| chr3:101232234
|
A | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3233+547T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232234 | ||||||
| chr3:101232238
|
A | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3233+543T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232238 | ||||||
| chr3:101232284
|
C | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3233+497G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232284 | ||||||
| chr3:101232330
|
C | T | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3233+451G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232330 | ||||||
| chr3:101232382
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3233+399A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232382 | ||||||
| chr3:101232461
|
C | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(206): Show | 220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3233+320G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232461 | ||||||
| chr3:101232611
|
T | C | 5 | a0001c0001t0012g0067a0001c0001t0012g0074a0001c0001t0013g0070others(2): Show | 5 | HG02080.hp2 NA18954.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3233+170A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232611 | ||||||
| chr3:101232726
|
T | C | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3233+55A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232726 | ||||||
| chr3:101232735
|
GAAATATC others(31): Show |
G | 1 | a0001c0001t0001g0122 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.3233+8_3233+45delG others(37): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232735 | ||||||
| chr3:101233231
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3023-240C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233231 | ||||||
| chr3:101233292
|
C | G | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3023-301G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233292 | ||||||
| chr3:101233336
|
T | C | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-345A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233336 | ||||||
| chr3:101233385
|
T | C | 2 | a0001c0001t0010g0019a0001c0001t0014g0005 | 3 | HG03490.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3023-394A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233385 | ||||||
| chr3:101233423
|
A | G | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-432T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233423 | ||||||
| chr3:101233446
|
G | C | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-455C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233446 | ||||||
| chr3:101233465
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3023-474G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233465 | ||||||
| chr3:101233597
|
C | G | 2 | a0002c0003t0005g0293a0002c0003t0005g0295 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3023-606G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233597 | ||||||
| chr3:101233848
|
T | C | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-857A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233848 | ||||||
| chr3:101233934
|
A | G | 1 | a0002c0003t0019g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3023-943T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233934 | ||||||
| chr3:101233981
|
A | G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-990T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233981 | ||||||
| chr3:101234273
|
G | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-1282C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234273 | ||||||
| chr3:101234368
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3023-1377A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234368 | ||||||
| chr3:101234473
|
C | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0131others(5): Show | 9 | HG02559.hp2 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3023-1482G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234473 | ||||||
| chr3:101234582
|
T | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-1591A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234582 | ||||||
| chr3:101234598
|
G | T | 1 | a0002c0003t0002g0306 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3023-1607C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234598 | ||||||
| chr3:101234681
|
A | G | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-1690T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234681 | ||||||
| chr3:101234707
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0134 | 2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3023-1716C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234707 | ||||||
| chr3:101234710
|
A | G | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-1719T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234710 | ||||||
| chr3:101234712
|
G | C | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-1721C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234712 | ||||||
| chr3:101234941
|
T | G | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-1950A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234941 | ||||||
| chr3:101234998
|
C | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0137 | 4 | HG02738.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3023-2007G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234998 | ||||||
| chr3:101235005
|
A | G | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-2014T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235005 | ||||||
| chr3:101235034
|
T | C | 5 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-2043A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235034 | ||||||
| chr3:101235090
|
C | T | 1 | a0002c0003t0056g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3023-2099G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235090 | ||||||
| chr3:101235104
|
T | A | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-2113A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235104 | ||||||
| chr3:101235210
|
T | C | 1 | a0001c0001t0022g0056 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3023-2219A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235210 | ||||||
| chr3:101235338
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3023-2347A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235338 | ||||||
| chr3:101235558
|
C | T | 3 | a0001c0001t0050g0245a0001c0001t0051g0244a0002c0003t0003g0289 | 3 | HG02258.hp1 HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3023-2567G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235558 | ||||||
| chr3:101235695
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3023-2704C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235695 | ||||||
| chr3:101235776
|
G | A | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3023-2785C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235776 | ||||||
| chr3:101235828
|
T | C | 1 | a0001c0001t0025g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3023-2837A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235828 | ||||||
| chr3:101236084
|
T | C | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-3093A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236084 | ||||||
| chr3:101236161
|
G | A | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-3170C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236161 | ||||||
| chr3:101236251
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3023-3260C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236251 | ||||||
| chr3:101236302
|
C | T | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-3311G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236302 | ||||||
| chr3:101236415
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(206): Show | 220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3023-3424C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236415 | ||||||
| chr3:101236451
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3023-3460G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236451 | ||||||
| chr3:101236460
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3023-3469A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236460 | ||||||
| chr3:101236485
|
T | C | 3 | a0001c0001t0035g0025a0001c0001t0035g0026a0008c0015t0076g0027 | 3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3023-3494A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236485 | ||||||
| chr3:101236517
|
G | T | 1 | a0014c0019t0021g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3023-3526C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236517 | ||||||
| chr3:101236530
|
G | A | 1 | a0002c0002t0017g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3023-3539C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236530 | ||||||
| chr3:101236572
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3023-3581C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236572 | ||||||
| chr3:101236674
|
T | C | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-3683A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236674 | ||||||
| chr3:101236696
|
G | A | 1 | a0001c0001t0050g0245 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3023-3705C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236696 | ||||||
| chr3:101236747
|
C | T | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3023-3756G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236747 | ||||||
| chr3:101236748
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3023-3757T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236748 | ||||||
| chr3:101236808
|
G | GTTTGTT | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-3823_3023-381 others(10): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236808 | ||||||
| chr3:101236916
|
T | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-3925A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236916 | ||||||
| chr3:101236925
|
G | A | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-3934C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236925 | ||||||
| chr3:101237013
|
C | T | 1 | a0001c0001t0013g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3023-4022G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237013 | ||||||
| chr3:101237096
|
G | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-4105C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237096 | ||||||
| chr3:101237227
|
A | G | 1 | a0002c0003t0003g0257 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3023-4236T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237227 | ||||||
| chr3:101237286
|
G | A | 11 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3023-4295C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237286 | ||||||
| chr3:101237331
|
G | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-4340C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237331 | ||||||
| chr3:101237356
|
C | G | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-4365G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237356 | ||||||
| chr3:101238179
|
T | C | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+4509A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238179 | ||||||
| chr3:101238206
|
A | G | 2 | a0005c0006t0004g0201a0005c0006t0009g0206 | 2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.3022+4482T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238206 | ||||||
| chr3:101238476
|
C | T | 3 | a0002c0002t0004g0071a0002c0002t0027g0084a0002c0002t0041g0083 | 3 | HG00438.hp2 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3022+4212G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238476 | ||||||
| chr3:101238483
|
C | T | 2 | a0001c0001t0012g0085a0001c0001t0014g0105 | 2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4205G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238483 | ||||||
| chr3:101238496
|
A | G | 2 | a0001c0001t0012g0085a0001c0001t0014g0105 | 2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4192T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238496 | ||||||
| chr3:101238498
|
C | T | 2 | a0001c0001t0012g0085a0001c0001t0014g0105 | 2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4190G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238498 | ||||||
| chr3:101238514
|
G | A | 2 | a0001c0001t0012g0085a0001c0001t0014g0105 | 2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4174C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238514 | ||||||
| chr3:101238610
|
A | T | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+4078T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238610 | ||||||
| chr3:101238816
|
G | A | 6 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3872C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238816 | ||||||
| chr3:101238837
|
T | C | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3851A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238837 | ||||||
| chr3:101238911
|
A | T | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3022+3777T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238911 | ||||||
| chr3:101238954
|
T | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3022+3734A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238954 | ||||||
| chr3:101238973
|
C | T | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3715G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238973 | ||||||
| chr3:101239174
|
GCAATCTA others(39): Show |
G | 4 | a0001c0001t0007g0001a0001c0001t0007g0054a0001c0001t0007g0055others(1): Show | 6 | NA18946.hp2 NA18947.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.3022+3468_3022+351 others(50): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239174 | ||||||
| chr3:101239175
|
C | T | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3513G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239175 | ||||||
| chr3:101239280
|
T | C | 1 | a0001c0001t0051g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3022+3408A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239280 | ||||||
| chr3:101239311
|
T | C | 1 | a0002c0003t0005g0295 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3022+3377A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239311 | ||||||
| chr3:101239410
|
C | T | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3278G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239410 | ||||||
| chr3:101239451
|
T | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3022+3237A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239451 | ||||||
| chr3:101239563
|
T | C | 1 | a0002c0002t0004g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3022+3125A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239563 | ||||||
| chr3:101239588
|
A | G | 1 | a0002c0003t0056g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3022+3100T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239588 | ||||||
| chr3:101239633
|
C | T | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3022+3055G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239633 | ||||||
| chr3:101239766
|
G | A | 2 | a0002c0002t0009g0316a0002c0002t0026g0323 | 2 | HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3022+2922C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239766 | ||||||
| chr3:101239805
|
G | T | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3022+2883C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239805 | ||||||
| chr3:101239868
|
A | G | 1 | a0002c0003t0056g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3022+2820T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239868 | ||||||
| chr3:101239915
|
G | A | 1 | a0002c0003t0003g0273 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3022+2773C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239915 | ||||||
| chr3:101239930
|
C | T | 1 | a0002c0002t0038g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3022+2758G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239930 | ||||||
| chr3:101240016
|
G | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3022+2672C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240016 | ||||||
| chr3:101240067
|
TA | T | 7 | a0001c0001t0001g0112a0001c0001t0065g0233a0003c0004t0045g0344others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3022+2620delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240067 | ||||||
| chr3:101240125
|
A | T | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3022+2563T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240125 | ||||||
| chr3:101240126
|
T | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3022+2562A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240126 | ||||||
| chr3:101240176
|
C | T | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3022+2512G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240176 | ||||||
| chr3:101240190
|
G | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3022+2498C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240190 | ||||||
| chr3:101240227
|
C | T | 7 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(4): Show | 7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3022+2461G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240227 | ||||||
| chr3:101240230
|
ACCTCAGC | A | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3022+2451_3022+245 others(11): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240230 | ||||||
| chr3:101240325
|
C | T | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3022+2363G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240325 | ||||||
| chr3:101240496
|
A | G | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3022+2192T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240496 | ||||||
| chr3:101240518
|
A | T | 1 | a0001c0001t0073g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3022+2170T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240518 | ||||||
| chr3:101240536
|
T | C | 1 | a0001c0001t0073g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3022+2152A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240536 | ||||||
| chr3:101240975
|
T | C | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+1713A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240975 | ||||||
| chr3:101241452
|
T | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3022+1236A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241452 | ||||||
| chr3:101241633
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3022+1055A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241633 | ||||||
| chr3:101241798
|
T | G | 7 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.3022+890A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241798 | ||||||
| chr3:101241833
|
G | A | 1 | a0002c0002t0092g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3022+855C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241833 | ||||||
| chr3:101242035
|
GA | G | 12 | a0001c0001t0012g0074a0001c0001t0013g0070a0001c0001t0051g0244others(9): Show | 12 | HG01891.hp1 HG02080.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.3022+652delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242035 | ||||||
| chr3:101242051
|
A | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3022+637T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242051 | ||||||
| chr3:101242315
|
A | T | 7 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(4): Show | 7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3022+373T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242315 | ||||||
| chr3:101242640
|
T | C | 1 | a0002c0002t0084g0086 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3022+48A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242640 | ||||||
| chr3:101242964
|
A | G | 1 | a0002c0003t0002g0261 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2803-57T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101242964 | ||||||
| chr3:101243061
|
C | T | 2 | a0001c0001t0036g0249a0001c0001t0080g0248 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2803-154G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243061 | ||||||
| chr3:101243239
|
G | A | 6 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2802+290C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243239 | ||||||
| chr3:101243310
|
T | G | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2802+219A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243310 | ||||||
| chr3:101243394
|
A | G | 1 | a0001c0001t0043g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2802+135T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243394 | ||||||
| chr3:101244807
|
T | G | 1 | a0001c0001t0007g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1544-20A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101244807 | ||||||
| chr3:101244917
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 105 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1544-130A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101244917 | ||||||
| chr3:101244995
|
C | T | 2 | a0002c0003t0031g0300a0002c0003t0031g0301 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1544-208G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101244995 | ||||||
| chr3:101245013
|
G | C | 1 | a0001c0001t0055g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1544-226C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245013 | ||||||
| chr3:101245040
|
G | GT | 62 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0012g0074others(59): Show | 64 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1544-254dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245040 | ||||||
| chr3:101245040
|
GT | G | 8 | a0001c0001t0014g0097a0002c0003t0056g0253a0003c0004t0045g0344others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544-254delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245040 | ||||||
| chr3:101245127
|
A | C | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1544-340T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245127 | ||||||
| chr3:101245168
|
C | T | 2 | a0002c0002t0089g0338a0002c0002t0090g0339 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1544-381G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245168 | ||||||
| chr3:101245226
|
T | C | 6 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-439A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245226 | ||||||
| chr3:101245421
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1543+381G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245421 | ||||||
| chr3:101245549
|
A | G | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543+253T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245549 | ||||||
| chr3:101245557
|
T | C | 1 | a0002c0002t0004g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1543+245A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245557 | ||||||
| chr3:101245755
|
G | A | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543+47C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245755 | ||||||
| chr3:101246388
|
A | AT | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-284dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246388 | ||||||
| chr3:101246664
|
A | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0238others(2): Show | 5 | HG01978.hp2 HG02109.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-559T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246664 | ||||||
| chr3:101246702
|
T | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1240-597A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246702 | ||||||
| chr3:101246707
|
C | T | 1 | a0001c0001t0010g0019 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1240-602G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246707 | ||||||
| chr3:101246810
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1240-705A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246810 | ||||||
| chr3:101247092
|
T | C | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-987A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247092 | ||||||
| chr3:101247097
|
T | TA | 93 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(90): Show | 97 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1240-993dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247097 | ||||||
| chr3:101247097
|
TA | T | 15 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(12): Show | 15 | HG01106.hp1 HG02055.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1240-993delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247097 | ||||||
| chr3:101247234
|
G | A | 8 | a0002c0003t0056g0253a0002c0003t0098g0243a0003c0004t0045g0344others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240-1129C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247234 | ||||||
| chr3:101247366
|
T | C | 8 | a0002c0003t0056g0253a0002c0003t0098g0243a0003c0004t0045g0344others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240-1261A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247366 | ||||||
| chr3:101247416
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0238others(1): Show | 4 | HG01978.hp2 HG02293.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-1311C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247416 | ||||||
| chr3:101247419
|
G | A | 3 | a0001c0001t0035g0025a0001c0001t0035g0026a0008c0015t0076g0027 | 3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1240-1314C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247419 | ||||||
| chr3:101247468
|
A | T | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1240-1363T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247468 | ||||||
| chr3:101247525
|
C | T | 1 | a0001c0001t0020g0060 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1240-1420G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247525 | ||||||
| chr3:101247537
|
T | C | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-1432A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247537 | ||||||
| chr3:101247602
|
TA | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1240-1498delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247602 | ||||||
| chr3:101247602
|
TAA | T | 6 | a0002c0003t0002g0283a0002c0003t0018g0219a0002c0003t0018g0220others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-1499_1240-149 others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247602 | ||||||
| chr3:101247722
|
T | C | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1240-1617A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247722 | ||||||
| chr3:101247788
|
T | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1240-1683A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247788 | ||||||
| chr3:101247952
|
C | G | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1240-1847G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247952 | ||||||
| chr3:101248090
|
A | G | 5 | a0002c0003t0002g0265a0002c0003t0002g0267a0002c0003t0003g0266others(2): Show | 5 | HG00673.hp1 HG02015.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240-1985T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248090 | ||||||
| chr3:101248098
|
A | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1240-1993T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248098 | ||||||
| chr3:101248165
|
A | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0113others(4): Show | 9 | NA18747.hp2 NA18942.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-2060T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248165 | ||||||
| chr3:101248806
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1240-2701G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248806 | ||||||
| chr3:101248856
|
C | T | 1 | a0003c0004t0047g0343 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1240-2751G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248856 | ||||||
| chr3:101249022
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1240-2917G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249022 | ||||||
| chr3:101249076
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 217 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1240-2971T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249076 | ||||||
| chr3:101249204
|
C | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 73 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1240-3099G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249204 | ||||||
| chr3:101249262
|
G | A | 13 | a0001c0001t0035g0025a0001c0001t0035g0026a0001c0001t0065g0233others(10): Show | 13 | HG01884.hp1 HG01975.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-3157C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249262 | ||||||
| chr3:101249333
|
A | C | 2 | a0001c0001t0007g0089a0002c0002t0084g0086 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1240-3228T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249333 | ||||||
| chr3:101249794
|
C | CA | 68 | a0001c0001t0006g0087a0001c0001t0036g0249a0001c0001t0036g0252others(65): Show | 70 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1240-3690dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249794 | ||||||
| chr3:101249794
|
CA | C | 14 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0035g0025others(11): Show | 14 | HG01975.hp1 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240-3690delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249794 | ||||||
| chr3:101249937
|
G | A | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1239+3759C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249937 | ||||||
| chr3:101249976
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1239+3720G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249976 | ||||||
| chr3:101250176
|
T | C | 1 | a0001c0001t0008g0078 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1239+3520A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250176 | ||||||
| chr3:101250363
|
G | T | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1239+3333C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250363 | ||||||
| chr3:101250508
|
C | T | 6 | a0002c0002t0038g0342a0002c0002t0042g0012a0002c0002t0085g0341others(3): Show | 6 | HG02615.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1239+3188G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250508 | ||||||
| chr3:101250952
|
A | G | 3 | a0002c0003t0002g0294a0002c0003t0005g0293a0002c0003t0005g0295 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1239+2744T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250952 | ||||||
| chr3:101250983
|
A | G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239+2713T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250983 | ||||||
| chr3:101251066
|
A | G | 1 | a0001c0001t0007g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1239+2630T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251066 | ||||||
| chr3:101251073
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1239+2623T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251073 | ||||||
| chr3:101251218
|
A | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(217): Show | 231 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1239+2478T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251218 | ||||||
| chr3:101251396
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 74 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1239+2300A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251396 | ||||||
| chr3:101251401
|
T | TA | 4 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0051g0244others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+2294dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251401 | ||||||
| chr3:101251435
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1239+2261T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251435 | ||||||
| chr3:101251568
|
T | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+2128A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251568 | ||||||
| chr3:101251657
|
G | T | 11 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239+2039C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251657 | ||||||
| chr3:101251925
|
G | A | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+1771C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251925 | ||||||
| chr3:101252011
|
T | A | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+1685A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252011 | ||||||
| chr3:101252033
|
C | A | 2 | a0002c0002t0009g0029a0002c0002t0009g0199 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1239+1663G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252033 | ||||||
| chr3:101252076
|
A | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(217): Show | 231 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1239+1620T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252076 | ||||||
| chr3:101252078
|
C | T | 2 | a0001c0001t0012g0085a0001c0001t0014g0105 | 2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1239+1618G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252078 | ||||||
| chr3:101252122
|
C | T | 1 | a0001c0001t0043g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1239+1574G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252122 | ||||||
| chr3:101252130
|
A | ACAGC | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+1565_1239+156 others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252130 | ||||||
| chr3:101252194
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1239+1502A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252194 | ||||||
| chr3:101252210
|
A | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239+1486T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252210 | ||||||
| chr3:101252296
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1239+1400C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252296 | ||||||
| chr3:101252337
|
C | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1239+1359G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252337 | ||||||
| chr3:101252474
|
A | G | 3 | a0002c0002t0004g0196a0002c0002t0015g0186a0002c0002t0026g0197 | 3 | NA18947.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1239+1222T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252474 | ||||||
| chr3:101252656
|
C | T | 1 | a0001c0001t0054g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1239+1040G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252656 | ||||||
| chr3:101252834
|
C | T | 1 | a0003c0004t0048g0345 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1239+862G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252834 | ||||||
| chr3:101252945
|
A | G | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+751T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252945 | ||||||
| chr3:101253085
|
G | A | 1 | a0002c0002t0039g0327 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1239+611C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253085 | ||||||
| chr3:101253106
|
A | T | 2 | a0001c0001t0033g0312a0001c0001t0033g0313 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1239+590T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253106 | ||||||
| chr3:101253234
|
G | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1239+462C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253234 | ||||||
| chr3:101253235
|
A | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1239+461T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253235 | ||||||
| chr3:101253237
|
A | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1239+459T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253237 | ||||||
| chr3:101253327
|
G | C | 1 | a0001c0001t0006g0107 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1239+369C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253327 | ||||||
| chr3:101253335
|
C | T | 3 | a0001c0001t0032g0081a0001c0001t0032g0099a0001c0001t0064g0064 | 3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1239+361G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253335 | ||||||
| chr3:101253402
|
T | C | 5 | a0002c0002t0009g0217a0002c0002t0015g0102a0006c0005t0004g0215others(2): Show | 5 | NA18747.hp1 NA18945.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+294A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253402 | ||||||
| chr3:101253460
|
C | A | 2 | a0001c0001t0012g0074a0001c0001t0013g0070 | 2 | HG02080.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1239+236G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253460 | ||||||
| chr3:101253583
|
G | A | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+113C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253583 | ||||||
| chr3:101253662
|
G | C | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+34C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253662 | ||||||
| chr3:101254014
|
A | G | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1154-233T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254014 | ||||||
| chr3:101254301
|
A | T | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-520T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254301 | ||||||
| chr3:101254396
|
T | C | 3 | a0001c0001t0013g0032a0001c0001t0013g0065a0001c0001t0020g0066 | 3 | HG00280.hp1 HG02004.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1154-615A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254396 | ||||||
| chr3:101254457
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1154-676A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254457 | ||||||
| chr3:101254613
|
A | G | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-832T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254613 | ||||||
| chr3:101254703
|
A | C | 1 | a0002c0002t0017g0213 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1154-922T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254703 | ||||||
| chr3:101254838
|
C | T | 1 | a0002c0002t0092g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1154-1057G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254838 | ||||||
| chr3:101254874
|
G | A | 1 | a0001c0001t0034g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1154-1093C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254874 | ||||||
| chr3:101255130
|
G | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1154-1349C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255130 | ||||||
| chr3:101255174
|
A | C | 1 | a0001c0001t0014g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1154-1393T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255174 | ||||||
| chr3:101255280
|
T | G | 1 | a0001c0001t0012g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1154-1499A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255280 | ||||||
| chr3:101255515
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1154-1734C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255515 | ||||||
| chr3:101255547
|
G | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0137 | 4 | HG02738.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1766C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255547 | ||||||
| chr3:101255612
|
C | T | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-1831G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255612 | ||||||
| chr3:101255779
|
C | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1153+1750G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255779 | ||||||
| chr3:101255886
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1153+1643A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255886 | ||||||
| chr3:101255895
|
T | C | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+1634A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255895 | ||||||
| chr3:101255918
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0028others(14): Show | 19 | HG00597.hp1 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1153+1611A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255918 | ||||||
| chr3:101255988
|
T | TA | 6 | a0002c0002t0038g0342a0002c0002t0042g0012a0002c0002t0085g0341others(3): Show | 6 | HG02615.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1540dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255988 | ||||||
| chr3:101255988
|
TA | T | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+1540delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255988 | ||||||
| chr3:101255998
|
G | A | 1 | a0001c0001t0051g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+1531C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255998 | ||||||
| chr3:101256002
|
G | A | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1153+1527C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256002 | ||||||
| chr3:101256064
|
AAAAAG | A | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1153+1460_1153+146 others(9): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256064 | ||||||
| chr3:101256075
|
AAAAGAAA others(28): Show |
A | 1 | a0001c0001t0101g0127 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1153+1419_1153+145 others(39): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256075 | ||||||
| chr3:101256080
|
AAAAGAAA others(11): Show |
A | 1 | a0001c0001t0001g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1153+1431_1153+144 others(22): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256080 | ||||||
| chr3:101256114
|
G | A | 2 | a0001c0001t0001g0165a0009c0016t0001g0167 | 2 | HG01175.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1153+1415C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256114 | ||||||
| chr3:101256114
|
GA | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0146 | 3 | NA18965.hp1 NA19066.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1153+1414delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256114 | ||||||
| chr3:101256116
|
A | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0170a0009c0016t0001g0167 | 3 | HG01175.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1153+1413T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256116 | ||||||
| chr3:101256122
|
A | G | 2 | a0001c0001t0001g0165a0009c0016t0001g0167 | 2 | HG01175.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1153+1407T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256122 | ||||||
| chr3:101256126
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0170a0009c0016t0001g0167 | 3 | HG01175.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1153+1403C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256126 | ||||||
| chr3:101256132
|
GAAAGAAA others(6): Show |
G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1384_1153+139 others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256132 | ||||||
| chr3:101256144
|
G | A | 3 | a0002c0002t0084g0086a0003c0004t0045g0344a0009c0016t0001g0167 | 3 | HG03225.hp1 HG03491.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1153+1385C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256144 | ||||||
| chr3:101256144
|
G | GA | 2 | a0001c0001t0001g0009a0003c0004t0047g0343 | 3 | HG02559.hp1 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1153+1384dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256144 | ||||||
| chr3:101256145
|
A | AAAAG | 68 | a0001c0001t0001g0090a0001c0001t0001g0130a0001c0001t0001g0139others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1153+1380_1153+138 others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAAGAAA others(1): Show |
37 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0153others(34): Show | 37 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1153+1376_1153+138 others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAAGAAA others(5): Show |
18 | a0001c0001t0001g0113a0001c0001t0001g0132a0001c0001t0001g0166others(15): Show | 19 | HG00642.hp1 HG01167.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1153+1372_1153+138 others(16): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0012g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1153+1368_1153+138 others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAG | 3 | a0001c0001t0001g0165a0001c0001t0001g0170a0001c0001t0037g0073 | 3 | HG01175.hp1 NA18978.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1153+1383_1153+138 others(7): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAGAAAG others(4): Show |
1 | a0002c0003t0002g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAGAAAG others(8): Show |
1 | a0002c0002t0026g0323 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(19): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAAGAAGA others(7): Show |
1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(18): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0025g0058 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
A | G | 2 | a0002c0002t0084g0086a0009c0016t0001g0167 | 2 | HG03225.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1153+1384T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
AAAAG | A | 55 | a0001c0001t0001g0010a0001c0001t0001g0112a0001c0001t0001g0114others(52): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1153+1380_1153+138 others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
AAAAGAAA others(1): Show |
A | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0018others(24): Show | 29 | HG00099.hp2 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153+1376_1153+138 others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
AAAAGAAA others(5): Show |
A | 17 | a0001c0001t0001g0101a0001c0001t0001g0118a0001c0001t0001g0142others(14): Show | 17 | HG00621.hp1 HG00639.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1153+1372_1153+138 others(16): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
AAAAGAAA others(9): Show |
A | 1 | a0001c0001t0016g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1153+1368_1153+138 others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
AAAAGAAA others(13): Show |
A | 2 | a0001c0001t0001g0100a0001c0001t0013g0070 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1153+1364_1153+138 others(24): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256145
|
AAAAGAAA others(25): Show |
A | 1 | a0001c0001t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1153+1352_1153+138 others(36): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | ||||||
| chr3:101256165
|
GAAAGAAA others(4): Show |
G | 1 | a0002c0003t0002g0267 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1153+1353_1153+136 others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256165 | ||||||
| chr3:101256172
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1153+1357T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256172 | ||||||
| chr3:101256189
|
G | GAAAGAAA others(22): Show |
1 | a0001c0001t0051g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+1311_1153+133 others(33): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256189 | ||||||
| chr3:101256193
|
G | GAAAGAAA others(6): Show |
1 | a0001c0001t0050g0245 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1153+1323_1153+133 others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256193 | ||||||
| chr3:101256208
|
A | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1321T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256208 | ||||||
| chr3:101256212
|
A | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1317T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256212 | ||||||
| chr3:101256216
|
A | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1313T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256216 | ||||||
| chr3:101256217
|
G | A | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1312C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | ||||||
| chr3:101256217
|
G | GAAAGAAA others(3): Show |
1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1153+1311_1153+131 others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | ||||||
| chr3:101256217
|
G | GAAAGAAA others(27): Show |
1 | a0002c0003t0056g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1153+1311_1153+131 others(38): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | ||||||
| chr3:101256217
|
G | GAAAGAAA others(39): Show |
1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1153+1311_1153+131 others(50): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | ||||||
| chr3:101256217
|
G | GAACGAAC others(1): Show |
4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+1311_1153+131 others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | ||||||
| chr3:101256218
|
A | AAAGAAAG others(4): Show |
1 | a0002c0003t0003g0263 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1153+1310_1153+131 others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256218 | ||||||
| chr3:101256218
|
A | AAAGAAAG others(12): Show |
1 | a0002c0002t0009g0316 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1153+1310_1153+131 others(23): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256218 | ||||||
| chr3:101256263
|
T | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1266A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256263 | ||||||
| chr3:101256449
|
C | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(216): Show | 230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1153+1080G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256449 | ||||||
| chr3:101256598
|
C | G | 6 | a0001c0001t0008g0078a0001c0001t0010g0019a0001c0001t0010g0079others(3): Show | 7 | HG00741.hp2 HG01123.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153+931G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256598 | ||||||
| chr3:101256600
|
G | C | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+929C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256600 | ||||||
| chr3:101256710
|
A | T | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+819T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256710 | ||||||
| chr3:101256751
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1153+778G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256751 | ||||||
| chr3:101256753
|
C | T | 2 | a0001c0001t0033g0312a0001c0001t0033g0313 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1153+776G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256753 | ||||||
| chr3:101256988
|
T | C | 1 | a0001c0001t0014g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1153+541A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256988 | ||||||
| chr3:101257033
|
A | G | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+496T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257033 | ||||||
| chr3:101257146
|
A | G | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+383T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257146 | ||||||
| chr3:101257231
|
A | C | 1 | a0001c0001t0033g0312 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1153+298T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257231 | ||||||
| chr3:101257349
|
G | A | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+180C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257349 | ||||||
| chr3:101257370
|
A | T | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+159T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257370 | ||||||
| chr3:101257375
|
C | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(216): Show | 230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1153+154G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257375 | ||||||
| chr3:101257854
|
A | G | 3 | a0002c0003t0002g0261a0002c0003t0003g0259a0002c0003t0003g0260 | 3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.909-81T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101257854 | ||||||
| chr3:101257911
|
G | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(285): Show | 301 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.909-138C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101257911 | ||||||
| chr3:101257922
|
A | C | 8 | a0002c0003t0056g0253a0002c0003t0098g0243a0003c0004t0045g0344others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-149T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101257922 | ||||||
| chr3:101258394
|
T | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(216): Show | 230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.909-621A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258394 | ||||||
| chr3:101258566
|
C | T | 276 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(273): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.909-793G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258566 | ||||||
| chr3:101258653
|
T | C | 3 | a0001c0001t0012g0110a0001c0001t0070g0109a0001c0001t0078g0111 | 3 | HG01952.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.909-880A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258653 | ||||||
| chr3:101258784
|
A | T | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-1011T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258784 | ||||||
| chr3:101259063
|
C | T | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.909-1290G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259063 | ||||||
| chr3:101259295
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.909-1522C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259295 | ||||||
| chr3:101259436
|
C | T | 8 | a0002c0003t0056g0253a0002c0003t0098g0243a0003c0004t0045g0344others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-1663G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259436 | ||||||
| chr3:101259444
|
C | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.909-1671G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259444 | ||||||
| chr3:101259535
|
T | C | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1762A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259535 | ||||||
| chr3:101259598
|
C | T | 38 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(35): Show | 39 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.909-1825G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259598 | ||||||
| chr3:101259701
|
G | A | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-1928C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259701 | ||||||
| chr3:101259951
|
G | C | 58 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.909-2178C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259951 | ||||||
| chr3:101260106
|
C | T | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-2333G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260106 | ||||||
| chr3:101260141
|
T | C | 65 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(62): Show | 67 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.909-2368A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260141 | ||||||
| chr3:101260176
|
G | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.909-2403C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260176 | ||||||
| chr3:101260301
|
G | A | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2528C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260301 | ||||||
| chr3:101260412
|
A | C | 93 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(90): Show | 97 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.909-2639T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260412 | ||||||
| chr3:101260633
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.909-2860T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260633 | ||||||
| chr3:101260681
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.909-2908G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260681 | ||||||
| chr3:101260685
|
C | T | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2912G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260685 | ||||||
| chr3:101260821
|
A | G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.909-3048T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260821 | ||||||
| chr3:101260982
|
A | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(216): Show | 230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.909-3209T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260982 | ||||||
| chr3:101261207
|
G | A | 1 | a0002c0003t0003g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.909-3434C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261207 | ||||||
| chr3:101261292
|
G | T | 1 | a0001c0001t0025g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.909-3519C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261292 | ||||||
| chr3:101261334
|
A | C | 1 | a0002c0003t0002g0302 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909-3561T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261334 | ||||||
| chr3:101261393
|
C | T | 11 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.909-3620G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261393 | ||||||
| chr3:101261467
|
A | G | 65 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(62): Show | 67 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.909-3694T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261467 | ||||||
| chr3:101261500
|
T | G | 8 | a0002c0003t0056g0253a0002c0003t0098g0243a0003c0004t0045g0344others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-3727A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261500 | ||||||
| chr3:101261558
|
A | G | 1 | a0001c0001t0013g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.909-3785T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261558 | ||||||
| chr3:101261697
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-3924A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261697 | ||||||
| chr3:101261800
|
C | G | 1 | a0001c0001t0012g0067 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.909-4027G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261800 | ||||||
| chr3:101261802
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.909-4029T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261802 | ||||||
| chr3:101261863
|
G | A | 2 | a0001c0001t0001g0254a0002c0002t0086g0094 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.909-4090C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261863 | ||||||
| chr3:101261962
|
C | T | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-4189G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261962 | ||||||
| chr3:101262005
|
A | G | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.909-4232T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262005 | ||||||
| chr3:101262345
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.909-4572A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262345 | ||||||
| chr3:101262389
|
T | G | 1 | a0001c0001t0065g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.909-4616A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262389 | ||||||
| chr3:101262466
|
T | G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.909-4693A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262466 | ||||||
| chr3:101262582
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(216): Show | 230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.909-4809T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262582 | ||||||
| chr3:101262633
|
AAT | A | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-4862_909-4861d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262633 | ||||||
| chr3:101262637
|
A | G | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-4864T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262637 | ||||||
| chr3:101262711
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+4800G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262711 | ||||||
| chr3:101262770
|
C | CA | 59 | a0001c0001t0001g0130a0001c0001t0043g0148a0002c0003t0002g0003others(56): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.908+4740dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262770 | ||||||
| chr3:101262770
|
C | CAA | 6 | a0002c0003t0002g0304a0002c0003t0056g0253a0002c0003t0075g0268others(3): Show | 6 | HG00639.hp2 HG01993.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+4739_908+4740d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262770 | ||||||
| chr3:101262770
|
CA | C | 16 | a0001c0001t0008g0078a0001c0001t0010g0019a0001c0001t0010g0079others(13): Show | 17 | HG01123.hp1 HG01884.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.908+4740delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262770 | ||||||
| chr3:101262784
|
C | A | 11 | a0001c0001t0060g0337a0001c0001t0061g0332a0002c0002t0011g0322others(8): Show | 11 | HG00280.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.908+4727G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262784 | ||||||
| chr3:101262896
|
G | A | 2 | a0001c0001t0006g0069a0001c0001t0016g0075 | 2 | NA18939.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.908+4615C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262896 | ||||||
| chr3:101262956
|
G | A | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+4555C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262956 | ||||||
| chr3:101263088
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.908+4423T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263088 | ||||||
| chr3:101263115
|
C | A | 4 | a0001c0001t0007g0001a0001c0001t0007g0054a0001c0001t0007g0055others(1): Show | 6 | NA18946.hp2 NA18947.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+4396G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263115 | ||||||
| chr3:101263146
|
A | G | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+4365T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263146 | ||||||
| chr3:101263334
|
T | G | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.908+4177A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263334 | ||||||
| chr3:101263659
|
C | G | 1 | a0001c0001t0063g0080 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.908+3852G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263659 | ||||||
| chr3:101263681
|
A | C | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+3830T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263681 | ||||||
| chr3:101263833
|
A | G | 1 | a0002c0003t0003g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.908+3678T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263833 | ||||||
| chr3:101263857
|
C | CA | 7 | a0001c0001t0008g0078a0001c0001t0010g0019a0001c0001t0010g0079others(4): Show | 8 | HG01123.hp1 HG01943.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+3653dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263857 | ||||||
| chr3:101263857
|
CA | C | 9 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0006g0069others(6): Show | 9 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.908+3653delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263857 | ||||||
| chr3:101263876
|
G | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.908+3635C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263876 | ||||||
| chr3:101264251
|
T | C | 1 | a0001c0001t0012g0074 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.908+3260A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264251 | ||||||
| chr3:101264277
|
A | C | 1 | a0012c0010t0017g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.908+3234T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264277 | ||||||
| chr3:101264330
|
G | A | 1 | a0001c0001t0007g0038 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.908+3181C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264330 | ||||||
| chr3:101264610
|
T | C | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+2901A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264610 | ||||||
| chr3:101264969
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0028g0051others(1): Show | 4 | HG01515.hp2 HG01517.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+2542C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264969 | ||||||
| chr3:101265208
|
T | C | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.908+2303A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265208 | ||||||
| chr3:101265355
|
G | A | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+2156C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265355 | ||||||
| chr3:101265360
|
A | G | 1 | a0001c0001t0022g0056 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.908+2151T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265360 | ||||||
| chr3:101265761
|
G | A | 2 | a0001c0001t0021g0031a0001c0001t0025g0106 | 2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.908+1750C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265761 | ||||||
| chr3:101265767
|
C | T | 6 | a0001c0001t0008g0006a0001c0001t0008g0033a0001c0001t0008g0034others(3): Show | 7 | HG00642.hp1 HG01167.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.908+1744G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265767 | ||||||
| chr3:101265775
|
G | A | 7 | a0002c0003t0056g0253a0003c0004t0045g0344a0003c0004t0046g0330others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1736C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265775 | ||||||
| chr3:101266102
|
G | A | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.908+1409C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266102 | ||||||
| chr3:101266559
|
T | C | 8 | a0002c0003t0056g0253a0002c0003t0098g0243a0003c0004t0045g0344others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+952A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266559 | ||||||
| chr3:101266580
|
T | C | 3 | a0001c0001t0013g0024a0001c0001t0014g0023a0001c0001t0020g0021 | 3 | NA18957.hp2 NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.908+931A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266580 | ||||||
| chr3:101266853
|
G | A | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.908+658C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266853 | ||||||
| chr3:101266863
|
C | T | 1 | a0001c0001t0037g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.908+648G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266863 | ||||||
| chr3:101267133
|
A | G | 1 | a0002c0003t0002g0271 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.908+378T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267133 | ||||||
| chr3:101267300
|
T | A | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.908+211A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267300 | ||||||
| chr3:101267353
|
T | C | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.908+158A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267353 | ||||||
| chr3:101267444
|
A | G | 1 | a0001c0001t0054g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.908+67T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267444 | ||||||
| chr3:101267477
|
T | G | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+34A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267477 | ||||||
| chr3:101267612
|
C | T | 18 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(15): Show | 18 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.888-81G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267612 | ||||||
| chr3:101267689
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.888-158C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267689 | ||||||
| chr3:101267810
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.888-279T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267810 | ||||||
| chr3:101267858
|
C | CT | 209 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(206): Show | 220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.888-328dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267858 | ||||||
| chr3:101267872
|
A | G | 1 | a0001c0001t0068g0311 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.888-341T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267872 | ||||||
| chr3:101267934
|
G | A | 18 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(15): Show | 18 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.888-403C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267934 | ||||||
| chr3:101267968
|
C | A | 4 | a0003c0004t0045g0344a0003c0004t0046g0330a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.888-437G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267968 | ||||||
| chr3:101268135
|
T | C | 9 | a0002c0003t0002g0290a0002c0003t0002g0292a0002c0003t0002g0294others(6): Show | 9 | HG00733.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.888-604A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268135 | ||||||
| chr3:101268312
|
C | T | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.888-781G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268312 | ||||||
| chr3:101268415
|
C | T | 5 | a0001c0001t0008g0078a0001c0001t0010g0019a0001c0001t0010g0079others(2): Show | 6 | HG01123.hp1 HG01943.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-884G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268415 | ||||||
| chr3:101268620
|
C | CAT | 292 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(289): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.887+893_887+894dup others(2): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268620 | ||||||
| chr3:101268620
|
C | CATAT | 22 | a0001c0001t0008g0033a0001c0001t0008g0078a0001c0001t0010g0019others(19): Show | 23 | HG00438.hp2 HG01123.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.887+891_887+894dup others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268620 | ||||||
| chr3:101268675
|
T | C | 11 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.887+840A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268675 | ||||||
| chr3:101268787
|
G | A | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.887+728C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268787 | ||||||
| chr3:101268937
|
G | C | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.887+578C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268937 | ||||||
| chr3:101269003
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.887+512T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269003 | ||||||
| chr3:101269134
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.887+381T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269134 | ||||||
| chr3:101269147
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.887+368G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269147 | ||||||
| chr3:101269187
|
C | T | 17 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(14): Show | 17 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.887+328G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269187 | ||||||
| chr3:101269201
|
C | A | 2 | a0002c0003t0002g0302a0002c0003t0002g0303 | 2 | HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.887+314G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269201 | ||||||
| chr3:101269204
|
G | A | 1 | a0002c0002t0038g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.887+311C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269204 | ||||||
| chr3:101269209
|
C | CCTTCAGG | 320 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.887+305_887+306ins others(7): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269209 | ||||||
| chr3:101269260
|
G | A | 2 | a0001c0001t0023g0163a0001c0001t0023g0169 | 2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.887+255C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269260 | ||||||
| chr3:101269434
|
A | G | 1 | a0001c0001t0065g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.887+81T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269434 | ||||||
| chr3:101269785
|
C | T | 17 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(14): Show | 17 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-212G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269785 | ||||||
| chr3:101269843
|
G | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.829-270C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269843 | ||||||
| chr3:101269872
|
T | C | 5 | a0002c0003t0002g0265a0002c0003t0002g0267a0002c0003t0003g0266others(2): Show | 5 | HG00673.hp1 HG02015.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-299A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269872 | ||||||
| chr3:101269926
|
C | CT | 68 | a0001c0001t0001g0123a0001c0001t0001g0165a0001c0001t0001g0246others(65): Show | 71 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.829-354dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269926 | ||||||
| chr3:101269926
|
CT | C | 8 | a0001c0001t0001g0101a0001c0001t0001g0147a0001c0001t0001g0178others(5): Show | 8 | HG01975.hp2 HG02280.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-354delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269926 | ||||||
| chr3:101269926
|
CTTTTTTT others(5): Show |
C | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829-365_829-354del others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269926 | ||||||
| chr3:101269952
|
A | T | 1 | a0002c0002t0017g0198 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.829-379T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269952 | ||||||
| chr3:101269979
|
G | A | 3 | a0001c0001t0066g0231a0001c0001t0069g0229a0001c0001t0072g0230 | 3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.829-406C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269979 | ||||||
| chr3:101270011
|
A | C | 14 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.829-438T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270011 | ||||||
| chr3:101270032
|
G | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0023g0152others(1): Show | 4 | HG02027.hp2 HG02071.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-459C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270032 | ||||||
| chr3:101270238
|
A | T | 17 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(14): Show | 17 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-665T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270238 | ||||||
| chr3:101270268
|
C | A | 1 | a0003c0004t0048g0345 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829-695G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270268 | ||||||
| chr3:101270351
|
A | G | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829-778T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270351 | ||||||
| chr3:101270544
|
A | C | 3 | a0001c0001t0066g0231a0001c0001t0069g0229a0001c0001t0072g0230 | 3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.829-971T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270544 | ||||||
| chr3:101270573
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.829-1000C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270573 | ||||||
| chr3:101270633
|
C | T | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.829-1060G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270633 | ||||||
| chr3:101270663
|
GGTGGTGG others(9): Show |
G | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.829-1106_829-1091d others(18): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270663 | ||||||
| chr3:101270785
|
C | T | 4 | a0001c0001t0036g0252a0001c0001t0071g0251a0001c0001t0074g0250others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1212G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270785 | ||||||
| chr3:101270799
|
A | T | 1 | a0001c0001t0063g0080 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.829-1226T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270799 | ||||||
| chr3:101270953
|
C | T | 9 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(6): Show | 9 | HG00280.hp1 HG01978.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-1380G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270953 | ||||||
| chr3:101270959
|
A | G | 14 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.829-1386T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270959 | ||||||
| chr3:101270997
|
A | G | 3 | a0001c0001t0013g0032a0001c0001t0013g0065a0001c0001t0020g0066 | 3 | HG00280.hp1 HG02004.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.829-1424T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270997 | ||||||
| chr3:101271121
|
A | C | 15 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(12): Show | 15 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.829-1548T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271121 | ||||||
| chr3:101271133
|
C | T | 12 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.829-1560G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271133 | ||||||
| chr3:101271144
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829-1571C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271144 | ||||||
| chr3:101271403
|
T | C | 1 | a0001c0001t0062g0057 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.829-1830A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271403 | ||||||
| chr3:101271419
|
G | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.829-1846C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271419 | ||||||
| chr3:101271630
|
G | C | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1951C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271630 | ||||||
| chr3:101271920
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1661C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271920 | ||||||
| chr3:101272050
|
C | A | 12 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.828+1531G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272050 | ||||||
| chr3:101272055
|
T | C | 1 | a0001c0001t0008g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.828+1526A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272055 | ||||||
| chr3:101272099
|
G | GCA | 5 | a0002c0002t0038g0342a0002c0002t0085g0341a0002c0002t0087g0340others(2): Show | 5 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+1480_828+1481d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272099 | ||||||
| chr3:101272099
|
GCA | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(311): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.828+1480_828+1481d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272099 | ||||||
| chr3:101272116
|
C | T | 1 | a0003c0004t0048g0345 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.828+1465G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272116 | ||||||
| chr3:101272118
|
C | T | 2 | a0003c0004t0045g0344a0003c0004t0047g0343 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1463G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272118 | ||||||
| chr3:101272122
|
T | C | 2 | a0003c0004t0045g0344a0003c0004t0047g0343 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1459A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272122 | ||||||
| chr3:101272312
|
G | C | 1 | a0001c0001t0051g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.828+1269C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272312 | ||||||
| chr3:101272330
|
G | A | 15 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(12): Show | 15 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.828+1251C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272330 | ||||||
| chr3:101272591
|
C | G | 1 | a0010c0011t0004g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.828+990G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272591 | ||||||
| chr3:101272696
|
T | C | 12 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.828+885A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272696 | ||||||
| chr3:101272702
|
G | T | 96 | a0001c0001t0001g0090a0001c0001t0001g0246a0001c0001t0001g0247others(93): Show | 100 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.828+879C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272702 | ||||||
| chr3:101272870
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+711C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272870 | ||||||
| chr3:101273259
|
G | A | 3 | a0001c0001t0012g0074a0001c0001t0013g0070a0001c0001t0016g0092 | 3 | HG02080.hp2 NA18954.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.828+322C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273259 | ||||||
| chr3:101273299
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.828+282T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273299 | ||||||
| chr3:101273311
|
T | C | 1 | a0002c0002t0042g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.828+270A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273311 | ||||||
| chr3:101273541
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.828+40G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273541 | ||||||
| chr3:101273563
|
T | TG | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+17_828+18insC | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273563 | ||||||
| chr3:101273564
|
T | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.828+17A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273564 | ||||||
| chr3:101273922
|
G | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667-180C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101273922 | ||||||
| chr3:101273923
|
A | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667-181T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101273923 | ||||||
| chr3:101274218
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.667-476T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274218 | ||||||
| chr3:101274309
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.667-567C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274309 | ||||||
| chr3:101274480
|
C | T | 16 | a0001c0001t0001g0139a0001c0001t0030g0335a0001c0001t0030g0336others(13): Show | 16 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.667-738G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274480 | ||||||
| chr3:101274626
|
C | T | 15 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(12): Show | 15 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-884G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274626 | ||||||
| chr3:101274666
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.667-924C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274666 | ||||||
| chr3:101274689
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667-947G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274689 | ||||||
| chr3:101274776
|
G | A | 3 | a0001c0001t0016g0103a0001c0001t0022g0095a0001c0001t0059g0039 | 3 | NA18959.hp1 NA19066.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.666+887C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274776 | ||||||
| chr3:101274854
|
G | A | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.666+809C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274854 | ||||||
| chr3:101275063
|
TA | T | 23 | a0001c0001t0010g0256a0001c0001t0012g0074a0001c0001t0030g0335others(20): Show | 23 | HG00639.hp2 HG02055.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.666+599delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275063 | ||||||
| chr3:101275207
|
C | G | 320 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.666+456G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275207 | ||||||
| chr3:101275269
|
A | G | 1 | a0001c0001t0025g0058 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.666+394T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275269 | ||||||
| chr3:101275341
|
A | G | 12 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.666+322T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275341 | ||||||
| chr3:101275476
|
G | A | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666+187C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275476 | ||||||
| chr3:101275504
|
T | A | 1 | a0001c0001t0043g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.666+159A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275504 | ||||||
| chr3:101275533
|
T | C | 58 | a0001c0001t0036g0249a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.666+130A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275533 | ||||||
| chr3:101275653
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.666+10G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275653 | ||||||
| chr3:101275802
|
C | T | 1 | a0002c0002t0017g0198 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.584-57G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101275802 | ||||||
| chr3:101275837
|
T | G | 1 | a0001c0001t0007g0055 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.584-92A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101275837 | ||||||
| chr3:101275873
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.584-128G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101275873 | ||||||
| chr3:101276104
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.584-359A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276104 | ||||||
| chr3:101276320
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.583+344C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276320 | ||||||
| chr3:101276323
|
C | T | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.583+341G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276323 | ||||||
| chr3:101276356
|
C | T | 1 | a0001c0001t0020g0021 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.583+308G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276356 | ||||||
| chr3:101276858
|
T | A | 1 | a0001c0001t0055g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.534-145A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101276858 | ||||||
| chr3:101276927
|
T | C | 1 | a0001c0001t0010g0019 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.534-214A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101276927 | ||||||
| chr3:101277170
|
G | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-457C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277170 | ||||||
| chr3:101277251
|
G | T | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.534-538C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277251 | ||||||
| chr3:101277310
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.534-597A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277310 | ||||||
| chr3:101277467
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-754G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277467 | ||||||
| chr3:101277469
|
A | T | 1 | a0002c0002t0083g0320 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.534-756T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277469 | ||||||
| chr3:101277567
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.534-854A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277567 | ||||||
| chr3:101277728
|
A | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-1015T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277728 | ||||||
| chr3:101277785
|
T | C | 1 | a0002c0003t0002g0299 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.534-1072A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277785 | ||||||
| chr3:101277826
|
T | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-1113A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277826 | ||||||
| chr3:101277953
|
A | G | 3 | a0002c0003t0002g0261a0002c0003t0003g0259a0002c0003t0003g0260 | 3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.534-1240T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277953 | ||||||
| chr3:101278001
|
CA | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-1289delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278001 | ||||||
| chr3:101278061
|
C | T | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-1348G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278061 | ||||||
| chr3:101278327
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-1614C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278327 | ||||||
| chr3:101278331
|
C | G | 3 | a0001c0001t0012g0110a0001c0001t0070g0109a0001c0001t0078g0111 | 3 | HG01952.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.534-1618G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278331 | ||||||
| chr3:101278378
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.534-1665A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278378 | ||||||
| chr3:101278452
|
T | G | 3 | a0001c0001t0066g0231a0001c0001t0069g0229a0001c0001t0072g0230 | 3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.534-1739A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278452 | ||||||
| chr3:101278713
|
AC | A | 4 | a0001c0001t0043g0148a0003c0004t0045g0344a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2001delG | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278713 | ||||||
| chr3:101278714
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.534-2001G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278714 | ||||||
| chr3:101278902
|
A | T | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2189T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278902 | ||||||
| chr3:101278937
|
T | C | 1 | a0002c0002t0027g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.534-2224A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278937 | ||||||
| chr3:101278970
|
G | C | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-2257C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278970 | ||||||
| chr3:101279026
|
A | T | 2 | a0002c0002t0009g0029a0002c0002t0009g0199 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.534-2313T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279026 | ||||||
| chr3:101279088
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-2375G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279088 | ||||||
| chr3:101279158
|
TA | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-2446delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279158 | ||||||
| chr3:101279388
|
A | C | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2675T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279388 | ||||||
| chr3:101279417
|
A | T | 3 | a0001c0001t0012g0076a0001c0001t0013g0047a0001c0001t0025g0058 | 3 | HG02040.hp2 HG02071.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.534-2704T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279417 | ||||||
| chr3:101279569
|
T | C | 16 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(13): Show | 16 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-2856A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279569 | ||||||
| chr3:101279888
|
C | T | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-3175G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279888 | ||||||
| chr3:101280018
|
T | C | 4 | a0002c0002t0027g0228a0003c0004t0045g0344a0003c0004t0047g0343others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-3305A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280018 | ||||||
| chr3:101280207
|
C | A | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.534-3494G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280207 | ||||||
| chr3:101280331
|
G | A | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-3618C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280331 | ||||||
| chr3:101280498
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-3785C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280498 | ||||||
| chr3:101280823
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.534-4110G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280823 | ||||||
| chr3:101280825
|
T | C | 92 | a0001c0001t0001g0090a0001c0001t0006g0014a0001c0001t0006g0015others(89): Show | 96 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.534-4112A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280825 | ||||||
| chr3:101280872
|
G | A | 39 | a0001c0001t0065g0233a0002c0002t0004g0196a0002c0002t0004g0203others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.534-4159C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280872 | ||||||
| chr3:101280930
|
C | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-4217G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280930 | ||||||
| chr3:101280936
|
G | A | 1 | a0001c0001t0055g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.534-4223C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280936 | ||||||
| chr3:101280946
|
CA | C | 51 | a0001c0001t0035g0025a0001c0001t0035g0026a0001c0001t0065g0233others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.534-4234delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280946 | ||||||
| chr3:101280956
|
A | C | 16 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(13): Show | 16 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-4243T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280956 | ||||||
| chr3:101280987
|
TATTCTCA others(6): Show |
T | 1 | a0002c0002t0083g0320 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.534-4287_534-4275d others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280987 | ||||||
| chr3:101280995
|
A | G | 57 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-4282T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280995 | ||||||
| chr3:101281179
|
G | T | 2 | a0002c0002t0009g0316a0002c0002t0026g0323 | 2 | HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.534-4466C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281179 | ||||||
| chr3:101281445
|
G | A | 1 | a0001c0001t0007g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.534-4732C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281445 | ||||||
| chr3:101281470
|
T | C | 16 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(13): Show | 16 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-4757A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281470 | ||||||
| chr3:101281621
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0135a0001c0001t0001g0146others(4): Show | 8 | NA18939.hp1 NA18941.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-4908C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281621 | ||||||
| chr3:101281633
|
T | A | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.534-4920A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281633 | ||||||
| chr3:101281789
|
G | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-5076C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281789 | ||||||
| chr3:101281811
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-5098C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281811 | ||||||
| chr3:101281812
|
C | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-5099G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281812 | ||||||
| chr3:101282082
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534-5369T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282082 | ||||||
| chr3:101282107
|
T | G | 13 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.534-5394A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282107 | ||||||
| chr3:101282122
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.534-5409A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282122 | ||||||
| chr3:101282123
|
G | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.534-5410C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282123 | ||||||
| chr3:101282130
|
A | G | 1 | a0002c0002t0017g0198 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.534-5417T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282130 | ||||||
| chr3:101282220
|
G | A | 1 | a0001c0001t0023g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.534-5507C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282220 | ||||||
| chr3:101282259
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-5546C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282259 | ||||||
| chr3:101282333
|
T | C | 19 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(16): Show | 19 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.534-5620A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282333 | ||||||
| chr3:101282604
|
C | A | 1 | a0002c0002t0011g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.534-5891G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282604 | ||||||
| chr3:101282638
|
T | C | 5 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-5925A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282638 | ||||||
| chr3:101282748
|
T | C | 1 | a0002c0003t0024g0264 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.534-6035A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282748 | ||||||
| chr3:101282836
|
G | T | 1 | a0002c0003t0003g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.534-6123C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282836 | ||||||
| chr3:101282913
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-6200C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282913 | ||||||
| chr3:101282915
|
A | G | 58 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.534-6202T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282915 | ||||||
| chr3:101283018
|
T | G | 325 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.534-6305A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283018 | ||||||
| chr3:101283092
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-6379C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283092 | ||||||
| chr3:101283171
|
C | T | 1 | a0002c0002t0084g0086 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.534-6458G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283171 | ||||||
| chr3:101283179
|
T | G | 1 | a0002c0003t0002g0261 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.534-6466A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283179 | ||||||
| chr3:101283213
|
C | T | 8 | a0001c0001t0001g0072a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG02027.hp2 HG02071.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-6500G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283213 | ||||||
| chr3:101283317
|
T | C | 19 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(16): Show | 19 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.534-6604A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283317 | ||||||
| chr3:101283453
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.534-6740A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283453 | ||||||
| chr3:101283520
|
C | T | 3 | a0002c0002t0038g0342a0002c0002t0085g0341a0002c0002t0087g0340 | 3 | HG03486.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.534-6807G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283520 | ||||||
| chr3:101283699
|
C | T | 24 | a0002c0003t0002g0003a0002c0003t0002g0265a0002c0003t0002g0267others(21): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.534-6986G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283699 | ||||||
| chr3:101283895
|
TA | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.534-7183delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283895 | ||||||
| chr3:101284198
|
G | A | 1 | a0002c0002t0092g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.533+7281C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284198 | ||||||
| chr3:101284220
|
A | G | 1 | a0002c0003t0075g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.533+7259T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284220 | ||||||
| chr3:101284379
|
A | G | 1 | a0002c0003t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.533+7100T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284379 | ||||||
| chr3:101284565
|
C | CA | 232 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.533+6913dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284565 | ||||||
| chr3:101284565
|
C | CAA | 17 | a0001c0001t0001g0010a0001c0001t0001g0135a0001c0001t0001g0137others(14): Show | 18 | HG01884.hp2 HG01975.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.533+6912_533+6913d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284565 | ||||||
| chr3:101284771
|
T | C | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.533+6708A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284771 | ||||||
| chr3:101285065
|
A | G | 1 | a0001c0001t0043g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.533+6414T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285065 | ||||||
| chr3:101285336
|
G | A | 58 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.533+6143C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285336 | ||||||
| chr3:101285491
|
C | A | 1 | a0002c0003t0002g0299 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.533+5988G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285491 | ||||||
| chr3:101285524
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533+5955T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285524 | ||||||
| chr3:101285538
|
T | C | 4 | a0001c0001t0007g0001a0001c0001t0007g0054a0001c0001t0007g0055others(1): Show | 6 | NA18946.hp2 NA18947.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.533+5941A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285538 | ||||||
| chr3:101285575
|
G | A | 1 | a0001c0001t0007g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.533+5904C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285575 | ||||||
| chr3:101285628
|
T | C | 15 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(12): Show | 15 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.533+5851A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285628 | ||||||
| chr3:101285711
|
G | C | 5 | a0001c0001t0007g0037a0001c0001t0007g0038a0001c0001t0022g0056others(2): Show | 5 | HG00621.hp1 NA18948.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+5768C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285711 | ||||||
| chr3:101285828
|
T | G | 2 | a0001c0001t0001g0254a0002c0002t0086g0094 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.533+5651A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285828 | ||||||
| chr3:101285964
|
C | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.533+5515G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285964 | ||||||
| chr3:101285975
|
A | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+5504T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285975 | ||||||
| chr3:101286091
|
TCCTTCTC others(4): Show |
T | 1 | a0001c0001t0001g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.533+5377_533+5387d others(13): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286091 | ||||||
| chr3:101286263
|
A | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0182others(2): Show | 5 | HG01074.hp1 HG01978.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+5216T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286263 | ||||||
| chr3:101286346
|
A | G | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+5133T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286346 | ||||||
| chr3:101286394
|
C | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+5085G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286394 | ||||||
| chr3:101286424
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+5055A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286424 | ||||||
| chr3:101286516
|
T | C | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.533+4963A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286516 | ||||||
| chr3:101286659
|
G | A | 1 | a0001c0001t0043g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.533+4820C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286659 | ||||||
| chr3:101286703
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+4776G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286703 | ||||||
| chr3:101286937
|
C | T | 1 | a0002c0003t0019g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.533+4542G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286937 | ||||||
| chr3:101287277
|
G | T | 1 | a0001c0001t0025g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533+4202C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287277 | ||||||
| chr3:101287281
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.533+4198C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287281 | ||||||
| chr3:101287309
|
T | C | 1 | a0002c0002t0017g0213 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.533+4170A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287309 | ||||||
| chr3:101287360
|
T | G | 1 | a0003c0004t0048g0345 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.533+4119A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287360 | ||||||
| chr3:101287655
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+3824T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287655 | ||||||
| chr3:101287725
|
T | C | 1 | a0001c0001t0025g0058 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.533+3754A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287725 | ||||||
| chr3:101287740
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533+3739A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287740 | ||||||
| chr3:101287793
|
A | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+3686T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287793 | ||||||
| chr3:101288034
|
C | T | 1 | a0001c0001t0021g0045 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.533+3445G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288034 | ||||||
| chr3:101288043
|
C | A | 1 | a0002c0002t0009g0214 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.533+3436G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288043 | ||||||
| chr3:101288315
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0170others(1): Show | 4 | HG01175.hp1 HG01256.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+3164C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288315 | ||||||
| chr3:101288400
|
T | A | 1 | a0001c0001t0055g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.533+3079A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288400 | ||||||
| chr3:101288705
|
C | T | 2 | a0001c0001t0036g0252a0001c0001t0071g0251 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.533+2774G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288705 | ||||||
| chr3:101288706
|
G | A | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533+2773C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288706 | ||||||
| chr3:101288976
|
T | A | 1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+2503A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288976 | ||||||
| chr3:101290027
|
C | T | 1 | a0001c0001t0013g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.533+1452G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290027 | ||||||
| chr3:101290034
|
G | A | 1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+1445C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290034 | ||||||
| chr3:101290064
|
A | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+1415T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290064 | ||||||
| chr3:101290065
|
T | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+1414A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290065 | ||||||
| chr3:101290127
|
G | T | 320 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.533+1352C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290127 | ||||||
| chr3:101290163
|
A | T | 3 | a0002c0002t0004g0196a0002c0002t0015g0186a0002c0002t0026g0197 | 3 | NA18947.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.533+1316T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290163 | ||||||
| chr3:101290221
|
G | A | 1 | a0001c0001t0010g0062 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.533+1258C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290221 | ||||||
| chr3:101290277
|
C | T | 1 | a0001c0001t0025g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533+1202G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290277 | ||||||
| chr3:101290278
|
G | A | 1 | a0002c0003t0002g0304 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.533+1201C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290278 | ||||||
| chr3:101290327
|
C | T | 1 | a0002c0003t0003g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.533+1152G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290327 | ||||||
| chr3:101290480
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.533+999C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290480 | ||||||
| chr3:101290487
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533+992G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290487 | ||||||
| chr3:101290783
|
T | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533+696A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290783 | ||||||
| chr3:101290878
|
C | T | 1 | a0002c0002t0001g0044 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.533+601G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290878 | ||||||
| chr3:101290915
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.533+564A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290915 | ||||||
| chr3:101290955
|
T | C | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.533+524A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290955 | ||||||
| chr3:101290963
|
T | A | 4 | a0001c0001t0066g0231a0001c0001t0069g0229a0001c0001t0072g0230others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+516A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290963 | ||||||
| chr3:101291023
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.533+456G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291023 | ||||||
| chr3:101291207
|
T | C | 1 | a0002c0003t0056g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.533+272A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291207 | ||||||
| chr3:101291281
|
G | A | 1 | a0001c0001t0022g0095 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.533+198C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291281 | ||||||
| chr3:101291299
|
T | C | 3 | a0002c0003t0002g0297a0002c0003t0003g0263a0002c0003t0057g0258 | 3 | NA18955.hp1 NA18969.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.533+180A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291299 | ||||||
| chr3:101291370
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0136others(1): Show | 5 | HG02738.hp2 HG03704.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+109C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291370 | ||||||
| chr3:101291413
|
G | A | 1 | a0001c0001t0010g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.533+66C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291413 | ||||||
| chr3:101291655
|
G | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-145C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101291655 | ||||||
| chr3:101291834
|
C | A | 1 | a0001c0001t0022g0059 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.502-324G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101291834 | ||||||
| chr3:101291988
|
G | A | 1 | a0001c0001t0043g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502-478C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101291988 | ||||||
| chr3:101292001
|
C | A | 1 | a0003c0009t0049g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.502-491G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292001 | ||||||
| chr3:101292019
|
C | T | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-509G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292019 | ||||||
| chr3:101292022
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-512G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292022 | ||||||
| chr3:101292166
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 73 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.502-656A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292166 | ||||||
| chr3:101292279
|
G | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0112others(6): Show | 11 | NA18747.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-769C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292279 | ||||||
| chr3:101292339
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-829G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292339 | ||||||
| chr3:101292585
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0135a0001c0001t0001g0146others(3): Show | 7 | NA18939.hp1 NA18941.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-1075T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292585 | ||||||
| chr3:101292658
|
C | T | 1 | a0001c0001t0054g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.502-1148G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292658 | ||||||
| chr3:101292660
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-1150G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292660 | ||||||
| chr3:101292661
|
C | G | 1 | a0001c0001t0051g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.502-1151G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292661 | ||||||
| chr3:101292693
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 93 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.502-1183G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292693 | ||||||
| chr3:101292780
|
T | C | 1 | a0002c0003t0003g0298 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.502-1270A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292780 | ||||||
| chr3:101292841
|
A | C | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502-1331T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292841 | ||||||
| chr3:101292842
|
T | C | 1 | a0002c0003t0002g0304 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.502-1332A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292842 | ||||||
| chr3:101292896
|
A | C | 8 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0140others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-1386T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292896 | ||||||
| chr3:101292973
|
G | A | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-1463C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292973 | ||||||
| chr3:101293067
|
G | A | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.502-1557C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293067 | ||||||
| chr3:101293262
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-1752G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293262 | ||||||
| chr3:101293490
|
A | G | 2 | a0001c0001t0012g0085a0001c0001t0014g0105 | 2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.502-1980T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293490 | ||||||
| chr3:101293506
|
TA | T | 4 | a0002c0002t0011g0004a0002c0002t0011g0322a0002c0002t0015g0324others(1): Show | 6 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-1997delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293506 | ||||||
| chr3:101293535
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-2025G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293535 | ||||||
| chr3:101293542
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-2032T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293542 | ||||||
| chr3:101293623
|
C | T | 2 | a0002c0002t0009g0316a0002c0002t0026g0323 | 2 | HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.502-2113G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293623 | ||||||
| chr3:101293692
|
A | G | 1 | a0002c0002t0004g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.502-2182T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293692 | ||||||
| chr3:101293823
|
A | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-2313T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293823 | ||||||
| chr3:101293979
|
G | A | 1 | a0001c0001t0082g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.502-2469C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293979 | ||||||
| chr3:101293987
|
A | T | 1 | a0002c0003t0002g0003 | 3 | NA18979.hp1 NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.502-2477T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293987 | ||||||
| chr3:101294037
|
A | G | 1 | a0001c0001t0012g0074 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.502-2527T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294037 | ||||||
| chr3:101294138
|
G | A | 1 | a0002c0002t0042g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.502-2628C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294138 | ||||||
| chr3:101294156
|
T | C | 3 | a0001c0001t0012g0110a0001c0001t0070g0109a0001c0001t0078g0111 | 3 | HG01952.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.502-2646A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294156 | ||||||
| chr3:101294610
|
T | C | 1 | a0001c0001t0055g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.502-3100A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294610 | ||||||
| chr3:101294754
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.502-3244T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294754 | ||||||
| chr3:101294854
|
CT | C | 6 | a0001c0001t0020g0060a0002c0002t0009g0217a0002c0002t0015g0102others(3): Show | 6 | NA18747.hp1 NA18945.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-3345delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294854 | ||||||
| chr3:101294863
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.502-3353T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294863 | ||||||
| chr3:101294935
|
G | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-3425C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294935 | ||||||
| chr3:101294956
|
G | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-3446C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294956 | ||||||
| chr3:101295137
|
G | T | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502-3627C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295137 | ||||||
| chr3:101295178
|
G | C | 1 | a0012c0010t0017g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.502-3668C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295178 | ||||||
| chr3:101295271
|
G | A | 1 | a0001c0001t0077g0043 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.502-3761C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295271 | ||||||
| chr3:101295460
|
G | A | 1 | a0001c0001t0065g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.502-3950C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295460 | ||||||
| chr3:101295528
|
T | C | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.502-4018A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295528 | ||||||
| chr3:101295659
|
AT | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0131others(5): Show | 9 | HG02559.hp2 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.502-4150delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295659 | ||||||
| chr3:101295738
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.502-4228T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295738 | ||||||
| chr3:101295965
|
A | G | 5 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4455T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295965 | ||||||
| chr3:101296110
|
G | T | 321 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.502-4600C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296110 | ||||||
| chr3:101296169
|
G | A | 1 | a0001c0001t0010g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502-4659C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296169 | ||||||
| chr3:101296261
|
T | A | 1 | a0002c0003t0005g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.502-4751A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296261 | ||||||
| chr3:101296268
|
C | A | 5 | a0002c0003t0018g0219a0002c0003t0018g0220a0002c0003t0018g0221others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4758G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296268 | ||||||
| chr3:101296698
|
A | AT | 241 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.502-5189dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296698 | ||||||
| chr3:101296709
|
G | T | 1 | a0002c0002t0004g0196 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.502-5199C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296709 | ||||||
| chr3:101296711
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-5201A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296711 | ||||||
| chr3:101297048
|
G | A | 1 | a0002c0003t0002g0299 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.502-5538C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297048 | ||||||
| chr3:101297053
|
G | C | 58 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.502-5543C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297053 | ||||||
| chr3:101297054
|
C | T | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-5544G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297054 | ||||||
| chr3:101297119
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.502-5609C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297119 | ||||||
| chr3:101297151
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-5641C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297151 | ||||||
| chr3:101297296
|
A | G | 1 | a0002c0002t0040g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502-5786T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297296 | ||||||
| chr3:101297453
|
G | C | 3 | a0001c0001t0036g0252a0001c0001t0071g0251a0001c0001t0074g0250 | 3 | HG02055.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.502-5943C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297453 | ||||||
| chr3:101297546
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-6036T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297546 | ||||||
| chr3:101297585
|
T | G | 1 | a0002c0002t0090g0339 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.502-6075A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297585 | ||||||
| chr3:101297724
|
A | G | 59 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(56): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.502-6214T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297724 | ||||||
| chr3:101297990
|
C | G | 1 | a0002c0002t0026g0235 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.501+6156G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297990 | ||||||
| chr3:101298059
|
T | G | 1 | a0001c0001t0008g0033 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.501+6087A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298059 | ||||||
| chr3:101298080
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+6066A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298080 | ||||||
| chr3:101298229
|
T | C | 1 | a0001c0001t0012g0041 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.501+5917A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298229 | ||||||
| chr3:101298320
|
A | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0182others(2): Show | 5 | HG01074.hp1 HG01978.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+5826T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298320 | ||||||
| chr3:101298356
|
CCTGT | C | 4 | a0001c0001t0066g0231a0001c0001t0069g0229a0001c0001t0072g0230others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+5786_501+5789d others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298356 | ||||||
| chr3:101298385
|
A | G | 4 | a0001c0001t0012g0110a0001c0001t0070g0109a0001c0001t0073g0108others(1): Show | 4 | HG01952.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+5761T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298385 | ||||||
| chr3:101298409
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+5737T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298409 | ||||||
| chr3:101298774
|
T | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.501+5372A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298774 | ||||||
| chr3:101298803
|
C | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+5343G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298803 | ||||||
| chr3:101298939
|
T | C | 3 | a0001c0001t0035g0025a0001c0001t0035g0026a0008c0015t0076g0027 | 3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.501+5207A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298939 | ||||||
| chr3:101299389
|
C | T | 1 | a0001c0001t0023g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.501+4757G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299389 | ||||||
| chr3:101299486
|
G | A | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+4660C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299486 | ||||||
| chr3:101299542
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+4604T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299542 | ||||||
| chr3:101299570
|
A | G | 322 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.501+4576T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299570 | ||||||
| chr3:101299584
|
A | AT | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.501+4561dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299584 | ||||||
| chr3:101299620
|
G | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.501+4526C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299620 | ||||||
| chr3:101299643
|
G | A | 2 | a0001c0001t0010g0062a0001c0001t0016g0061 | 2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.501+4503C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299643 | ||||||
| chr3:101300142
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.501+4004C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300142 | ||||||
| chr3:101300143
|
G | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.501+4003C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300143 | ||||||
| chr3:101300307
|
C | G | 1 | a0001c0001t0035g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.501+3839G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300307 | ||||||
| chr3:101300408
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.501+3738G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300408 | ||||||
| chr3:101300418
|
G | A | 1 | a0013c0018t0005g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.501+3728C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300418 | ||||||
| chr3:101300423
|
C | T | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.501+3723G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300423 | ||||||
| chr3:101300550
|
T | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.501+3596A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300550 | ||||||
| chr3:101300564
|
T | C | 1 | a0014c0019t0021g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.501+3582A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300564 | ||||||
| chr3:101300567
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.501+3579G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300567 | ||||||
| chr3:101300752
|
T | G | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.501+3394A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300752 | ||||||
| chr3:101300924
|
A | T | 13 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+3222T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300924 | ||||||
| chr3:101301002
|
T | C | 1 | a0001c0001t0014g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.501+3144A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301002 | ||||||
| chr3:101301003
|
C | T | 1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.501+3143G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301003 | ||||||
| chr3:101301196
|
T | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.501+2950A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301196 | ||||||
| chr3:101301376
|
C | A | 1 | a0002c0002t0093g0224 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.501+2770G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301376 | ||||||
| chr3:101301623
|
T | C | 1 | a0002c0002t0094g0225 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501+2523A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301623 | ||||||
| chr3:101301649
|
C | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.501+2497G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301649 | ||||||
| chr3:101301916
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+2230A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301916 | ||||||
| chr3:101302033
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.501+2113T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302033 | ||||||
| chr3:101302193
|
T | C | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+1953A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302193 | ||||||
| chr3:101302229
|
A | T | 1 | a0001c0001t0001g0011 | 2 | NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.501+1917T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302229 | ||||||
| chr3:101302311
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.501+1835T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302311 | ||||||
| chr3:101302346
|
G | T | 1 | a0001c0001t0010g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.501+1800C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302346 | ||||||
| chr3:101302746
|
T | C | 1 | a0002c0002t0004g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.501+1400A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302746 | ||||||
| chr3:101302755
|
G | A | 95 | a0001c0001t0001g0090a0001c0001t0006g0014a0001c0001t0006g0015others(92): Show | 99 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.501+1391C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302755 | ||||||
| chr3:101302803
|
A | G | 59 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(56): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.501+1343T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302803 | ||||||
| chr3:101302882
|
C | T | 3 | a0001c0001t0032g0081a0001c0001t0032g0099a0001c0001t0064g0064 | 3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.501+1264G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302882 | ||||||
| chr3:101302926
|
G | A | 5 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+1220C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302926 | ||||||
| chr3:101303021
|
A | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.501+1125T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303021 | ||||||
| chr3:101303134
|
G | C | 41 | a0001c0001t0001g0090a0001c0001t0006g0014a0001c0001t0006g0015others(38): Show | 42 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.501+1012C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303134 | ||||||
| chr3:101303164
|
T | A | 4 | a0001c0001t0012g0110a0001c0001t0070g0109a0001c0001t0073g0108others(1): Show | 4 | HG01952.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+982A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303164 | ||||||
| chr3:101303203
|
T | C | 1 | a0002c0002t0004g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.501+943A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303203 | ||||||
| chr3:101303346
|
T | C | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.501+800A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303346 | ||||||
| chr3:101303397
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.501+749C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303397 | ||||||
| chr3:101303408
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.501+738C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303408 | ||||||
| chr3:101303536
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0131others(5): Show | 9 | HG02559.hp2 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.501+610G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303536 | ||||||
| chr3:101303546
|
G | A | 1 | a0002c0002t0038g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.501+600C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303546 | ||||||
| chr3:101303828
|
T | G | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.501+318A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303828 | ||||||
| chr3:101303835
|
C | A | 1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.501+311G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303835 | ||||||
| chr3:101303972
|
G | A | 5 | a0002c0002t0038g0342a0002c0002t0085g0341a0002c0002t0087g0340others(2): Show | 5 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+174C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303972 | ||||||
| chr3:101304032
|
T | C | 59 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(56): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.501+114A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101304032 | ||||||
| chr3:101304584
|
A | G | 3 | a0001c0001t0050g0245a0001c0001t0051g0244a0002c0003t0098g0243 | 3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.335-272T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304584 | ||||||
| chr3:101304627
|
T | C | 1 | a0001c0001t0023g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.335-315A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304627 | ||||||
| chr3:101304722
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.335-410G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304722 | ||||||
| chr3:101304739
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.335-427T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304739 | ||||||
| chr3:101304855
|
T | TA | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.335-544dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304855 | ||||||
| chr3:101304895
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.335-583G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304895 | ||||||
| chr3:101304904
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 101 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.335-592T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304904 | ||||||
| chr3:101305001
|
C | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-689G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305001 | ||||||
| chr3:101305037
|
C | T | 1 | a0001c0001t0058g0334 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.335-725G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305037 | ||||||
| chr3:101305273
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.335-961A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305273 | ||||||
| chr3:101305303
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.335-991T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305303 | ||||||
| chr3:101305373
|
G | A | 1 | a0002c0002t0038g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.335-1061C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305373 | ||||||
| chr3:101305407
|
T | C | 1 | a0001c0001t0065g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.335-1095A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305407 | ||||||
| chr3:101305436
|
A | G | 1 | a0013c0018t0005g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.335-1124T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305436 | ||||||
| chr3:101305502
|
C | T | 2 | a0003c0004t0047g0343a0003c0004t0048g0345 | 2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.335-1190G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305502 | ||||||
| chr3:101305677
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(258): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.335-1365T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305677 | ||||||
| chr3:101305680
|
A | T | 1 | a0002c0002t0011g0322 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.335-1368T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305680 | ||||||
| chr3:101305738
|
A | G | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-1426T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305738 | ||||||
| chr3:101305888
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-1576C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305888 | ||||||
| chr3:101305965
|
A | C | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.335-1653T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305965 | ||||||
| chr3:101306240
|
G | A | 3 | a0001c0001t0050g0245a0001c0001t0051g0244a0002c0003t0098g0243 | 3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.335-1928C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306240 | ||||||
| chr3:101306360
|
G | A | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-2048C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306360 | ||||||
| chr3:101306376
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.335-2064T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306376 | ||||||
| chr3:101306765
|
G | T | 1 | a0001c0001t0006g0014 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.335-2453C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306765 | ||||||
| chr3:101306821
|
G | C | 3 | a0001c0001t0066g0231a0001c0001t0069g0229a0001c0001t0072g0230 | 3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.335-2509C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306821 | ||||||
| chr3:101306876
|
A | G | 1 | a0002c0003t0075g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.335-2564T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306876 | ||||||
| chr3:101307093
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-2781A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307093 | ||||||
| chr3:101307095
|
C | G | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-2783G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307095 | ||||||
| chr3:101307110
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0172a0001c0001t0001g0174others(6): Show | 10 | HG01255.hp1 HG01358.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.335-2798C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307110 | ||||||
| chr3:101307466
|
C | T | 1 | a0002c0003t0024g0264 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.335-3154G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307466 | ||||||
| chr3:101307475
|
A | G | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-3163T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307475 | ||||||
| chr3:101307510
|
T | G | 3 | a0002c0002t0038g0342a0002c0002t0085g0341a0002c0002t0087g0340 | 3 | HG03486.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.335-3198A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307510 | ||||||
| chr3:101307757
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-3445A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307757 | ||||||
| chr3:101307913
|
C | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-3601G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307913 | ||||||
| chr3:101307928
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.335-3616G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307928 | ||||||
| chr3:101307955
|
C | A | 3 | a0002c0003t0002g0302a0002c0003t0002g0303a0002c0003t0002g0304 | 3 | HG01081.hp2 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.335-3643G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307955 | ||||||
| chr3:101308079
|
C | T | 9 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0033g0312others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-3767G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308079 | ||||||
| chr3:101308161
|
G | A | 2 | a0001c0001t0032g0081a0001c0001t0032g0099 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.335-3849C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308161 | ||||||
| chr3:101308244
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.335-3932A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308244 | ||||||
| chr3:101308249
|
C | T | 3 | a0001c0001t0033g0312a0001c0001t0033g0313a0001c0001t0068g0311 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.335-3937G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308249 | ||||||
| chr3:101308281
|
T | TG | 344 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(341): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.335-3970dupC | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308281 | ||||||
| chr3:101308449
|
G | C | 1 | a0001c0001t0010g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.335-4137C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308449 | ||||||
| chr3:101308664
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0134 | 2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.335-4352G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308664 | ||||||
| chr3:101308682
|
A | C | 1 | a0001c0001t0008g0033 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.335-4370T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308682 | ||||||
| chr3:101308710
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18939.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.335-4398A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308710 | ||||||
| chr3:101308751
|
C | T | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-4439G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308751 | ||||||
| chr3:101308915
|
T | C | 1 | a0003c0014t0044g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.335-4603A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308915 | ||||||
| chr3:101309073
|
G | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.335-4761C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309073 | ||||||
| chr3:101309277
|
T | G | 1 | a0002c0003t0024g0305 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.335-4965A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309277 | ||||||
| chr3:101309457
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-5145T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309457 | ||||||
| chr3:101309666
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.335-5354C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309666 | ||||||
| chr3:101309748
|
T | C | 1 | a0002c0002t0011g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.335-5436A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309748 | ||||||
| chr3:101309871
|
A | G | 1 | a0001c0001t0065g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.335-5559T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309871 | ||||||
| chr3:101309911
|
A | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0134 | 2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.335-5599T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309911 | ||||||
| chr3:101309999
|
G | A | 8 | a0001c0001t0036g0249a0001c0001t0036g0252a0001c0001t0071g0251others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-5687C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309999 | ||||||
| chr3:101310067
|
C | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-5755G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310067 | ||||||
| chr3:101310095
|
G | A | 321 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.335-5783C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310095 | ||||||
| chr3:101310305
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-5993A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310305 | ||||||
| chr3:101310377
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.335-6065G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310377 | ||||||
| chr3:101310393
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-6081G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310393 | ||||||
| chr3:101310415
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.335-6103G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310415 | ||||||
| chr3:101310429
|
C | T | 2 | a0001c0001t0032g0081a0001c0001t0032g0099 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.335-6117G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310429 | ||||||
| chr3:101310527
|
C | T | 321 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.335-6215G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310527 | ||||||
| chr3:101310559
|
C | CA | 11 | a0001c0001t0001g0247a0001c0001t0030g0335a0001c0001t0030g0336others(8): Show | 11 | HG01175.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.335-6248dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | ||||||
| chr3:101310559
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0016g0103a0001c0001t0059g0039 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.335-6262_335-6248d others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | ||||||
| chr3:101310559
|
CAAAAAAA others(9): Show |
C | 236 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.335-6263_335-6248d others(18): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | ||||||
| chr3:101310559
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0129 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.335-6264_335-6248d others(19): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | ||||||
| chr3:101310563
|
A | C | 58 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.335-6251T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310563 | ||||||
| chr3:101310577
|
AAAAAAAA others(6): Show |
A | 5 | a0002c0003t0002g0265a0002c0003t0002g0267a0002c0003t0003g0266others(2): Show | 5 | HG00673.hp1 HG02015.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.335-6278_335-6266d others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310577 | ||||||
| chr3:101310578
|
AAAAAAAA others(5): Show |
A | 52 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(49): Show | 54 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.335-6278_335-6267d others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310578 | ||||||
| chr3:101310579
|
AAAAAAAA others(4): Show |
A | 1 | a0002c0003t0002g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.335-6278_335-6268d others(13): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310579 | ||||||
| chr3:101310686
|
T | C | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-6374A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310686 | ||||||
| chr3:101310748
|
A | G | 3 | a0002c0003t0002g0261a0002c0003t0003g0259a0002c0003t0003g0260 | 3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.335-6436T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310748 | ||||||
| chr3:101310767
|
T | C | 1 | a0001c0001t0065g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.335-6455A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310767 | ||||||
| chr3:101310790
|
T | C | 1 | a0002c0002t0017g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.335-6478A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310790 | ||||||
| chr3:101310873
|
T | C | 1 | a0002c0003t0002g0306 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.335-6561A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310873 | ||||||
| chr3:101311179
|
T | TA | 246 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.335-6868dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311179 | ||||||
| chr3:101311566
|
G | A | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.335-7254C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311566 | ||||||
| chr3:101311714
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.335-7402T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311714 | ||||||
| chr3:101311807
|
T | G | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-7495A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311807 | ||||||
| chr3:101311956
|
C | T | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.334+7628G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311956 | ||||||
| chr3:101312025
|
C | CA | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 101 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.334+7558dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312025 | ||||||
| chr3:101312025
|
CA | C | 57 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(54): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.334+7558delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312025 | ||||||
| chr3:101312036
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.334+7548G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312036 | ||||||
| chr3:101312154
|
C | G | 2 | a0001c0001t0050g0245a0001c0001t0051g0244 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.334+7430G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312154 | ||||||
| chr3:101312333
|
A | T | 1 | a0002c0003t0003g0263 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.334+7251T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312333 | ||||||
| chr3:101312507
|
A | T | 1 | a0002c0003t0002g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.334+7077T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312507 | ||||||
| chr3:101312520
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.334+7064T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312520 | ||||||
| chr3:101312691
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.334+6893A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312691 | ||||||
| chr3:101312731
|
A | G | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.334+6853T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312731 | ||||||
| chr3:101312972
|
GGTCACAT others(10): Show |
G | 1 | a0001c0001t0014g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.334+6595_334+6611d others(19): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312972 | ||||||
| chr3:101313296
|
T | C | 1 | a0001c0001t0020g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.334+6288A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313296 | ||||||
| chr3:101313440
|
A | G | 58 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.334+6144T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313440 | ||||||
| chr3:101313607
|
C | T | 1 | a0001c0001t0061g0332 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.334+5977G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313607 | ||||||
| chr3:101313687
|
A | G | 1 | a0001c0001t0071g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+5897T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313687 | ||||||
| chr3:101313831
|
A | G | 1 | a0001c0001t0055g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.334+5753T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313831 | ||||||
| chr3:101313982
|
A | G | 1 | a0002c0002t0011g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.334+5602T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313982 | ||||||
| chr3:101314112
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+5472T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314112 | ||||||
| chr3:101314292
|
T | C | 2 | a0001c0001t0013g0024a0001c0001t0014g0023 | 2 | NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.334+5292A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314292 | ||||||
| chr3:101314433
|
C | T | 311 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.334+5151G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314433 | ||||||
| chr3:101314514
|
G | A | 1 | a0001c0001t0008g0006 | 2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.334+5070C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314514 | ||||||
| chr3:101314690
|
T | C | 1 | a0002c0003t0005g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.334+4894A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314690 | ||||||
| chr3:101314841
|
A | T | 1 | a0001c0001t0034g0020 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.334+4743T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314841 | ||||||
| chr3:101314989
|
G | A | 1 | a0001c0001t0012g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.334+4595C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314989 | ||||||
| chr3:101315250
|
T | C | 73 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0010g0256others(70): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.334+4334A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315250 | ||||||
| chr3:101315356
|
T | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.334+4228A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315356 | ||||||
| chr3:101315517
|
TA | T | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.334+4066delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315517 | ||||||
| chr3:101315551
|
C | T | 1 | a0001c0001t0081g0333 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.334+4033G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315551 | ||||||
| chr3:101315552
|
G | A | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.334+4032C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315552 | ||||||
| chr3:101315660
|
G | A | 1 | a0001c0001t0014g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.334+3924C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315660 | ||||||
| chr3:101315777
|
A | C | 1 | a0002c0002t0092g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334+3807T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315777 | ||||||
| chr3:101315784
|
A | G | 69 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0010g0256others(66): Show | 71 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.334+3800T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315784 | ||||||
| chr3:101315862
|
C | A | 1 | a0002c0003t0098g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.334+3722G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315862 | ||||||
| chr3:101315900
|
G | GGTAAA | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3683_334+3684i others(7): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315900 | ||||||
| chr3:101315903
|
A | AAGCT | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3680_334+3681i others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315903 | ||||||
| chr3:101315908
|
G | T | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3676C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315908 | ||||||
| chr3:101315911
|
A | ATTT | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3672_334+3673i others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315911 | ||||||
| chr3:101315912
|
C | T | 3 | a0002c0002t0004g0317a0002c0002t0015g0318a0002c0002t0103g0315 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3672G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315912 | ||||||
| chr3:101315958
|
G | A | 1 | a0002c0002t0088g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.334+3626C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315958 | ||||||
| chr3:101316214
|
A | G | 58 | a0001c0001t0010g0256a0002c0003t0002g0003a0002c0003t0002g0261others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.334+3370T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316214 | ||||||
| chr3:101316258
|
G | C | 5 | a0001c0001t0008g0078a0001c0001t0010g0019a0001c0001t0010g0079others(2): Show | 6 | HG01123.hp1 HG01943.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+3326C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316258 | ||||||
| chr3:101316302
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+3282G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316302 | ||||||
| chr3:101316455
|
A | T | 1 | a0003c0004t0046g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.334+3129T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316455 | ||||||
| chr3:101316566
|
T | C | 1 | a0001c0001t0063g0080 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.334+3018A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316566 | ||||||
| chr3:101316767
|
A | G | 2 | a0002c0003t0056g0253a0003c0009t0049g0255 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.334+2817T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316767 | ||||||
| chr3:101316866
|
T | C | 1 | a0002c0002t0004g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.334+2718A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316866 | ||||||
| chr3:101316946
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.334+2638C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316946 | ||||||
| chr3:101316972
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+2612C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316972 | ||||||
| chr3:101317095
|
GTGGGCAT others(6): Show |
G | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+2476_334+2488d others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317095 | ||||||
| chr3:101317173
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+2411T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317173 | ||||||
| chr3:101317185
|
G | A | 19 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0030g0335others(16): Show | 19 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.334+2399C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317185 | ||||||
| chr3:101317937
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+1647G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317937 | ||||||
| chr3:101318114
|
C | T | 3 | a0002c0003t0002g0261a0002c0003t0003g0259a0002c0003t0003g0260 | 3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.334+1470G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318114 | ||||||
| chr3:101318148
|
TAAATAAT others(4): Show |
T | 1 | a0002c0002t0009g0029 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.334+1425_334+1435d others(13): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318148 | ||||||
| chr3:101318149
|
A | AAAT | 55 | a0001c0001t0001g0072a0001c0001t0006g0014a0001c0001t0006g0050others(52): Show | 58 | HG00438.hp2 HG00621.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.334+1432_334+1434d others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
A | AAATAAT | 18 | a0001c0001t0007g0037a0001c0001t0007g0038a0001c0001t0008g0006others(15): Show | 19 | HG00642.hp1 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.334+1429_334+1434d others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
A | AAATAATA others(2): Show |
6 | a0001c0001t0013g0032a0001c0001t0021g0031a0001c0001t0036g0249others(3): Show | 6 | HG00280.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+1426_334+1434d others(11): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
A | AAATAATA others(5): Show |
1 | a0001c0001t0013g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.334+1423_334+1434d others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
AAAT | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0112others(20): Show | 25 | HG00597.hp1 HG00673.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.334+1432_334+1434d others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
AAATAAT | A | 12 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0010g0256others(9): Show | 12 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.334+1429_334+1434d others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
AAATAATA others(2): Show |
A | 124 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.334+1426_334+1434d others(11): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
AAATAATA others(5): Show |
A | 60 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.334+1423_334+1434d others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
AAATAATA others(8): Show |
A | 3 | a0001c0001t0001g0237a0001c0001t0050g0245a0001c0001t0051g0244 | 3 | HG02486.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.334+1420_334+1434d others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318149
|
AAATAATA others(11): Show |
A | 1 | a0002c0003t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334+1417_334+1434d others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | ||||||
| chr3:101318156
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.334+1428T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318156 | ||||||
| chr3:101318191
|
A | T | 1 | a0001c0001t0001g0028 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.334+1393T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318191 | ||||||
| chr3:101318217
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+1367G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318217 | ||||||
| chr3:101318245
|
C | T | 322 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.334+1339G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318245 | ||||||
| chr3:101318280
|
C | T | 3 | a0001c0001t0035g0025a0001c0001t0035g0026a0008c0015t0076g0027 | 3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.334+1304G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318280 | ||||||
| chr3:101318498
|
T | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.334+1086A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318498 | ||||||
| chr3:101318707
|
A | G | 5 | a0001c0001t0010g0022a0001c0001t0013g0024a0001c0001t0014g0023others(2): Show | 5 | NA18957.hp2 NA18973.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+877T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318707 | ||||||
| chr3:101318857
|
C | T | 2 | a0001c0001t0010g0019a0001c0001t0014g0005 | 3 | HG03490.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.334+727G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318857 | ||||||
| chr3:101318882
|
G | A | 3 | a0001c0001t0050g0245a0001c0001t0051g0244a0002c0003t0098g0243 | 3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.334+702C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318882 | ||||||
| chr3:101318923
|
T | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.334+661A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318923 | ||||||
| chr3:101319132
|
T | G | 6 | a0001c0001t0030g0335a0001c0001t0030g0336a0001c0001t0058g0334others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+452A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319132 | ||||||
| chr3:101319253
|
T | G | 5 | a0002c0002t0038g0342a0002c0002t0085g0341a0002c0002t0087g0340others(2): Show | 5 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+331A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319253 | ||||||
| chr3:101319314
|
A | T | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334+270T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319314 | ||||||
| chr3:101319453
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.334+131C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319453 | ||||||
| chr3:101319495
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.334+89C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319495 | ||||||
| chr3:101319969
|
A | G | 3 | a0001c0001t0050g0245a0001c0001t0051g0244a0002c0003t0098g0243 | 3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.86-137T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101319969 | ||||||
| chr3:101319995
|
TC | T | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(1): Show | 4 | HG01978.hp1 HG02148.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-164delG | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101319995 | ||||||
| chr3:101320020
|
T | C | 3 | a0003c0004t0045g0344a0003c0004t0047g0343a0003c0004t0048g0345 | 3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.86-188A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320020 | ||||||
| chr3:101320030
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.86-198C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320030 | ||||||
| chr3:101320178
|
AAGT | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.85+107_85+109delAC others(1): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320178 | ||||||
| chr3:101320263
|
A | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.85+25T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320263 |