Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2936 |
|---|---|
| ensemblid | ENSG00000104687.14 |
| hgncid | 4623 |
| symbol | GSR |
| name | glutathione-disulfide reductase |
| refseq_nuc | NM_000637.5 |
| refseq_prot | NP_000628.2 |
| ensembl_nuc | ENST00000221130.11 |
| ensembl_prot | ENSP00000221130.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 30678066 |
| end | 30727846 |
| strand | - |
| ver | v1.2 |
| region | chr8:30678066-30727846 |
| region5000 | chr8:30673066-30732846 |
| regionname0 | GSR_chr8_30678066_30727846 |
| regionname5000 | GSR_chr8_30673066_30732846 |
| 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 | 1/1 | 522 | 320 | 77 | 64 | 127 | 13 | 37 | 100 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002 | 0/0 | 522 | 18 | 10 | 0 | 5 | 0 | 3 | 4 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0003 | 0/0 | 522 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0004 | 0/0 | 522 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0005 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0006 | 0/0 | 522 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| 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 | 1/1 | 1569 | 306 | 65 | 64 | 126 | 12 | 37 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0002 | 0/0 | 1569 | 17 | 9 | 0 | 5 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0003 | 0/0 | 1569 | 7 | 7 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0004 | 0/0 | 1569 | 6 | 5 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0005 | 0/0 | 1569 | 4 | 2 | 2 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0006 | 0/0 | 1569 | 4 | 4 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0007 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0008 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0009 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| c0010 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| 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 | 0/0 | 1461 | 64 | 7 | 13 | 27 | 5 | 12 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0002 | 0/0 | 1464 | 52 | 3 | 18 | 26 | 1 | 4 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0003 | 0/1 | 1465 | 47 | 5 | 13 | 19 | 1 | 8 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0004 | 0/0 | 1462 | 37 | 4 | 9 | 19 | 1 | 4 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0005 | 0/0 | 1462 | 14 | 14 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0006 | 1/0 | 1466 | 12 | 5 | 0 | 2 | 2 | 2 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0007 | 0/0 | 1464 | 12 | 7 | 0 | 5 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0008 | 0/0 | 1462 | 10 | 4 | 0 | 4 | 0 | 2 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0009 | 0/0 | 1464 | 10 | 2 | 2 | 6 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0010 | 0/0 | 1462 | 7 | 2 | 1 | 3 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0011 | 0/0 | 1463 | 6 | 1 | 0 | 5 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0012 | 0/0 | 1461 | 6 | 5 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0013 | 0/0 | 1465 | 6 | 0 | 0 | 5 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0014 | 0/0 | 1462 | 6 | 6 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0015 | 0/0 | 1466 | 5 | 2 | 2 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0016 | 0/0 | 1464 | 4 | 0 | 1 | 0 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0017 | 0/0 | 1462 | 4 | 0 | 3 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0018 | 0/0 | 1466 | 3 | 2 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0019 | 0/0 | 1461 | 3 | 1 | 0 | 1 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0020 | 0/0 | 1466 | 3 | 3 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0021 | 0/0 | 1465 | 3 | 0 | 0 | 0 | 2 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0022 | 0/0 | 1465 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0023 | 0/0 | 1462 | 2 | 1 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0024 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0025 | 0/0 | 1469 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0026 | 0/0 | 1463 | 2 | 1 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0027 | 0/0 | 1461 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0028 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0029 | 0/0 | 1466 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0030 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0031 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0032 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0033 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0034 | 0/0 | 1463 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0035 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0036 | 0/0 | 1463 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0037 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0038 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0039 | 0/0 | 1466 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0040 | 0/0 | 1464 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0041 | 0/0 | 1465 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0042 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0043 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0044 | 0/0 | 1466 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0045 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0046 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0047 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0048 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0049 | 0/0 | 1466 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| t0050 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| 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 | 2 | 0 | 1 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| 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 | 1/1 | 1569 | 306 | 65 | 64 | 126 | 12 | 37 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0003 | 0/0 | 1569 | 7 | 7 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004 | 0/0 | 1569 | 6 | 5 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0009 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002 | 0/0 | 1569 | 17 | 9 | 0 | 5 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0010 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0003c0006 | 0/0 | 1569 | 4 | 4 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0004c0005 | 0/0 | 1569 | 4 | 2 | 2 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0005c0008 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0006c0007 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3029 | 52 | 2 | 13 | 24 | 4 | 9 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0002 | 0/0 | 3032 | 52 | 3 | 18 | 26 | 1 | 4 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0003 | 0/1 | 3033 | 45 | 4 | 13 | 18 | 1 | 8 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0004 | 0/0 | 3030 | 36 | 3 | 9 | 19 | 1 | 4 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0005 | 0/0 | 3030 | 12 | 12 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0006 | 1/0 | 3034 | 11 | 5 | 0 | 2 | 1 | 2 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0007 | 0/0 | 3032 | 12 | 7 | 0 | 5 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0008 | 0/0 | 3030 | 9 | 3 | 0 | 4 | 0 | 2 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0009 | 0/0 | 3032 | 8 | 1 | 2 | 5 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0010 | 0/0 | 3030 | 6 | 2 | 0 | 3 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0011 | 0/0 | 3031 | 5 | 1 | 0 | 4 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0012 | 0/0 | 3029 | 2 | 1 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0013 | 0/0 | 3033 | 6 | 0 | 0 | 5 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0014 | 0/0 | 3030 | 5 | 5 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0015 | 0/0 | 3034 | 3 | 0 | 2 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0016 | 0/0 | 3032 | 4 | 0 | 1 | 0 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0017 | 0/0 | 3030 | 4 | 0 | 3 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0018 | 0/0 | 3034 | 2 | 1 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0019 | 0/0 | 3029 | 2 | 0 | 0 | 1 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0020 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0021 | 0/0 | 3033 | 3 | 0 | 0 | 0 | 2 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0022 | 0/0 | 3033 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0023 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0024 | 0/0 | 3029 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0026 | 0/0 | 3031 | 2 | 1 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0027 | 0/0 | 3029 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0028 | 0/0 | 3032 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0029 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0030 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0031 | 0/0 | 3032 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0032 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0033 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0034 | 0/0 | 3031 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0035 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0036 | 0/0 | 3031 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0038 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0039 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0040 | 0/0 | 3032 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0041 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0046 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0047 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0048 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0001t0049 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0003t0005 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0003t0012 | 0/0 | 3029 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0003t0015 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0003t0025 | 0/0 | 3037 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0003t0042 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004t0003 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004t0005 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004t0006 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004t0012 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004t0014 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0004t0045 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0001c0009t0001 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0001 | 0/0 | 3029 | 10 | 5 | 0 | 2 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0003 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0004 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0009 | 0/0 | 3032 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0011 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0019 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0020 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0002t0023 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0002c0010t0015 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0003c0006t0008 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0003c0006t0009 | 0/0 | 3032 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0003c0006t0012 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0003c0006t0018 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0004c0005t0010 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0004c0005t0043 | 0/0 | 3035 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0004c0005t0044 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0004c0005t0050 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0005c0008t0037 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| a0006c0007t0001 | 0/0 | 3029 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | copy fasta | chr8 | 30673066 | 30732846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0015g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0015g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0016g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0016g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0016g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0016g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0017g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0017g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0017g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0017g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0018g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0018g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0019g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0019g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0020g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0021g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0021g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0021g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0022g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0022g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0023g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0024g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0024g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0026g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0026g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0027g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0028g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0029g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0030g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0031g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0032g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0033g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0034g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0035g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0036g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0038g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0039g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0040g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0041g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0046g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0047g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0048g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0049g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0025g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0025g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0042g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0006g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0012g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0014g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0045g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0009t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0009g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0011g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0019g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0020g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0023g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0010t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0006t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0006t0009g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0006t0012g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0006t0018g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0005t0010g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0005t0043g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0005t0044g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0005t0050g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0005c0008t0037g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0006c0007t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0255 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0170 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00140 | hp2 | a0001 | c0001 | t0021 | g0305 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0106 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00323 | hp1 | a0001 | c0001 | t0021 | g0307 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00323 | hp2 | a0006 | c0007 | t0001 | g0173 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00438 | hp1 | a0001 | c0001 | t0035 | g0100 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00558 | hp1 | a0001 | c0001 | t0011 | g0180 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00597 | hp2 | a0001 | c0001 | t0015 | g0066 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00621 | hp2 | a0002 | c0002 | t0011 | g0341 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00733 | hp2 | a0001 | c0001 | t0016 | g0262 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00738 | hp2 | a0004 | c0005 | t0010 | g0005 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01069 | hp1 | a0001 | c0001 | t0027 | g0129 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01243 | hp1 | a0004 | c0005 | t0043 | g0003 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01243 | hp2 | a0001 | c0001 | t0017 | g0039 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01255 | hp1 | a0001 | c0001 | t0015 | g0172 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01255 | hp2 | a0001 | c0001 | t0026 | g0243 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0137 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0186 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0187 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01361 | hp1 | a0001 | c0001 | t0015 | g0154 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01516 | hp1 | a0001 | c0001 | t0019 | g0073 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0142 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01891 | hp1 | a0001 | c0003 | t0012 | g0012 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01891 | hp2 | a0002 | c0002 | t0020 | g0322 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01934 | hp2 | a0001 | c0001 | t0017 | g0033 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0294 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02004 | hp1 | a0001 | c0001 | t0023 | g0118 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02055 | hp1 | a0001 | c0001 | t0020 | g0168 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02055 | hp2 | a0001 | c0004 | t0005 | g0328 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02074 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02083 | hp2 | a0001 | c0001 | t0041 | g0160 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02145 | hp1 | a0001 | c0001 | t0033 | g0049 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02145 | hp2 | a0004 | c0005 | t0044 | g0004 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CDX | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | CDX | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0320 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0215 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0237 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0217 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02300 | hp2 | a0001 | c0001 | t0017 | g0038 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02451 | hp1 | a0003 | c0006 | t0012 | g0342 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0266 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0206 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0298 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02615 | hp2 | a0001 | c0001 | t0022 | g0211 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0269 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0235 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0041 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02683 | hp2 | a0001 | c0001 | t0013 | g0293 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02717 | hp1 | a0001 | c0001 | t0038 | g0214 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0236 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02723 | hp2 | a0001 | c0001 | t0014 | g0020 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02809 | hp1 | a0001 | c0004 | t0045 | g0330 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02886 | hp1 | a0001 | c0003 | t0025 | g0010 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02886 | hp2 | a0001 | c0003 | t0042 | g0007 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0337 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02896 | hp2 | a0001 | c0001 | t0024 | g0213 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02897 | hp1 | a0001 | c0001 | t0024 | g0212 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0021 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0326 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02965 | hp1 | a0001 | c0001 | t0047 | g0280 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02965 | hp2 | a0001 | c0004 | t0014 | g0319 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0339 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02970 | hp2 | a0004 | c0005 | t0050 | g0346 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0327 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0144 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03041 | hp2 | a0003 | c0006 | t0009 | g0343 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03098 | hp1 | a0001 | c0001 | t0048 | g0017 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0324 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0205 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03195 | hp1 | a0005 | c0008 | t0037 | g0204 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0216 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03225 | hp1 | a0002 | c0002 | t0019 | g0321 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03225 | hp2 | a0001 | c0003 | t0025 | g0009 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03239 | hp1 | a0001 | c0001 | t0016 | g0095 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03239 | hp2 | a0001 | c0001 | t0034 | g0159 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0018 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0248 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0031 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03516 | hp2 | a0001 | c0004 | t0012 | g0323 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0055 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0340 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0090 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0042 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0158 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03834 | hp2 | a0001 | c0001 | t0040 | g0309 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0331 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04115 | hp1 | a0001 | c0001 | t0016 | g0310 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04115 | hp2 | a0001 | c0001 | t0036 | g0197 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04199 | hp2 | a0001 | c0001 | t0021 | g0303 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0115 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0222 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18906 | hp1 | a0002 | c0002 | t0023 | g0338 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0265 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18941 | hp2 | a0001 | c0001 | t0009 | g0183 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18943 | hp2 | a0001 | c0001 | t0010 | g0152 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18948 | hp1 | a0001 | c0001 | t0028 | g0138 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18954 | hp2 | a0001 | c0001 | t0013 | g0274 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18961 | hp2 | a0001 | c0001 | t0017 | g0036 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18962 | hp2 | a0001 | c0001 | t0010 | g0145 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18970 | hp2 | a0001 | c0001 | t0013 | g0289 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18971 | hp2 | a0001 | c0001 | t0013 | g0234 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18973 | hp2 | a0001 | c0001 | t0013 | g0245 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18977 | hp2 | a0001 | c0001 | t0011 | g0195 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0147 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18991 | hp1 | a0001 | c0001 | t0018 | g0077 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0181 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18992 | hp2 | a0001 | c0001 | t0009 | g0110 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18999 | hp1 | a0001 | c0001 | t0010 | g0202 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19002 | hp1 | a0001 | c0001 | t0013 | g0273 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19030 | hp2 | a0001 | c0001 | t0026 | g0167 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19043 | hp1 | a0001 | c0001 | t0049 | g0034 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0169 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0191 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19062 | hp1 | a0001 | c0009 | t0001 | g0027 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19062 | hp2 | a0001 | c0001 | t0030 | g0179 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19064 | hp2 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19068 | hp2 | a0001 | c0001 | t0031 | g0141 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19072 | hp1 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19072 | hp2 | a0001 | c0001 | t0046 | g0028 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19079 | hp1 | a0002 | c0002 | t0009 | g0329 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0264 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19088 | hp1 | a0001 | c0001 | t0019 | g0111 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19088 | hp2 | a0001 | c0001 | t0011 | g0276 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0334 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19240 | hp1 | a0003 | c0006 | t0018 | g0344 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20129 | hp1 | a0001 | c0003 | t0012 | g0011 | AFR | ASW | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20805 | hp2 | a0001 | c0004 | t0006 | g0332 | EUR | TSI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20905 | hp1 | a0001 | c0001 | t0016 | g0308 | SAS | GIH | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02109 | hp1 | a0003 | c0006 | t0008 | g0345 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02109 | hp2 | a0001 | c0001 | t0039 | g0231 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02486 | hp1 | a0001 | c0003 | t0015 | g0006 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02486 | hp2 | a0001 | c0001 | t0029 | g0032 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0325 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA21309 | hp1 | a0002 | c0010 | t0015 | g0016 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0114 | REF | REF | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0044 | REF | REF | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30692985
|
A | G | 1 | a0005 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.866T>C | p.Val289Ala | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/13 | 877/3034 | 866/1569 | 289/522 | chr8 | 30692985 | ||
| chr8:30703138
|
C | T | 1 | a0006 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.595G>A | p.Ala199Thr | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/13 | 606/3034 | 595/1569 | 199/522 | chr8 | 30703138 | ||
| chr8:30708107
|
G | A | 1 | a0002 | 18 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
missense_variant | MODERATE | c.457C>T | p.Arg153Cys | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/13 | 468/3034 | 457/1569 | 153/522 | chr8 | 30708107 | ||
| chr8:30727793
|
T | C | 1 | a0003 | 4 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.43A>G | p.Ser15Gly | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 54/3034 | 43/1569 | 15/522 | chr8 | 30727793 | ||
| chr8:30727795
|
G | T | 1 | a0004 | 4 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(1): Show |
missense_variant | MODERATE | c.41C>A | p.Pro14Gln | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 52/3034 | 41/1569 | 14/522 | chr8 | 30727795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30696473
|
G | A | 1 | a0001c0009 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.702C>T | p.Ser234Ser | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/13 | 713/3034 | 702/1569 | 234/522 | chr8 | 30696473 | ||
| chr8:30727575
|
A | G | 4 | a0001c0003a0001c0004a0002c0002others(1): Show | 34 | HG00621.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
synonymous_variant | LOW | c.261T>C | p.Gly87Gly | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 272/3034 | 261/1569 | 87/522 | chr8 | 30727575 | ||
| chr8:30727647
|
G | A | 2 | a0001c0004a0002c0002 | 23 | HG00621.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
synonymous_variant | LOW | c.189C>T | p.Ala63Ala | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 200/3034 | 189/1569 | 63/522 | chr8 | 30727647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30678101
|
T | C | 2 | a0001c0001t0029a0001c0001t0032 | 2 | HG02486.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1419A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1419 | chr8 | 30678101 | |||||
| chr8:30678116
|
A | G | 2 | a0001c0001t0029a0001c0001t0032 | 2 | HG02486.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1404T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1404 | chr8 | 30678116 | |||||
| chr8:30678143
|
C | A | 15 | a0001c0001t0001a0001c0001t0015a0001c0001t0019others(12): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1377G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1377 | chr8 | 30678143 | |||||
| chr8:30678210
|
T | C | 1 | a0001c0001t0021 | 3 | HG00140.hp2 HG00323.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1310 | chr8 | 30678210 | |||||
| chr8:30678340
|
A | AAT | 3 | a0001c0003t0025a0001c0003t0042a0001c0004t0045 | 4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179dupAT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1179 | chr8 | 30678340 | |||||
| chr8:30678357
|
ATATT | A | 5 | a0001c0001t0010a0001c0001t0014a0001c0004t0014others(2): Show | 14 | HG00738.hp2 HG01516.hp2 HG02723.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1162delAATA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1159 | chr8 | 30678357 | |||||
| chr8:30678359
|
AT | A | 8 | a0001c0001t0003a0001c0001t0013a0001c0001t0021others(5): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1160delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1160 | chr8 | 30678359 | |||||
| chr8:30678359
|
ATT | A | 4 | a0001c0001t0016a0001c0001t0028a0001c0001t0031others(1): Show | 7 | HG00733.hp2 HG03239.hp1 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1160delAA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1159 | chr8 | 30678359 | |||||
| chr8:30678359
|
ATTT | A | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 83 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1158_*1160delAAA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1158 | chr8 | 30678359 | |||||
| chr8:30678359
|
ATTTT | A | 18 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(15): Show | 76 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1157_*1160delAAAA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1157 | chr8 | 30678359 | |||||
| chr8:30678359
|
ATTTTT | A | 13 | a0001c0001t0001a0001c0001t0012a0001c0001t0019others(10): Show | 77 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1156_*1160delAAAA others(1): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1156 | chr8 | 30678359 | |||||
| chr8:30678361
|
T | A | 6 | a0001c0001t0020a0001c0001t0039a0001c0003t0025others(3): Show | 8 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1159A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1159 | chr8 | 30678361 | |||||
| chr8:30678362
|
T | A | 3 | a0001c0001t0013a0001c0001t0022a0004c0005t0044 | 9 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1158A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1158 | chr8 | 30678362 | |||||
| chr8:30678363
|
T | A | 5 | a0001c0001t0028a0001c0001t0031a0001c0001t0040others(2): Show | 5 | HG02809.hp1 HG02886.hp2 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1157A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1157 | chr8 | 30678363 | |||||
| chr8:30678364
|
T | A | 7 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(4): Show | 73 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1156A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1156 | chr8 | 30678364 | |||||
| chr8:30678365
|
T | A | 13 | a0001c0001t0005a0001c0001t0008a0001c0001t0023others(10): Show | 32 | HG00438.hp1 HG02004.hp1 HG02055.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1155A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1155 | chr8 | 30678365 | |||||
| chr8:30678366
|
T | A | 4 | a0001c0001t0007a0001c0001t0019a0001c0001t0036others(1): Show | 16 | HG01516.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1154A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1154 | chr8 | 30678366 | |||||
| chr8:30678367
|
T | A | 5 | a0001c0001t0005a0001c0001t0047a0001c0003t0005others(2): Show | 16 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1153 | chr8 | 30678367 | |||||
| chr8:30678369
|
T | A | 1 | a0005c0008t0037 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1151A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1151 | chr8 | 30678369 | |||||
| chr8:30678518
|
A | T | 1 | a0001c0001t0028 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1002T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1002 | chr8 | 30678518 | |||||
| chr8:30678555
|
T | G | 3 | a0001c0001t0014a0001c0001t0048a0001c0004t0014 | 7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 965 | chr8 | 30678555 | |||||
| chr8:30678613
|
C | T | 2 | a0001c0001t0020a0002c0002t0020 | 3 | HG01891.hp2 HG02055.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*907G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 907 | chr8 | 30678613 | |||||
| chr8:30678711
|
G | A | 1 | a0001c0001t0041 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*809C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 809 | chr8 | 30678711 | |||||
| chr8:30678952
|
C | G | 1 | a0001c0001t0027 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 568 | chr8 | 30678952 | |||||
| chr8:30678978
|
C | G | 1 | a0001c0003t0042 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 542 | chr8 | 30678978 | |||||
| chr8:30679011
|
T | C | 2 | a0001c0001t0024a0001c0001t0038 | 3 | HG02717.hp1 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 509 | chr8 | 30679011 | |||||
| chr8:30679064
|
A | G | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(55): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*456T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 456 | chr8 | 30679064 | |||||
| chr8:30679149
|
C | CA | 13 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(10): Show | 84 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*370dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 370 | chr8 | 30679149 | |||||
| chr8:30679276
|
T | G | 3 | a0001c0001t0014a0001c0001t0048a0001c0004t0014 | 7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 244 | chr8 | 30679276 | |||||
| chr8:30679370
|
G | C | 1 | a0001c0001t0049 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 150 | chr8 | 30679370 | |||||
| chr8:30727837
|
C | A | 1 | a0004c0005t0050 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 2 | chr8 | 30727837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30679706
|
CT | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(238): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1420-38delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679706 | ||||||
| chr8:30679710
|
T | C | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1420-41A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679710 | ||||||
| chr8:30679727
|
C | T | 1 | a0001c0001t0022g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1420-58G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679727 | ||||||
| chr8:30679780
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1420-111C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679780 | ||||||
| chr8:30679798
|
C | T | 2 | a0003c0006t0009g0343a0003c0006t0018g0344 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1420-129G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679798 | ||||||
| chr8:30679815
|
C | A | 71 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(68): Show | 71 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1420-146G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679815 | ||||||
| chr8:30679831
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1420-162C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679831 | ||||||
| chr8:30679852
|
C | T | 1 | a0001c0001t0035g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1420-183G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679852 | ||||||
| chr8:30680033
|
A | T | 1 | a0001c0001t0002g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1420-364T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680033 | ||||||
| chr8:30680381
|
G | GT | 21 | a0001c0001t0002g0188a0001c0001t0002g0224a0001c0001t0003g0114others(18): Show | 21 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1419+522dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680381 | ||||||
| chr8:30680381
|
G | GTT | 6 | a0001c0001t0003g0306a0001c0001t0003g0313a0001c0001t0007g0220others(3): Show | 6 | HG02486.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419+521_1419+522d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680381 | ||||||
| chr8:30680384
|
T | TTG | 33 | a0001c0001t0001g0064a0001c0001t0001g0098a0001c0001t0001g0109others(30): Show | 33 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1419+519_1419+520i others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680384 | ||||||
| chr8:30680385
|
T | TG | 207 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1419+518_1419+519i others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680385 | ||||||
| chr8:30680386
|
T | G | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1419+518A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680386 | ||||||
| chr8:30680392
|
T | G | 2 | a0001c0001t0004g0078a0001c0001t0018g0077 | 2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1419+512A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680392 | ||||||
| chr8:30680397
|
T | G | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1419+507A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680397 | ||||||
| chr8:30680447
|
G | T | 340 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(337): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1419+457C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680447 | ||||||
| chr8:30680481
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(77): Show | 81 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1419+423C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680481 | ||||||
| chr8:30680537
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(266): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1419+367T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680537 | ||||||
| chr8:30680548
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(249): Show | 253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1419+356A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680548 | ||||||
| chr8:30680560
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1419+344T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680560 | ||||||
| chr8:30680582
|
A | T | 2 | a0002c0002t0001g0335a0002c0002t0001g0336 | 2 | NA18960.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1419+322T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680582 | ||||||
| chr8:30681199
|
T | C | 2 | a0001c0001t0029g0032a0001c0001t0032g0031 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1286-162A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681199 | ||||||
| chr8:30681388
|
G | A | 1 | a0002c0010t0015g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1286-351C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681388 | ||||||
| chr8:30681448
|
C | T | 2 | a0001c0001t0004g0232a0001c0001t0004g0314 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1286-411G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681448 | ||||||
| chr8:30681480
|
G | A | 1 | a0002c0002t0004g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1286-443C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681480 | ||||||
| chr8:30681541
|
A | G | 1 | a0002c0002t0004g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1285+389T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681541 | ||||||
| chr8:30681597
|
G | A | 1 | a0001c0001t0002g0316 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1285+333C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681597 | ||||||
| chr8:30681621
|
A | G | 1 | a0001c0001t0049g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1285+309T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681621 | ||||||
| chr8:30681626
|
A | C | 3 | a0001c0001t0003g0250a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1285+304T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681626 | ||||||
| chr8:30681648
|
T | A | 1 | a0001c0001t0004g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1285+282A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681648 | ||||||
| chr8:30681752
|
C | T | 1 | a0001c0001t0005g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1285+178G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681752 | ||||||
| chr8:30681764
|
A | G | 2 | a0004c0005t0010g0005a0004c0005t0050g0346 | 2 | HG00738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1285+166T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681764 | ||||||
| chr8:30682106
|
T | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1154-45A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682106 | ||||||
| chr8:30682402
|
C | G | 2 | a0001c0001t0018g0215a0001c0001t0049g0034 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1154-341G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682402 | ||||||
| chr8:30682454
|
A | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(266): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1154-393T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682454 | ||||||
| chr8:30682561
|
A | C | 1 | a0001c0001t0007g0225 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1154-500T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682561 | ||||||
| chr8:30682658
|
C | T | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154-597G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682658 | ||||||
| chr8:30682770
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1154-709T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682770 | ||||||
| chr8:30682791
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(175): Show | 179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1154-730G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682791 | ||||||
| chr8:30682792
|
G | A | 70 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1154-731C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682792 | ||||||
| chr8:30682837
|
T | A | 4 | a0001c0001t0004g0080a0001c0001t0004g0081a0001c0001t0004g0178others(1): Show | 4 | HG01952.hp2 HG02486.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-776A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682837 | ||||||
| chr8:30682958
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1154-897C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682958 | ||||||
| chr8:30682959
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1154-898G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682959 | ||||||
| chr8:30682972
|
C | T | 1 | a0001c0001t0010g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1154-911G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682972 | ||||||
| chr8:30683181
|
C | A | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153+907G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683181 | ||||||
| chr8:30683440
|
T | C | 1 | a0001c0001t0020g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1153+648A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683440 | ||||||
| chr8:30683589
|
G | A | 2 | a0001c0001t0018g0215a0001c0001t0049g0034 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1153+499C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683589 | ||||||
| chr8:30683691
|
G | A | 1 | a0001c0001t0038g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153+397C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683691 | ||||||
| chr8:30683692
|
T | G | 3 | a0001c0001t0005g0207a0001c0001t0011g0206a0005c0008t0037g0204 | 3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1153+396A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683692 | ||||||
| chr8:30683754
|
C | CA | 79 | a0001c0001t0001g0153a0001c0001t0002g0047a0001c0001t0002g0050others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1153+333dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683754 | ||||||
| chr8:30683754
|
C | CAA | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 190 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1153+332_1153+333d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683754 | ||||||
| chr8:30684398
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1042-199G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684398 | ||||||
| chr8:30684414
|
A | G | 4 | a0001c0003t0025g0009a0001c0003t0025g0010a0001c0003t0042g0007others(1): Show | 4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-215T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684414 | ||||||
| chr8:30684418
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(78): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1042-219C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684418 | ||||||
| chr8:30684607
|
G | T | 1 | a0001c0001t0008g0041 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1042-408C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684607 | ||||||
| chr8:30684747
|
T | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0157 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1042-548A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684747 | ||||||
| chr8:30684809
|
G | A | 4 | a0001c0001t0012g0216a0001c0003t0012g0011a0001c0004t0012g0323others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-610C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684809 | ||||||
| chr8:30684926
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1042-727A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684926 | ||||||
| chr8:30684928
|
CATTT | C | 61 | a0001c0001t0001g0045a0001c0001t0002g0047a0001c0001t0002g0050others(58): Show | 61 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1042-733_1042-730d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684928
|
CATTTATT others(1): Show |
C | 85 | a0001c0001t0002g0061a0001c0001t0002g0070a0001c0001t0002g0102others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.1042-737_1042-730d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684928
|
CATTTATT others(5): Show |
C | 76 | a0001c0001t0001g0091a0001c0001t0001g0105a0001c0001t0001g0119others(73): Show | 77 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1042-741_1042-730d others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684928
|
CATTTATT others(9): Show |
C | 74 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(71): Show | 75 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1042-745_1042-730d others(18): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684928
|
CATTTATT others(13): Show |
C | 9 | a0001c0001t0004g0170a0001c0001t0013g0245a0001c0001t0013g0273others(6): Show | 9 | HG00099.hp2 HG00738.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042-749_1042-730d others(22): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684928
|
CATTTATT others(17): Show |
C | 10 | a0001c0001t0001g0096a0001c0001t0001g0153a0001c0001t0001g0176others(7): Show | 10 | HG02004.hp2 HG02257.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-753_1042-730d others(26): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684928
|
CATTTATT others(21): Show |
C | 11 | a0001c0001t0002g0224a0001c0001t0007g0209a0001c0001t0007g0217others(8): Show | 11 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1042-757_1042-730d others(30): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | ||||||
| chr8:30684954
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1042-755A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684954 | ||||||
| chr8:30684975
|
T | G | 2 | a0001c0001t0018g0215a0001c0001t0049g0034 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1042-776A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684975 | ||||||
| chr8:30685111
|
C | T | 86 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0025others(83): Show | 86 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1042-912G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685111 | ||||||
| chr8:30685146
|
G | A | 32 | a0001c0001t0003g0210a0001c0001t0003g0227a0001c0001t0003g0238others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.1042-947C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685146 | ||||||
| chr8:30685211
|
C | T | 1 | a0002c0002t0001g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1042-1012G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685211 | ||||||
| chr8:30685246
|
C | T | 1 | a0001c0001t0013g0289 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1042-1047G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685246 | ||||||
| chr8:30685252
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0165 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1042-1053C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685252 | ||||||
| chr8:30685379
|
C | A | 8 | a0001c0001t0004g0030a0001c0001t0004g0232a0001c0001t0004g0314others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1042-1180G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685379 | ||||||
| chr8:30685558
|
T | C | 1 | a0001c0003t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-1359A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685558 | ||||||
| chr8:30685734
|
G | A | 2 | a0004c0005t0010g0005a0004c0005t0050g0346 | 2 | HG00738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1042-1535C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685734 | ||||||
| chr8:30685751
|
G | A | 1 | a0002c0002t0004g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1042-1552C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685751 | ||||||
| chr8:30685901
|
C | T | 2 | a0001c0001t0009g0110a0001c0001t0030g0179 | 2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1042-1702G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685901 | ||||||
| chr8:30685913
|
G | A | 1 | a0001c0001t0018g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1042-1714C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685913 | ||||||
| chr8:30685985
|
C | CA | 14 | a0001c0001t0002g0190a0001c0001t0003g0114a0001c0001t0003g0218others(11): Show | 14 | HG01952.hp2 HG02155.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.1042-1787dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
C | CAA | 10 | a0001c0001t0002g0224a0001c0001t0007g0209a0001c0001t0007g0217others(7): Show | 10 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-1788_1042-178 others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
C | CAAA | 6 | a0001c0001t0002g0117a0001c0001t0007g0221a0001c0001t0009g0110others(3): Show | 6 | HG01257.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1042-1789_1042-178 others(7): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
C | CAAAA | 50 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1042-1790_1042-178 others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
C | CAAAAA | 13 | a0001c0001t0002g0058a0001c0001t0002g0068a0001c0001t0002g0070others(10): Show | 13 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1042-1791_1042-178 others(9): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
CA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1042-1787delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
CAA | C | 9 | a0001c0001t0004g0030a0001c0001t0004g0232a0001c0001t0010g0035others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1042-1788_1042-178 others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1042-1797_1042-178 others(15): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30685985
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0003g0250a0001c0001t0003g0294a0001c0001t0003g0295others(2): Show | 5 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1798_1042-178 others(16): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | ||||||
| chr8:30686118
|
C | T | 3 | a0001c0001t0007g0209a0001c0001t0007g0220a0001c0001t0007g0222 | 3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1042-1919G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686118 | ||||||
| chr8:30686221
|
T | A | 1 | a0001c0001t0030g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1042-2022A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686221 | ||||||
| chr8:30686221
|
T | C | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1042-2022A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686221 | ||||||
| chr8:30686690
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1041+2471T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686690 | ||||||
| chr8:30686702
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1041+2459G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686702 | ||||||
| chr8:30686703
|
A | C | 68 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0053others(65): Show | 68 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1041+2458T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686703 | ||||||
| chr8:30686704
|
A | C | 2 | a0001c0001t0002g0286a0006c0007t0001g0173 | 2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1041+2457T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686704 | ||||||
| chr8:30686841
|
G | GT | 8 | a0001c0001t0001g0228a0001c0001t0002g0058a0001c0001t0003g0260others(5): Show | 8 | HG01175.hp2 HG01978.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1041+2319dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686841 | ||||||
| chr8:30686841
|
G | T | 1 | a0001c0001t0003g0251 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1041+2320C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686841 | ||||||
| chr8:30686885
|
G | A | 3 | a0001c0001t0003g0250a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1041+2276C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686885 | ||||||
| chr8:30686897
|
C | T | 3 | a0001c0001t0002g0117a0001c0001t0002g0199a0001c0001t0036g0197 | 3 | HG02738.hp1 HG04115.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1041+2264G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686897 | ||||||
| chr8:30686997
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1041+2164A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686997 | ||||||
| chr8:30687046
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1041+2115T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687046 | ||||||
| chr8:30687129
|
G | A | 1 | a0001c0001t0049g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041+2032C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687129 | ||||||
| chr8:30687206
|
T | C | 1 | a0001c0001t0033g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1041+1955A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687206 | ||||||
| chr8:30687374
|
A | AG | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1786dupC | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687374 | ||||||
| chr8:30687413
|
C | T | 2 | a0001c0001t0010g0035a0002c0002t0004g0320 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1041+1748G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687413 | ||||||
| chr8:30687429
|
T | G | 3 | a0001c0001t0003g0250a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1041+1732A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687429 | ||||||
| chr8:30687444
|
G | A | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1041+1717C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687444 | ||||||
| chr8:30687520
|
C | T | 45 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0025others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1041+1641G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687520 | ||||||
| chr8:30687621
|
T | C | 2 | a0002c0002t0001g0331a0002c0002t0001g0333 | 2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1041+1540A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687621 | ||||||
| chr8:30687647
|
A | AAAAC | 6 | a0001c0001t0006g0263a0001c0001t0006g0265a0001c0001t0006g0266others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041+1510_1041+151 others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687647 | ||||||
| chr8:30687755
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1041+1406A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687755 | ||||||
| chr8:30687800
|
T | C | 1 | a0004c0005t0044g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1041+1361A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687800 | ||||||
| chr8:30688134
|
C | T | 4 | a0001c0001t0012g0216a0001c0003t0012g0011a0001c0004t0012g0323others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+1027G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688134 | ||||||
| chr8:30688221
|
A | C | 1 | a0002c0010t0015g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1041+940T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688221 | ||||||
| chr8:30688245
|
C | T | 4 | a0001c0003t0025g0009a0001c0003t0025g0010a0001c0003t0042g0007others(1): Show | 4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+916G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688245 | ||||||
| chr8:30688310
|
G | A | 72 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(69): Show | 72 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1041+851C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688310 | ||||||
| chr8:30688513
|
A | C | 1 | a0001c0001t0009g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1041+648T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688513 | ||||||
| chr8:30688578
|
C | CA | 85 | a0001c0001t0002g0060a0001c0001t0002g0224a0001c0001t0004g0013others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1041+582dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | ||||||
| chr8:30688578
|
C | CAA | 99 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 100 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1041+581_1041+582d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | ||||||
| chr8:30688578
|
C | CAAA | 10 | a0001c0001t0001g0128a0001c0001t0001g0156a0001c0001t0001g0244others(7): Show | 10 | HG00408.hp1 HG00621.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+580_1041+582d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | ||||||
| chr8:30688578
|
CA | C | 71 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(68): Show | 71 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1041+582delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | ||||||
| chr8:30688600
|
G | A | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1041+561C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688600 | ||||||
| chr8:30688714
|
G | A | 1 | a0001c0001t0035g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1041+447C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688714 | ||||||
| chr8:30688963
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1041+198T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688963 | ||||||
| chr8:30689041
|
T | C | 1 | a0001c0001t0003g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1041+120A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30689041 | ||||||
| chr8:30689119
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(196): Show | 200 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1041+42A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30689119 | ||||||
| chr8:30689324
|
T | G | 1 | a0001c0001t0002g0112 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.883-5A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689324 | ||||||
| chr8:30689449
|
G | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.883-130C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689449 | ||||||
| chr8:30689746
|
G | GTA | 12 | a0001c0001t0002g0224a0001c0001t0003g0223a0001c0001t0006g0136others(9): Show | 12 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.883-429_883-428dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689746 | ||||||
| chr8:30689746
|
GTA | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(261): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.883-429_883-428del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689746 | ||||||
| chr8:30689750
|
A | G | 4 | a0001c0001t0012g0216a0001c0003t0012g0011a0001c0004t0012g0323others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-431T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689750 | ||||||
| chr8:30689773
|
T | C | 4 | a0001c0001t0012g0216a0001c0003t0012g0011a0001c0004t0012g0323others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-454A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689773 | ||||||
| chr8:30689897
|
AT | A | 3 | a0001c0001t0004g0030a0001c0001t0004g0232a0001c0001t0004g0314 | 3 | HG02559.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-579delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689897 | ||||||
| chr8:30689923
|
GT | G | 6 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-605delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689923 | ||||||
| chr8:30689968
|
TTA | T | 5 | a0001c0001t0004g0030a0001c0001t0004g0065a0001c0001t0004g0232others(2): Show | 5 | HG02559.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-651_883-650del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689968 | ||||||
| chr8:30689984
|
A | ATATATAT others(37): Show |
2 | a0001c0001t0017g0033a0001c0001t0017g0038 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.883-666_883-665ins others(44): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689984 | ||||||
| chr8:30690006
|
ATATAT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.883-692_883-688del others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690006 | ||||||
| chr8:30690022
|
G | A | 25 | a0001c0001t0002g0316a0001c0001t0004g0030a0001c0001t0004g0232others(22): Show | 25 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-703C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690022 | ||||||
| chr8:30690029
|
T | C | 3 | a0001c0001t0004g0030a0001c0001t0004g0232a0001c0001t0004g0314 | 3 | HG02559.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-710A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690029 | ||||||
| chr8:30690046
|
TATAA | T | 6 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-731_883-728del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690046 | ||||||
| chr8:30690073
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.883-754G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690073 | ||||||
| chr8:30690098
|
TAAA | T | 4 | a0001c0001t0002g0316a0001c0001t0018g0215a0001c0001t0049g0034others(1): Show | 4 | HG02257.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-782_883-780del others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690098 | ||||||
| chr8:30690141
|
C | T | 1 | a0001c0001t0004g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.883-822G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690141 | ||||||
| chr8:30690155
|
A | AATTT | 5 | a0001c0001t0002g0286a0001c0001t0009g0147a0002c0002t0003g0334others(2): Show | 5 | HG00323.hp2 HG00738.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-837_883-836ins others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690155 | ||||||
| chr8:30690158
|
A | ATATT | 223 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.883-843_883-840dup others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690158 | ||||||
| chr8:30690158
|
A | T | 5 | a0001c0001t0002g0286a0001c0001t0009g0147a0002c0002t0003g0334others(2): Show | 5 | HG00323.hp2 HG00738.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-839T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690158 | ||||||
| chr8:30690541
|
G | A | 10 | a0001c0001t0005g0203a0001c0001t0005g0278a0001c0001t0005g0279others(7): Show | 10 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-1222C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690541 | ||||||
| chr8:30690637
|
G | A | 60 | a0001c0001t0003g0002a0001c0001t0003g0106a0001c0001t0003g0113others(57): Show | 61 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.883-1318C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690637 | ||||||
| chr8:30690906
|
A | T | 1 | a0001c0001t0002g0201 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.883-1587T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690906 | ||||||
| chr8:30690907
|
T | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0198a0001c0001t0002g0150others(1): Show | 4 | HG00408.hp2 HG00621.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1588A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690907 | ||||||
| chr8:30690947
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.883-1628T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690947 | ||||||
| chr8:30691180
|
A | G | 5 | a0001c0001t0003g0002a0001c0001t0003g0242a0001c0001t0003g0253others(2): Show | 6 | HG00099.hp1 HG00735.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+1789T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691180 | ||||||
| chr8:30691227
|
C | T | 3 | a0001c0001t0022g0205a0001c0001t0022g0211a0001c0003t0012g0012 | 3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.882+1742G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691227 | ||||||
| chr8:30691281
|
G | T | 1 | a0001c0001t0036g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.882+1688C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691281 | ||||||
| chr8:30691282
|
G | C | 1 | a0001c0001t0036g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.882+1687C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691282 | ||||||
| chr8:30691321
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.882+1648G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691321 | ||||||
| chr8:30692079
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0299 | 2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.882+890C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692079 | ||||||
| chr8:30692108
|
G | GA | 11 | a0001c0001t0008g0037a0001c0001t0008g0040a0001c0001t0008g0041others(8): Show | 11 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+860dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692108 | ||||||
| chr8:30692108
|
GA | G | 67 | a0001c0001t0003g0002a0001c0001t0003g0106a0001c0001t0003g0113others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.882+860delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692108 | ||||||
| chr8:30692181
|
G | GT | 345 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(342): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.882+787_882+788ins others(1): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692181 | ||||||
| chr8:30692196
|
C | CT | 109 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0052others(106): Show | 110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.882+772dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | ||||||
| chr8:30692196
|
C | CTT | 44 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0063others(41): Show | 44 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+771_882+772dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | ||||||
| chr8:30692196
|
C | CTTT | 7 | a0001c0001t0002g0199a0001c0001t0007g0217a0001c0001t0007g0219others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+770_882+772dup others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | ||||||
| chr8:30692196
|
CT | C | 14 | a0001c0001t0002g0316a0001c0001t0003g0253a0001c0001t0004g0314others(11): Show | 14 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+772delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | ||||||
| chr8:30692196
|
CTT | C | 18 | a0001c0001t0004g0030a0001c0001t0004g0232a0001c0001t0008g0037others(15): Show | 18 | HG01934.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.882+771_882+772del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | ||||||
| chr8:30692253
|
G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.882+716C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692253 | ||||||
| chr8:30692268
|
A | C | 1 | a0001c0001t0008g0037 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.882+701T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692268 | ||||||
| chr8:30692368
|
GT | G | 7 | a0001c0001t0002g0224a0001c0001t0007g0217a0001c0001t0007g0219others(4): Show | 7 | HG02280.hp2 HG02559.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+600delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692368 | ||||||
| chr8:30692495
|
C | CT | 197 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.882+473dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692495 | ||||||
| chr8:30692495
|
C | CTT | 102 | a0001c0001t0001g0082a0001c0001t0001g0096a0001c0001t0001g0098others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.882+472_882+473dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692495 | ||||||
| chr8:30692495
|
C | CTTT | 14 | a0001c0001t0003g0139a0001c0001t0003g0241a0001c0001t0003g0251others(11): Show | 14 | HG00735.hp1 HG01081.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+471_882+473dup others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692495 | ||||||
| chr8:30692857
|
A | C | 1 | a0001c0001t0006g0269 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+112T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692857 | ||||||
| chr8:30693144
|
A | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.796-89T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693144 | ||||||
| chr8:30693245
|
T | C | 1 | a0001c0001t0026g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.796-190A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693245 | ||||||
| chr8:30693399
|
T | C | 2 | a0001c0001t0017g0033a0001c0001t0017g0038 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.796-344A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693399 | ||||||
| chr8:30693416
|
T | C | 4 | a0001c0001t0012g0216a0001c0003t0012g0011a0001c0004t0012g0323others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-361A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693416 | ||||||
| chr8:30693533
|
A | AT | 5 | a0001c0001t0006g0136a0001c0001t0006g0269a0001c0001t0026g0167others(2): Show | 5 | HG02630.hp1 HG03492.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.796-479dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693533 | ||||||
| chr8:30693533
|
A | ATG | 4 | a0001c0003t0025g0009a0001c0003t0042g0007a0001c0004t0014g0319others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-479_796-478ins others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693533 | ||||||
| chr8:30693534
|
T | C | 1 | a0002c0002t0011g0341 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.796-479A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693534 | ||||||
| chr8:30693538
|
T | C | 1 | a0001c0001t0004g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.796-483A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693538 | ||||||
| chr8:30693538
|
TA | T | 6 | a0001c0001t0001g0105a0001c0001t0001g0119a0001c0001t0002g0188others(3): Show | 6 | HG00323.hp1 HG00558.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-484delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693538 | ||||||
| chr8:30693539
|
A | T | 339 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.796-484T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693539 | ||||||
| chr8:30693696
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(254): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.796-641G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693696 | ||||||
| chr8:30694182
|
C | T | 1 | a0001c0001t0014g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.796-1127G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694182 | ||||||
| chr8:30694291
|
G | A | 1 | a0001c0001t0011g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.796-1236C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694291 | ||||||
| chr8:30694443
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.796-1388C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694443 | ||||||
| chr8:30694544
|
T | G | 2 | a0001c0001t0002g0117a0001c0001t0004g0133 | 2 | NA18986.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.796-1489A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694544 | ||||||
| chr8:30694882
|
A | G | 2 | a0001c0001t0029g0032a0001c0001t0032g0031 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.795+1498T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694882 | ||||||
| chr8:30694897
|
C | CA | 91 | a0001c0001t0001g0146a0001c0001t0003g0002a0001c0001t0003g0106others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.795+1482dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694897 | ||||||
| chr8:30694897
|
C | CAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 110 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.795+1481_795+1482d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694897 | ||||||
| chr8:30694897
|
C | CAAA | 10 | a0001c0001t0001g0052a0001c0001t0002g0050a0001c0001t0002g0051others(7): Show | 10 | HG01069.hp1 HG01123.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+1480_795+1482d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694897 | ||||||
| chr8:30694986
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.795+1394T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694986 | ||||||
| chr8:30695112
|
T | C | 1 | a0002c0002t0020g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.795+1268A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695112 | ||||||
| chr8:30695176
|
C | T | 22 | a0001c0001t0005g0203a0001c0001t0005g0207a0001c0001t0005g0208others(19): Show | 22 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.795+1204G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695176 | ||||||
| chr8:30695183
|
A | T | 22 | a0001c0001t0005g0203a0001c0001t0005g0207a0001c0001t0005g0208others(19): Show | 22 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.795+1197T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695183 | ||||||
| chr8:30695276
|
C | T | 3 | a0001c0001t0006g0136a0001c0001t0006g0269a0001c0004t0006g0332 | 3 | HG02630.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.795+1104G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695276 | ||||||
| chr8:30695290
|
C | A | 3 | a0001c0001t0022g0205a0001c0001t0022g0211a0001c0003t0012g0012 | 3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.795+1090G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695290 | ||||||
| chr8:30695482
|
C | T | 2 | a0003c0006t0009g0343a0003c0006t0018g0344 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.795+898G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695482 | ||||||
| chr8:30695485
|
C | T | 3 | a0001c0001t0006g0136a0001c0001t0006g0269a0001c0004t0006g0332 | 3 | HG02630.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.795+895G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695485 | ||||||
| chr8:30695522
|
A | C | 1 | a0001c0001t0007g0075 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.795+858T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695522 | ||||||
| chr8:30695697
|
G | A | 2 | a0001c0003t0025g0009a0001c0003t0025g0010 | 2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.795+683C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695697 | ||||||
| chr8:30695780
|
C | G | 3 | a0001c0001t0004g0071a0001c0001t0004g0189a0001c0009t0001g0027 | 3 | NA18964.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.795+600G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695780 | ||||||
| chr8:30695813
|
G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795+567C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695813 | ||||||
| chr8:30695913
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.795+467T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695913 | ||||||
| chr8:30695951
|
A | T | 1 | a0001c0001t0004g0155 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.795+429T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695951 | ||||||
| chr8:30695954
|
C | T | 4 | a0001c0001t0002g0316a0001c0001t0020g0168a0001c0001t0020g0169others(1): Show | 4 | HG02055.hp1 NA19030.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+426G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695954 | ||||||
| chr8:30696114
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0165 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.795+266C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30696114 | ||||||
| chr8:30696283
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.795+97G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30696283 | ||||||
| chr8:30696489
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 139 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.696-10C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696489 | ||||||
| chr8:30696656
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.696-177G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696656 | ||||||
| chr8:30696749
|
G | A | 12 | a0001c0001t0002g0224a0001c0001t0003g0223a0001c0001t0006g0136others(9): Show | 12 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.696-270C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696749 | ||||||
| chr8:30696827
|
C | A | 2 | a0002c0002t0001g0331a0002c0002t0001g0333 | 2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.696-348G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696827 | ||||||
| chr8:30697211
|
C | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.696-732G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697211 | ||||||
| chr8:30697241
|
C | T | 3 | a0001c0001t0006g0136a0001c0001t0006g0269a0001c0004t0006g0332 | 3 | HG02630.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.696-762G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697241 | ||||||
| chr8:30697367
|
T | C | 9 | a0001c0001t0002g0224a0001c0001t0003g0223a0001c0001t0007g0217others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-888A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697367 | ||||||
| chr8:30697408
|
T | C | 2 | a0001c0001t0029g0032a0001c0001t0032g0031 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.696-929A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697408 | ||||||
| chr8:30697421
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 136 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.696-942G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697421 | ||||||
| chr8:30697422
|
A | AAAAC | 80 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0046others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.696-947_696-944dup others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697422 | ||||||
| chr8:30697422
|
AAAAC | A | 11 | a0001c0001t0003g0285a0001c0001t0004g0298a0001c0001t0012g0216others(8): Show | 11 | HG02451.hp1 HG02602.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.696-947_696-944del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697422 | ||||||
| chr8:30697425
|
A | AAC | 9 | a0001c0001t0008g0037a0001c0001t0008g0041a0001c0001t0008g0042others(6): Show | 9 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-947_696-946ins others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697425 | ||||||
| chr8:30697426
|
C | A | 10 | a0001c0001t0008g0037a0001c0001t0008g0040a0001c0001t0008g0041others(7): Show | 10 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-947G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697426 | ||||||
| chr8:30697426
|
C | CA | 127 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(124): Show | 128 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.696-948dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697426 | ||||||
| chr8:30697429
|
A | C | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.696-950T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697429 | ||||||
| chr8:30697430
|
C | A | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.696-951G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697430 | ||||||
| chr8:30697567
|
G | GCAGTGAG others(1): Show |
3 | a0001c0001t0022g0205a0001c0001t0022g0211a0001c0003t0012g0012 | 3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.696-1096_696-1089d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697567 | ||||||
| chr8:30697826
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.696-1347G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697826 | ||||||
| chr8:30697933
|
C | T | 4 | a0001c0001t0015g0066a0001c0001t0022g0205a0001c0001t0022g0211others(1): Show | 4 | HG00597.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1454G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697933 | ||||||
| chr8:30697973
|
T | A | 1 | a0003c0006t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.696-1494A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697973 | ||||||
| chr8:30698080
|
A | G | 1 | a0001c0001t0022g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.696-1601T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698080 | ||||||
| chr8:30698081
|
C | T | 6 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1602G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698081 | ||||||
| chr8:30698098
|
C | T | 2 | a0001c0001t0005g0208a0001c0001t0007g0209 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.696-1619G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698098 | ||||||
| chr8:30698224
|
G | A | 1 | a0001c0003t0025g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.696-1745C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698224 | ||||||
| chr8:30698413
|
G | A | 1 | a0001c0001t0009g0110 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.695+1668C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698413 | ||||||
| chr8:30698416
|
A | G | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.695+1665T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698416 | ||||||
| chr8:30698492
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.695+1589C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698492 | ||||||
| chr8:30698516
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(342): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.695+1565A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698516 | ||||||
| chr8:30698576
|
A | G | 8 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(5): Show | 8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+1505T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698576 | ||||||
| chr8:30698638
|
C | T | 1 | a0003c0006t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695+1443G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698638 | ||||||
| chr8:30698864
|
T | TCC | 116 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0045others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.695+1215_695+1216d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698864 | ||||||
| chr8:30698876
|
C | T | 1 | a0001c0001t0034g0159 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.695+1205G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698876 | ||||||
| chr8:30698884
|
A | C | 8 | a0001c0001t0002g0224a0001c0001t0003g0223a0001c0001t0007g0217others(5): Show | 8 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+1197T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698884 | ||||||
| chr8:30699094
|
T | C | 116 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0045others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.695+987A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699094 | ||||||
| chr8:30699265
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.695+816A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699265 | ||||||
| chr8:30699292
|
A | T | 88 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0046others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.695+789T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699292 | ||||||
| chr8:30699312
|
A | T | 14 | a0001c0001t0008g0037a0001c0001t0008g0040a0001c0001t0008g0041others(11): Show | 14 | HG01243.hp2 HG01934.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695+769T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699312 | ||||||
| chr8:30699361
|
C | T | 1 | a0001c0001t0006g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.695+720G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699361 | ||||||
| chr8:30699448
|
A | G | 2 | a0002c0002t0019g0321a0002c0002t0020g0322 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.695+633T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699448 | ||||||
| chr8:30699591
|
A | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(342): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.695+490T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699591 | ||||||
| chr8:30700190
|
T | C | 2 | a0001c0001t0004g0232a0001c0001t0004g0314 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.641-55A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700190 | ||||||
| chr8:30700454
|
G | A | 1 | a0001c0001t0009g0186 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.641-319C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700454 | ||||||
| chr8:30700481
|
C | T | 1 | a0001c0001t0005g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.641-346G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700481 | ||||||
| chr8:30700530
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0165 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.641-395G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700530 | ||||||
| chr8:30700648
|
T | C | 1 | a0003c0006t0012g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.641-513A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700648 | ||||||
| chr8:30700722
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0161 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.641-588_641-587ins others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700722 | ||||||
| chr8:30700722
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0223a0001c0001t0007g0221 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.641-588_641-587ins others(11): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700722 | ||||||
| chr8:30700722
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0007g0059a0001c0001t0007g0217a0001c0001t0007g0219others(3): Show | 6 | HG02280.hp2 HG03486.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-588_641-587ins others(12): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700722 | ||||||
| chr8:30700723
|
C | A | 11 | a0001c0001t0002g0161a0001c0001t0002g0224a0001c0001t0003g0223others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.641-588G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0023a0001c0001t0001g0098a0001c0001t0001g0175others(12): Show | 15 | HG01515.hp1 HG01934.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.641-596_641-589dup others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(2): Show |
14 | a0001c0001t0001g0109a0001c0001t0001g0119a0001c0001t0001g0120others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.641-597_641-589dup others(9): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(3): Show |
32 | a0001c0001t0001g0124a0001c0001t0002g0056a0001c0001t0002g0060others(29): Show | 32 | HG00558.hp2 HG01074.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.641-598_641-589dup others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(4): Show |
38 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 39 | HG00597.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.641-599_641-589dup others(11): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(5): Show |
21 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0130others(18): Show | 21 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-600_641-589dup others(12): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0132others(5): Show | 8 | HG01261.hp2 HG01361.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-601_641-589dup others(13): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0004g0133a0001c0001t0030g0179 | 2 | NA19011.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.641-602_641-589dup others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.641-607_641-589dup others(19): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0010g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.641-612_641-589dup others(24): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
CAAAA | C | 7 | a0001c0001t0001g0146a0001c0001t0004g0087a0001c0001t0004g0226others(4): Show | 7 | HG00621.hp2 HG00673.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-592_641-589del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
CAAAAA | C | 61 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.641-593_641-589del others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
CAAAAAA | C | 36 | a0001c0001t0001g0299a0001c0001t0004g0065a0001c0001t0005g0203others(33): Show | 36 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.641-594_641-589del others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
CAAAAAAA | C | 14 | a0001c0001t0002g0058a0001c0001t0002g0107a0001c0001t0002g0116others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-595_641-589del others(7): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
CAAAAAAA others(1): Show |
C | 62 | a0001c0001t0001g0252a0001c0001t0002g0054a0001c0001t0002g0102others(59): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.641-596_641-589del others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30700723
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.641-601_641-589del others(13): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | ||||||
| chr8:30701022
|
C | G | 1 | a0001c0001t0003g0106 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.641-887G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701022 | ||||||
| chr8:30701114
|
T | C | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.641-979A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701114 | ||||||
| chr8:30701334
|
C | T | 1 | a0001c0001t0006g0264 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.641-1199G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701334 | ||||||
| chr8:30701337
|
A | G | 1 | a0001c0001t0006g0264 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.641-1202T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701337 | ||||||
| chr8:30701370
|
G | A | 21 | a0001c0001t0005g0208a0001c0001t0005g0278a0001c0001t0005g0279others(18): Show | 21 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-1235C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701370 | ||||||
| chr8:30701488
|
A | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.641-1353T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701488 | ||||||
| chr8:30701571
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.641-1436T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701571 | ||||||
| chr8:30701605
|
C | T | 4 | a0001c0003t0005g0008a0001c0003t0025g0009a0001c0003t0025g0010others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-1470G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701605 | ||||||
| chr8:30701606
|
G | A | 2 | a0001c0001t0009g0110a0001c0001t0030g0179 | 2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.641-1471C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701606 | ||||||
| chr8:30701635
|
C | CA | 120 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(117): Show | 121 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.640+1457dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701635 | ||||||
| chr8:30701717
|
C | T | 36 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.640+1376G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701717 | ||||||
| chr8:30701718
|
G | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0200a0001c0001t0015g0154others(1): Show | 4 | HG00639.hp1 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+1375C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701718 | ||||||
| chr8:30701749
|
C | T | 2 | a0001c0001t0004g0065a0001c0001t0004g0086 | 2 | HG02273.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.640+1344G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701749 | ||||||
| chr8:30701794
|
C | CA | 12 | a0001c0001t0002g0224a0001c0001t0004g0030a0001c0001t0004g0232others(9): Show | 12 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+1298dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701794 | ||||||
| chr8:30701794
|
CA | C | 152 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0029others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.640+1298delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701794 | ||||||
| chr8:30701794
|
CAA | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0052others(153): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.640+1297_640+1298d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701794 | ||||||
| chr8:30702010
|
T | C | 1 | a0001c0001t0007g0135 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.640+1083A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702010 | ||||||
| chr8:30702098
|
C | T | 13 | a0001c0001t0008g0037a0001c0001t0008g0040a0001c0001t0008g0041others(10): Show | 13 | HG01243.hp2 HG01934.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+995G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702098 | ||||||
| chr8:30702522
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.640+571A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702522 | ||||||
| chr8:30702632
|
T | C | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.640+461A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702632 | ||||||
| chr8:30702671
|
G | A | 48 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(45): Show | 48 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+422C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702671 | ||||||
| chr8:30703244
|
A | C | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.493-4T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703244 | ||||||
| chr8:30703294
|
T | C | 1 | a0001c0001t0002g0286 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.493-54A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703294 | ||||||
| chr8:30703370
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 123 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.493-130G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703370 | ||||||
| chr8:30703389
|
G | C | 1 | a0001c0001t0002g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.493-149C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703389 | ||||||
| chr8:30703502
|
T | A | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.493-262A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703502 | ||||||
| chr8:30703782
|
C | G | 48 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(45): Show | 48 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.493-542G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703782 | ||||||
| chr8:30703914
|
G | C | 1 | a0003c0006t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.493-674C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703914 | ||||||
| chr8:30704008
|
G | A | 2 | a0001c0001t0005g0249a0001c0001t0010g0248 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.493-768C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704008 | ||||||
| chr8:30704090
|
C | T | 8 | a0001c0001t0002g0224a0001c0001t0003g0223a0001c0001t0007g0217others(5): Show | 8 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-850G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704090 | ||||||
| chr8:30704228
|
G | A | 1 | a0001c0001t0018g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.493-988C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704228 | ||||||
| chr8:30704444
|
T | C | 3 | a0001c0001t0014g0019a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.493-1204A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704444 | ||||||
| chr8:30704503
|
C | T | 35 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.493-1263G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704503 | ||||||
| chr8:30704549
|
T | C | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-1309A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704549 | ||||||
| chr8:30704604
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 112 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.493-1364G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704604 | ||||||
| chr8:30704721
|
T | C | 1 | a0001c0001t0013g0293 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493-1481A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704721 | ||||||
| chr8:30704952
|
A | G | 1 | a0001c0001t0019g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.493-1712T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704952 | ||||||
| chr8:30704959
|
T | C | 1 | a0001c0001t0013g0293 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493-1719A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704959 | ||||||
| chr8:30705131
|
TA | T | 35 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.493-1892delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705131 | ||||||
| chr8:30705262
|
C | CA | 339 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.493-2023dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705262 | ||||||
| chr8:30705270
|
T | A | 38 | a0001c0001t0001g0082a0001c0001t0002g0286a0001c0001t0002g0296others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.493-2030A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705270 | ||||||
| chr8:30705313
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 115 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.493-2073T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705313 | ||||||
| chr8:30705319
|
G | C | 1 | a0001c0001t0004g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.493-2079C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705319 | ||||||
| chr8:30705372
|
C | T | 2 | a0001c0001t0005g0249a0001c0001t0010g0248 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.493-2132G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705372 | ||||||
| chr8:30705437
|
A | AT | 4 | a0001c0001t0005g0315a0001c0001t0024g0212a0001c0001t0024g0213others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-2198dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705437 | ||||||
| chr8:30705508
|
C | T | 3 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0237 | 3 | HG02258.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.493-2268G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705508 | ||||||
| chr8:30705554
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.493-2314C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705554 | ||||||
| chr8:30705694
|
T | G | 5 | a0001c0001t0002g0316a0004c0005t0010g0005a0004c0005t0043g0003others(2): Show | 5 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+2378A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705694 | ||||||
| chr8:30705750
|
A | G | 3 | a0001c0001t0012g0216a0001c0003t0012g0011a0003c0006t0012g0342 | 3 | HG02451.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.492+2322T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705750 | ||||||
| chr8:30705925
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.492+2147G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705925 | ||||||
| chr8:30706023
|
G | A | 1 | a0001c0001t0016g0262 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.492+2049C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706023 | ||||||
| chr8:30706174
|
CA | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0002g0102others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.492+1897delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706174 | ||||||
| chr8:30706174
|
CAA | C | 6 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0287others(3): Show | 6 | HG00738.hp1 HG02965.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+1896_492+1897d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706174 | ||||||
| chr8:30706366
|
G | C | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.492+1706C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706366 | ||||||
| chr8:30706383
|
G | C | 5 | a0001c0001t0002g0316a0004c0005t0010g0005a0004c0005t0043g0003others(2): Show | 5 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+1689C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706383 | ||||||
| chr8:30706393
|
C | T | 1 | a0001c0001t0018g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.492+1679G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706393 | ||||||
| chr8:30706395
|
C | T | 3 | a0001c0001t0016g0308a0001c0001t0016g0310a0001c0001t0040g0309 | 3 | HG03834.hp2 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.492+1677G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706395 | ||||||
| chr8:30706508
|
T | TAAAC | 14 | a0002c0002t0001g0324a0002c0002t0001g0325a0002c0002t0001g0327others(11): Show | 14 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.492+1560_492+1563d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706508 | ||||||
| chr8:30706508
|
TAAAC | T | 3 | a0001c0001t0004g0092a0001c0001t0035g0100a0001c0003t0015g0006 | 3 | HG00438.hp1 HG00733.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.492+1560_492+1563d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706508 | ||||||
| chr8:30706537
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.492+1535C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706537 | ||||||
| chr8:30706591
|
G | A | 1 | a0001c0001t0048g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.492+1481C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706591 | ||||||
| chr8:30706874
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.492+1198G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706874 | ||||||
| chr8:30706890
|
A | G | 1 | a0001c0001t0004g0071 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.492+1182T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706890 | ||||||
| chr8:30706954
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0299 | 2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.492+1118C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706954 | ||||||
| chr8:30707219
|
C | A | 1 | a0001c0001t0049g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492+853G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707219 | ||||||
| chr8:30707226
|
A | G | 1 | a0001c0001t0049g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492+846T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707226 | ||||||
| chr8:30707270
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.492+802C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707270 | ||||||
| chr8:30707680
|
T | C | 334 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(331): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.492+392A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707680 | ||||||
| chr8:30707730
|
A | G | 139 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0045others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.492+342T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707730 | ||||||
| chr8:30707734
|
C | A | 11 | a0001c0001t0002g0224a0001c0001t0003g0223a0001c0001t0005g0203others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.492+338G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707734 | ||||||
| chr8:30707765
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.492+307C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707765 | ||||||
| chr8:30708035
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.492+37G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30708035 | ||||||
| chr8:30708245
|
T | C | 1 | a0001c0003t0025g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.423-104A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708245 | ||||||
| chr8:30708258
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.423-117G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708258 | ||||||
| chr8:30708367
|
A | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(331): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.423-226T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708367 | ||||||
| chr8:30708376
|
C | T | 4 | a0004c0005t0010g0005a0004c0005t0043g0003a0004c0005t0044g0004others(1): Show | 4 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-235G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708376 | ||||||
| chr8:30708377
|
G | A | 35 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.423-236C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708377 | ||||||
| chr8:30708428
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.423-287G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708428 | ||||||
| chr8:30708488
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.423-347T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708488 | ||||||
| chr8:30708493
|
T | C | 34 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(31): Show | 34 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.423-352A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708493 | ||||||
| chr8:30708646
|
T | C | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423-505A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708646 | ||||||
| chr8:30708691
|
T | C | 6 | a0001c0001t0002g0070a0001c0001t0002g0185a0001c0001t0002g0188others(3): Show | 6 | HG00558.hp2 HG00735.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-550A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708691 | ||||||
| chr8:30708750
|
A | C | 1 | a0001c0001t0003g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.423-609T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708750 | ||||||
| chr8:30708760
|
T | C | 4 | a0001c0003t0005g0008a0001c0003t0025g0009a0001c0003t0025g0010others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-619A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708760 | ||||||
| chr8:30708831
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.423-690A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708831 | ||||||
| chr8:30708833
|
C | A | 1 | a0001c0001t0036g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.423-692G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708833 | ||||||
| chr8:30708958
|
C | CA | 31 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(28): Show | 31 | HG00621.hp2 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.423-818dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708958 | ||||||
| chr8:30709192
|
T | C | 38 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(35): Show | 39 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.422+622A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709192 | ||||||
| chr8:30709222
|
A | G | 1 | a0001c0001t0004g0184 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.422+592T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709222 | ||||||
| chr8:30709225
|
C | T | 42 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(39): Show | 43 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.422+589G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709225 | ||||||
| chr8:30709269
|
G | A | 41 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(38): Show | 42 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.422+545C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709269 | ||||||
| chr8:30709269
|
G | T | 30 | a0001c0001t0003g0210a0001c0001t0005g0207a0001c0001t0005g0208others(27): Show | 30 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.422+545C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709269 | ||||||
| chr8:30709271
|
G | A | 1 | a0001c0001t0004g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.422+543C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709271 | ||||||
| chr8:30709331
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.422+483G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709331 | ||||||
| chr8:30709612
|
T | A | 5 | a0001c0001t0002g0076a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.422+202A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709612 | ||||||
| chr8:30709632
|
G | A | 4 | a0001c0001t0003g0218a0001c0001t0018g0215a0001c0004t0003g0339others(1): Show | 4 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+182C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709632 | ||||||
| chr8:30709700
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0104 | 3 | HG00639.hp2 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.422+114C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709700 | ||||||
| chr8:30709762
|
A | C | 1 | a0001c0001t0002g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.422+52T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709762 | ||||||
| chr8:30709905
|
G | GT | 6 | a0001c0001t0002g0316a0003c0006t0018g0344a0004c0005t0010g0005others(3): Show | 6 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.334-4dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709905 | ||||||
| chr8:30709906
|
T | TA | 13 | a0001c0001t0002g0054a0001c0001t0002g0102a0001c0001t0002g0103others(10): Show | 13 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.334-5dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709906 | ||||||
| chr8:30709906
|
TA | T | 13 | a0001c0001t0001g0105a0001c0001t0003g0218a0001c0001t0012g0216others(10): Show | 13 | HG00323.hp1 HG01975.hp2 HG02257.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.334-5delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709906 | ||||||
| chr8:30709907
|
A | T | 3 | a0001c0003t0025g0009a0001c0003t0025g0010a0001c0003t0042g0007 | 3 | HG02886.hp1 HG02886.hp2 HG03225.hp2 |
splice_region_variant&intron_variant | LOW | c.334-5T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709907 | ||||||
| chr8:30709908
|
A | T | 1 | a0001c0003t0005g0008 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.334-6T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709908 | ||||||
| chr8:30710011
|
C | T | 8 | a0001c0001t0005g0278a0001c0001t0005g0279a0001c0001t0005g0281others(5): Show | 8 | HG02280.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-109G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710011 | ||||||
| chr8:30710013
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.334-111G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710013 | ||||||
| chr8:30710044
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.334-142C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710044 | ||||||
| chr8:30710535
|
G | A | 3 | a0001c0001t0020g0168a0001c0001t0020g0169a0001c0001t0026g0167 | 3 | HG02055.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.334-633C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710535 | ||||||
| chr8:30710541
|
A | C | 11 | a0001c0001t0005g0249a0001c0001t0005g0278a0001c0001t0005g0279others(8): Show | 11 | HG02280.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-639T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710541 | ||||||
| chr8:30710687
|
G | A | 1 | a0001c0001t0029g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-785C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710687 | ||||||
| chr8:30710714
|
C | CA | 6 | a0001c0001t0003g0218a0001c0001t0005g0249a0001c0001t0005g0278others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-813dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
C | CAA | 6 | a0001c0001t0005g0282a0001c0001t0005g0283a0001c0001t0005g0284others(3): Show | 6 | HG02572.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-814_334-813dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CA | C | 12 | a0001c0001t0004g0232a0001c0001t0010g0035a0001c0001t0012g0216others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.334-813delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAA | C | 9 | a0001c0001t0002g0316a0001c0001t0004g0030a0001c0001t0005g0203others(6): Show | 9 | HG00738.hp2 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-814_334-813del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAAA | C | 32 | a0001c0001t0001g0029a0001c0001t0001g0084a0001c0001t0001g0098others(29): Show | 32 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.334-815_334-813del others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAAAA | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.334-816_334-813del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAAAAA | C | 39 | a0001c0001t0001g0104a0001c0001t0001g0164a0001c0001t0002g0286others(36): Show | 39 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.334-817_334-813del others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0002g0224a0001c0001t0007g0217a0001c0001t0007g0219others(4): Show | 7 | HG02280.hp2 HG02559.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.334-823_334-813del others(11): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0026g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334-829_334-813del others(17): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710714
|
CAAAAAAA others(13): Show |
C | 67 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(64): Show | 68 | HG00099.hp1 HG00621.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.334-832_334-813del others(20): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | ||||||
| chr8:30710741
|
A | G | 1 | a0001c0001t0021g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.334-839T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710741 | ||||||
| chr8:30710757
|
AAAG | A | 32 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(29): Show | 33 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.334-858_334-856del others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710757 | ||||||
| chr8:30710758
|
AAG | A | 32 | a0001c0001t0003g0210a0001c0001t0003g0240a0001c0001t0005g0207others(29): Show | 32 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.334-858_334-857del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710758 | ||||||
| chr8:30710764
|
A | T | 23 | a0001c0001t0002g0261a0001c0001t0003g0210a0001c0001t0003g0240others(20): Show | 23 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-862T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710764 | ||||||
| chr8:30710766
|
A | T | 54 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(51): Show | 55 | HG00099.hp1 HG00621.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.334-864T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710766 | ||||||
| chr8:30710768
|
A | AT | 5 | a0001c0001t0003g0218a0001c0001t0012g0216a0001c0001t0018g0215others(2): Show | 5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-867_334-866ins others(1): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710768 | ||||||
| chr8:30710768
|
A | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.334-866T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710768 | ||||||
| chr8:30710844
|
C | T | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.334-942G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710844 | ||||||
| chr8:30711117
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.333+945T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711117 | ||||||
| chr8:30711118
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.333+944G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711118 | ||||||
| chr8:30711120
|
G | A | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+942C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711120 | ||||||
| chr8:30711125
|
G | A | 2 | a0001c0001t0004g0078a0001c0001t0018g0077 | 2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.333+937C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711125 | ||||||
| chr8:30711173
|
G | A | 1 | a0001c0001t0011g0181 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.333+889C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711173 | ||||||
| chr8:30711252
|
G | A | 40 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0238others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.333+810C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711252 | ||||||
| chr8:30711498
|
T | A | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+564A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711498 | ||||||
| chr8:30711525
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.333+537G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711525 | ||||||
| chr8:30711594
|
G | A | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+468C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711594 | ||||||
| chr8:30711621
|
C | T | 2 | a0001c0001t0004g0232a0001c0001t0004g0314 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.333+441G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711621 | ||||||
| chr8:30711649
|
C | T | 1 | a0001c0004t0045g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.333+413G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711649 | ||||||
| chr8:30711650
|
G | A | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+412C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711650 | ||||||
| chr8:30711653
|
G | A | 40 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0238others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.333+409C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711653 | ||||||
| chr8:30711733
|
T | C | 1 | a0001c0001t0007g0225 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.333+329A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711733 | ||||||
| chr8:30712135
|
C | T | 5 | a0001c0001t0003g0218a0001c0001t0012g0216a0001c0001t0018g0215others(2): Show | 5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-47G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712135 | ||||||
| chr8:30712309
|
C | T | 5 | a0001c0001t0003g0218a0001c0001t0012g0216a0001c0001t0018g0215others(2): Show | 5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-221G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712309 | ||||||
| chr8:30712310
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.307-222C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712310 | ||||||
| chr8:30712350
|
G | A | 1 | a0001c0001t0035g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.307-262C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712350 | ||||||
| chr8:30712501
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0034g0159 | 2 | HG01884.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.307-413C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712501 | ||||||
| chr8:30712509
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.307-421C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712509 | ||||||
| chr8:30712553
|
G | A | 42 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0238others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.307-465C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712553 | ||||||
| chr8:30712607
|
AAGGCTGC others(11): Show |
A | 1 | a0001c0004t0005g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.307-537_307-520del others(18): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712607 | ||||||
| chr8:30712640
|
A | G | 2 | a0001c0001t0020g0168a0001c0001t0020g0169 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.307-552T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712640 | ||||||
| chr8:30712706
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307-618C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712706 | ||||||
| chr8:30712766
|
C | T | 1 | a0001c0001t0033g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.307-678G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712766 | ||||||
| chr8:30712768
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.307-680A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712768 | ||||||
| chr8:30712832
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.307-744A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712832 | ||||||
| chr8:30713065
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.307-977G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713065 | ||||||
| chr8:30713225
|
T | TG | 10 | a0001c0001t0002g0316a0001c0003t0005g0008a0001c0003t0025g0009others(7): Show | 10 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-1138dupC | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713225 | ||||||
| chr8:30713256
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0104 | 3 | HG00639.hp2 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.307-1168G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713256 | ||||||
| chr8:30713286
|
C | T | 5 | a0001c0001t0003g0218a0001c0001t0012g0216a0001c0001t0018g0215others(2): Show | 5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1198G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713286 | ||||||
| chr8:30713389
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(192): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.307-1301G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713389 | ||||||
| chr8:30713435
|
T | C | 2 | a0001c0001t0002g0161a0001c0001t0007g0059 | 2 | NA18964.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.307-1347A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713435 | ||||||
| chr8:30713585
|
A | T | 6 | a0001c0001t0002g0054a0001c0001t0002g0060a0001c0001t0002g0061others(3): Show | 6 | HG01952.hp1 HG02155.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1497T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713585 | ||||||
| chr8:30713658
|
C | T | 1 | a0001c0001t0006g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307-1570G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713658 | ||||||
| chr8:30713985
|
A | C | 13 | a0001c0001t0003g0210a0001c0001t0005g0207a0001c0001t0005g0208others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.307-1897T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713985 | ||||||
| chr8:30714180
|
C | T | 2 | a0002c0002t0001g0331a0002c0002t0001g0333 | 2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.307-2092G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714180 | ||||||
| chr8:30714202
|
C | CT | 21 | a0001c0001t0002g0316a0001c0001t0003g0251a0001c0001t0005g0278others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.307-2115dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714202 | ||||||
| chr8:30714202
|
CT | C | 98 | a0001c0001t0001g0045a0001c0001t0001g0057a0001c0001t0001g0096others(95): Show | 99 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.307-2115delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714202 | ||||||
| chr8:30714202
|
CTT | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.307-2116_307-2115d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714202 | ||||||
| chr8:30714294
|
C | T | 1 | a0001c0001t0016g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.307-2206G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714294 | ||||||
| chr8:30714395
|
C | T | 3 | a0001c0001t0002g0053a0001c0001t0002g0093a0001c0001t0002g0094 | 3 | HG00642.hp1 HG01099.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.307-2307G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714395 | ||||||
| chr8:30714446
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.307-2358G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714446 | ||||||
| chr8:30714488
|
A | G | 1 | a0001c0001t0004g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.307-2400T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714488 | ||||||
| chr8:30714504
|
C | T | 1 | a0001c0001t0010g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.307-2416G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714504 | ||||||
| chr8:30714509
|
T | A | 3 | a0001c0001t0003g0250a0001c0001t0003g0294a0001c0001t0003g0295 | 3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.307-2421A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714509 | ||||||
| chr8:30714668
|
C | A | 4 | a0001c0001t0005g0315a0001c0001t0024g0212a0001c0001t0024g0213others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-2580G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714668 | ||||||
| chr8:30714695
|
T | A | 1 | a0001c0001t0002g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.307-2607A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714695 | ||||||
| chr8:30714738
|
G | A | 2 | a0001c0004t0045g0330a0005c0008t0037g0204 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.307-2650C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714738 | ||||||
| chr8:30714824
|
C | T | 1 | a0001c0003t0042g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.307-2736G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714824 | ||||||
| chr8:30714973
|
T | A | 3 | a0001c0001t0022g0205a0001c0001t0022g0211a0001c0003t0012g0012 | 3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.307-2885A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714973 | ||||||
| chr8:30715013
|
C | T | 2 | a0001c0001t0004g0083a0001c0001t0004g0092 | 2 | HG00733.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.307-2925G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715013 | ||||||
| chr8:30715027
|
A | G | 43 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0238others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.307-2939T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715027 | ||||||
| chr8:30715061
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.307-2973A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715061 | ||||||
| chr8:30715198
|
C | T | 41 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0238others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.307-3110G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715198 | ||||||
| chr8:30715392
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0004g0163 | 2 | HG02015.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.307-3304C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715392 | ||||||
| chr8:30715572
|
C | T | 1 | a0001c0001t0004g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.307-3484G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715572 | ||||||
| chr8:30715574
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.307-3486A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715574 | ||||||
| chr8:30715583
|
G | A | 6 | a0001c0001t0005g0315a0001c0001t0006g0230a0001c0001t0024g0212others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-3495C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715583 | ||||||
| chr8:30715632
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.307-3544G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715632 | ||||||
| chr8:30715825
|
T | C | 5 | a0001c0003t0005g0008a0001c0003t0025g0009a0001c0003t0025g0010others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-3737A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715825 | ||||||
| chr8:30715890
|
T | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.307-3802A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715890 | ||||||
| chr8:30715960
|
G | A | 29 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0238others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.307-3872C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715960 | ||||||
| chr8:30715961
|
C | A | 1 | a0001c0001t0002g0201 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.307-3873G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715961 | ||||||
| chr8:30715967
|
T | A | 1 | a0001c0001t0004g0081 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.307-3879A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715967 | ||||||
| chr8:30716230
|
C | A | 48 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(45): Show | 48 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.307-4142G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716230 | ||||||
| chr8:30716491
|
C | A | 10 | a0001c0001t0005g0249a0001c0001t0005g0278a0001c0001t0005g0279others(7): Show | 10 | HG02280.hp1 HG02572.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-4403G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716491 | ||||||
| chr8:30716668
|
T | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.307-4580A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716668 | ||||||
| chr8:30716744
|
C | G | 1 | a0001c0001t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.307-4656G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716744 | ||||||
| chr8:30716806
|
C | A | 1 | a0003c0006t0008g0345 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-4718G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716806 | ||||||
| chr8:30716814
|
A | C | 1 | a0001c0001t0004g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.307-4726T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716814 | ||||||
| chr8:30716819
|
T | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.307-4731A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716819 | ||||||
| chr8:30716914
|
C | A | 2 | a0001c0001t0020g0168a0001c0001t0020g0169 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.307-4826G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716914 | ||||||
| chr8:30716916
|
A | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.307-4828T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716916 | ||||||
| chr8:30716952
|
C | T | 1 | a0001c0001t0006g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.307-4864G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716952 | ||||||
| chr8:30716973
|
T | C | 3 | a0001c0001t0005g0203a0001c0004t0045g0330a0005c0008t0037g0204 | 3 | HG02630.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.307-4885A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716973 | ||||||
| chr8:30717042
|
A | G | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307-4954T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717042 | ||||||
| chr8:30717119
|
C | A | 1 | a0001c0001t0002g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.307-5031G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717119 | ||||||
| chr8:30717152
|
G | A | 25 | a0001c0001t0003g0218a0001c0001t0012g0216a0001c0001t0018g0215others(22): Show | 25 | HG00621.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.307-5064C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717152 | ||||||
| chr8:30717232
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(205): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.307-5144A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717232 | ||||||
| chr8:30717249
|
G | GAAACAAA others(1): Show |
342 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.307-5169_307-5162d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717249 | ||||||
| chr8:30717249
|
G | GAAACAAA others(5): Show |
3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0015g0172 | 3 | HG01071.hp2 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.307-5173_307-5162d others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717249 | ||||||
| chr8:30717369
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.307-5281C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717369 | ||||||
| chr8:30717423
|
G | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(242): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.307-5335C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717423 | ||||||
| chr8:30717468
|
G | A | 36 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(33): Show | 37 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.307-5380C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717468 | ||||||
| chr8:30717499
|
T | C | 3 | a0001c0001t0020g0168a0001c0001t0020g0169a0001c0001t0026g0167 | 3 | HG02055.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.307-5411A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717499 | ||||||
| chr8:30717543
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.307-5455A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717543 | ||||||
| chr8:30717762
|
CA | C | 32 | a0001c0001t0002g0316a0001c0001t0003g0218a0001c0001t0012g0216others(29): Show | 32 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.307-5675delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717762 | ||||||
| chr8:30717827
|
G | A | 4 | a0001c0003t0005g0008a0001c0003t0025g0009a0001c0003t0025g0010others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-5739C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717827 | ||||||
| chr8:30717866
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.307-5778G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717866 | ||||||
| chr8:30717872
|
G | A | 3 | a0001c0004t0006g0332a0002c0002t0001g0337a0002c0002t0023g0338 | 3 | HG02895.hp1 NA18906.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.307-5784C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717872 | ||||||
| chr8:30717892
|
G | A | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0170 | 3 | HG00099.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.307-5804C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717892 | ||||||
| chr8:30717909
|
G | C | 6 | a0001c0001t0003g0218a0001c0001t0012g0216a0001c0001t0018g0215others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-5821C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717909 | ||||||
| chr8:30717930
|
G | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01261.hp2 HG02602.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.307-5842C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717930 | ||||||
| chr8:30718089
|
G | T | 7 | a0001c0001t0002g0261a0001c0001t0003g0256a0001c0001t0003g0257others(4): Show | 7 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-6001C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718089 | ||||||
| chr8:30718111
|
A | AAAAT | 222 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(219): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.307-6027_307-6024d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718111 | ||||||
| chr8:30718111
|
A | AAAATAAA others(1): Show |
24 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0224others(21): Show | 25 | HG00099.hp1 HG00735.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.307-6031_307-6024d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718111 | ||||||
| chr8:30718111
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307-6035_307-6024d others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718111 | ||||||
| chr8:30718282
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.307-6194A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718282 | ||||||
| chr8:30718321
|
T | C | 36 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0001t0002g0261others(33): Show | 37 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.307-6233A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718321 | ||||||
| chr8:30718357
|
G | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.307-6269C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718357 | ||||||
| chr8:30718489
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307-6401G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718489 | ||||||
| chr8:30718696
|
C | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.307-6608G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718696 | ||||||
| chr8:30718775
|
A | T | 4 | a0001c0003t0005g0008a0001c0003t0025g0009a0001c0003t0025g0010others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-6687T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718775 | ||||||
| chr8:30718891
|
C | T | 1 | a0001c0001t0011g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.307-6803G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718891 | ||||||
| chr8:30718920
|
GT | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.307-6833delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718920 | ||||||
| chr8:30718926
|
T | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.307-6838A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718926 | ||||||
| chr8:30718999
|
G | A | 2 | a0001c0001t0029g0032a0001c0001t0032g0031 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.307-6911C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718999 | ||||||
| chr8:30719104
|
AT | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.307-7017delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719104 | ||||||
| chr8:30719104
|
ATT | A | 10 | a0001c0001t0003g0247a0001c0001t0003g0251a0001c0001t0014g0018others(7): Show | 10 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-7018_307-7017d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719104 | ||||||
| chr8:30719164
|
T | A | 19 | a0001c0004t0006g0332a0001c0004t0012g0323a0002c0002t0001g0324others(16): Show | 19 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.307-7076A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719164 | ||||||
| chr8:30719249
|
G | C | 2 | a0001c0004t0045g0330a0005c0008t0037g0204 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.307-7161C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719249 | ||||||
| chr8:30719273
|
AAT | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.307-7187_307-7186d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719273 | ||||||
| chr8:30719287
|
T | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.307-7199A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719287 | ||||||
| chr8:30719309
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.307-7221T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719309 | ||||||
| chr8:30719318
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.307-7230C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719318 | ||||||
| chr8:30719512
|
A | G | 2 | a0001c0001t0029g0032a0001c0001t0032g0031 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.307-7424T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719512 | ||||||
| chr8:30719572
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.307-7484A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719572 | ||||||
| chr8:30719679
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.307-7591G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719679 | ||||||
| chr8:30719683
|
G | T | 2 | a0001c0001t0005g0208a0001c0001t0007g0209 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.307-7595C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719683 | ||||||
| chr8:30719712
|
T | C | 1 | a0001c0001t0049g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.307-7624A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719712 | ||||||
| chr8:30719884
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.306+7646T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719884 | ||||||
| chr8:30719928
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.306+7602C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719928 | ||||||
| chr8:30719950
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+7580C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719950 | ||||||
| chr8:30720087
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.306+7443C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720087 | ||||||
| chr8:30720171
|
C | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.306+7359G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720171 | ||||||
| chr8:30720357
|
G | C | 3 | a0001c0001t0005g0203a0001c0004t0045g0330a0005c0008t0037g0204 | 3 | HG02630.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.306+7173C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720357 | ||||||
| chr8:30720389
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+7141A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720389 | ||||||
| chr8:30720477
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.306+7053T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720477 | ||||||
| chr8:30720657
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.306+6873T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720657 | ||||||
| chr8:30720671
|
G | GAA | 230 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(227): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.306+6857_306+6858d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720671 | ||||||
| chr8:30720765
|
A | G | 41 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(38): Show | 41 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+6765T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720765 | ||||||
| chr8:30720856
|
CACAGGT | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6668_306+6673d others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720856 | ||||||
| chr8:30720863
|
G | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6667C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720863 | ||||||
| chr8:30720934
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.306+6596C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720934 | ||||||
| chr8:30720939
|
C | T | 1 | a0001c0001t0010g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.306+6591G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720939 | ||||||
| chr8:30720949
|
C | A | 1 | a0003c0006t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.306+6581G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720949 | ||||||
| chr8:30720967
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6563G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720967 | ||||||
| chr8:30720969
|
G | A | 46 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(43): Show | 46 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.306+6561C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720969 | ||||||
| chr8:30721012
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6518A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721012 | ||||||
| chr8:30721064
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6466G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721064 | ||||||
| chr8:30721087
|
C | A | 39 | a0001c0001t0001g0244a0001c0001t0001g0252a0001c0001t0001g0270others(36): Show | 40 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.306+6443G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721087 | ||||||
| chr8:30721128
|
T | C | 1 | a0001c0001t0015g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.306+6402A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721128 | ||||||
| chr8:30721134
|
C | CTCTG | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6395_306+6396i others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721134 | ||||||
| chr8:30721143
|
G | A | 1 | a0006c0007t0001g0173 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.306+6387C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721143 | ||||||
| chr8:30721151
|
GAAGA | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6375_306+6378d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721151 | ||||||
| chr8:30721213
|
C | A | 1 | a0001c0001t0010g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.306+6317G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721213 | ||||||
| chr8:30721421
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+6109A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721421 | ||||||
| chr8:30721426
|
G | A | 3 | a0001c0001t0022g0205a0001c0001t0022g0211a0001c0003t0012g0012 | 3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.306+6104C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721426 | ||||||
| chr8:30721451
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.306+6079C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721451 | ||||||
| chr8:30721480
|
G | T | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+6050C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721480 | ||||||
| chr8:30721522
|
G | A | 1 | a0001c0001t0004g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.306+6008C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721522 | ||||||
| chr8:30721577
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.306+5953A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721577 | ||||||
| chr8:30721658
|
GA | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+5871delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721658 | ||||||
| chr8:30721693
|
T | A | 1 | a0003c0006t0018g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.306+5837A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721693 | ||||||
| chr8:30721717
|
T | C | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.306+5813A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721717 | ||||||
| chr8:30721768
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.306+5762G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721768 | ||||||
| chr8:30721800
|
C | T | 1 | a0002c0002t0019g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.306+5730G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721800 | ||||||
| chr8:30721850
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+5680C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721850 | ||||||
| chr8:30721875
|
G | A | 1 | a0001c0001t0003g0297 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.306+5655C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721875 | ||||||
| chr8:30721887
|
C | T | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+5643G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721887 | ||||||
| chr8:30721939
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+5591G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721939 | ||||||
| chr8:30721953
|
T | C | 1 | a0001c0001t0012g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+5577A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721953 | ||||||
| chr8:30721982
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+5548A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721982 | ||||||
| chr8:30722007
|
C | A | 1 | a0001c0001t0008g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.306+5523G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722007 | ||||||
| chr8:30722013
|
C | CA | 12 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0004g0229others(9): Show | 12 | HG02074.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.306+5516dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722013 | ||||||
| chr8:30722231
|
G | T | 47 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(44): Show | 47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+5299C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722231 | ||||||
| chr8:30722236
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+5294G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722236 | ||||||
| chr8:30722454
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0004g0013others(1): Show | 4 | HG00438.hp2 HG00597.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+5076C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722454 | ||||||
| chr8:30722518
|
G | GAGTTCGA others(7): Show |
232 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.306+4998_306+5011d others(16): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722518 | ||||||
| chr8:30722523
|
C | CGAGACCA others(7): Show |
2 | a0001c0001t0004g0078a0001c0001t0018g0077 | 2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.306+5006_306+5007i others(16): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722523 | ||||||
| chr8:30722589
|
A | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+4941T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722589 | ||||||
| chr8:30722596
|
T | C | 1 | a0001c0001t0004g0229 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.306+4934A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722596 | ||||||
| chr8:30722630
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+4900C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722630 | ||||||
| chr8:30722691
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.306+4839G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722691 | ||||||
| chr8:30722692
|
C | T | 47 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(44): Show | 47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+4838G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722692 | ||||||
| chr8:30722696
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+4834G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722696 | ||||||
| chr8:30722731
|
C | CAA | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+4797_306+4798d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | ||||||
| chr8:30722731
|
CA | C | 94 | a0001c0001t0002g0224a0001c0001t0002g0286a0001c0001t0002g0296others(91): Show | 94 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.306+4798delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | ||||||
| chr8:30722731
|
CAA | C | 8 | a0001c0004t0012g0323a0002c0002t0001g0324a0002c0002t0001g0325others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+4797_306+4798d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | ||||||
| chr8:30722731
|
CAAAAAAA others(1): Show |
C | 224 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.306+4791_306+4798d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | ||||||
| chr8:30722777
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+4753G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722777 | ||||||
| chr8:30722814
|
T | A | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+4716A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722814 | ||||||
| chr8:30722833
|
T | C | 2 | a0001c0003t0012g0011a0003c0006t0012g0342 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.306+4697A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722833 | ||||||
| chr8:30722998
|
T | A | 2 | a0001c0001t0005g0203a0005c0008t0037g0204 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.306+4532A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722998 | ||||||
| chr8:30723060
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.306+4470C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723060 | ||||||
| chr8:30723067
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.306+4463C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723067 | ||||||
| chr8:30723092
|
C | T | 2 | a0001c0001t0011g0180a0001c0001t0011g0181 | 2 | HG00558.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.306+4438G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723092 | ||||||
| chr8:30723190
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+4340C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723190 | ||||||
| chr8:30723309
|
T | C | 2 | a0001c0001t0011g0180a0001c0001t0011g0181 | 2 | HG00558.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.306+4221A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723309 | ||||||
| chr8:30723363
|
C | G | 20 | a0001c0004t0006g0332a0001c0004t0012g0323a0001c0004t0045g0330others(17): Show | 20 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.306+4167G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723363 | ||||||
| chr8:30723384
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.306+4146G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723384 | ||||||
| chr8:30723385
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.306+4145C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723385 | ||||||
| chr8:30723518
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.306+4012G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723518 | ||||||
| chr8:30723556
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+3974A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723556 | ||||||
| chr8:30723575
|
T | G | 1 | a0001c0001t0009g0183 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.306+3955A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723575 | ||||||
| chr8:30723578
|
G | T | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+3952C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723578 | ||||||
| chr8:30723588
|
C | T | 4 | a0001c0001t0002g0047a0001c0001t0007g0048a0001c0001t0007g0074others(1): Show | 4 | NA18944.hp1 NA19063.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+3942G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723588 | ||||||
| chr8:30723608
|
T | C | 1 | a0001c0001t0004g0184 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.306+3922A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723608 | ||||||
| chr8:30723643
|
T | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.306+3887A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723643 | ||||||
| chr8:30723783
|
A | AAC | 5 | a0001c0001t0003g0285a0001c0001t0005g0207a0001c0001t0011g0206others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+3745_306+3746d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | ||||||
| chr8:30723783
|
AAC | A | 50 | a0001c0001t0002g0286a0001c0001t0002g0296a0001c0001t0003g0218others(47): Show | 50 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.306+3745_306+3746d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | ||||||
| chr8:30723783
|
AACAC | A | 41 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0005g0203others(38): Show | 41 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+3743_306+3746d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | ||||||
| chr8:30723783
|
AACACACA others(1): Show |
A | 41 | a0001c0001t0001g0244a0001c0001t0001g0252a0001c0001t0001g0270others(38): Show | 42 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.306+3739_306+3746d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | ||||||
| chr8:30723783
|
AACACACA others(3): Show |
A | 193 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.306+3737_306+3746d others(12): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | ||||||
| chr8:30723818
|
A | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.306+3712T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723818 | ||||||
| chr8:30723826
|
C | T | 5 | a0001c0003t0005g0008a0001c0003t0015g0006a0001c0003t0025g0009others(2): Show | 5 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+3704G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723826 | ||||||
| chr8:30723841
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.306+3689T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723841 | ||||||
| chr8:30723883
|
C | T | 3 | a0001c0001t0004g0071a0001c0001t0004g0189a0001c0009t0001g0027 | 3 | NA18964.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.306+3647G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723883 | ||||||
| chr8:30723984
|
C | A | 47 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(44): Show | 47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+3546G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723984 | ||||||
| chr8:30724078
|
A | G | 47 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(44): Show | 47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+3452T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724078 | ||||||
| chr8:30724261
|
C | T | 47 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(44): Show | 47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+3269G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724261 | ||||||
| chr8:30724311
|
C | G | 1 | a0001c0004t0045g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.306+3219G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724311 | ||||||
| chr8:30724338
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.306+3192T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724338 | ||||||
| chr8:30724544
|
C | CT | 41 | a0001c0001t0001g0299a0001c0001t0003g0210a0001c0001t0004g0030others(38): Show | 41 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+2985dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | ||||||
| chr8:30724544
|
C | CTT | 80 | a0001c0001t0001g0252a0001c0001t0001g0270a0001c0001t0001g0301others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.306+2984_306+2985d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | ||||||
| chr8:30724544
|
C | CTTT | 191 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.306+2983_306+2985d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | ||||||
| chr8:30724544
|
C | CTTTT | 31 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0063others(28): Show | 31 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.306+2982_306+2985d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | ||||||
| chr8:30724694
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18944.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.306+2836G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724694 | ||||||
| chr8:30724724
|
C | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.306+2806G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724724 | ||||||
| chr8:30724787
|
T | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.306+2743A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724787 | ||||||
| chr8:30724788
|
G | T | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+2742C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724788 | ||||||
| chr8:30724794
|
C | T | 1 | a0003c0006t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.306+2736G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724794 | ||||||
| chr8:30724834
|
T | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.306+2696A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724834 | ||||||
| chr8:30724885
|
A | C | 7 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+2645T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724885 | ||||||
| chr8:30725015
|
T | G | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0011g0195 | 3 | NA18977.hp2 NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.306+2515A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725015 | ||||||
| chr8:30725106
|
T | G | 54 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(51): Show | 54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+2424A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725106 | ||||||
| chr8:30725137
|
C | T | 47 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(44): Show | 47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+2393G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725137 | ||||||
| chr8:30725307
|
C | T | 2 | a0001c0001t0012g0216a0001c0001t0018g0215 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.306+2223G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725307 | ||||||
| chr8:30725311
|
C | T | 1 | a0001c0001t0004g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.306+2219G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725311 | ||||||
| chr8:30725351
|
T | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.306+2179A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725351 | ||||||
| chr8:30725375
|
G | A | 20 | a0001c0004t0006g0332a0001c0004t0012g0323a0001c0004t0045g0330others(17): Show | 20 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.306+2155C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725375 | ||||||
| chr8:30725410
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.306+2120T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725410 | ||||||
| chr8:30725414
|
G | A | 54 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(51): Show | 54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+2116C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725414 | ||||||
| chr8:30725491
|
C | T | 54 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(51): Show | 54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+2039G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725491 | ||||||
| chr8:30725519
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.306+2011G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725519 | ||||||
| chr8:30725559
|
C | T | 8 | a0001c0004t0012g0323a0002c0002t0001g0324a0002c0002t0001g0325others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+1971G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725559 | ||||||
| chr8:30725580
|
C | A | 54 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(51): Show | 54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+1950G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725580 | ||||||
| chr8:30725881
|
C | CA | 30 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0301others(27): Show | 30 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.306+1648dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | ||||||
| chr8:30725881
|
C | CAA | 39 | a0001c0001t0002g0224a0001c0001t0003g0218a0001c0001t0003g0223others(36): Show | 39 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.306+1647_306+1648d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | ||||||
| chr8:30725881
|
C | CAAA | 7 | a0001c0001t0007g0225a0001c0003t0012g0011a0001c0003t0015g0006others(4): Show | 7 | HG00621.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+1646_306+1648d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | ||||||
| chr8:30725881
|
CA | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0008g0235others(4): Show | 7 | HG00408.hp2 HG01515.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+1648delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | ||||||
| chr8:30725888
|
A | C | 1 | a0001c0009t0001g0027 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.306+1642T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725888 | ||||||
| chr8:30725918
|
G | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.306+1612C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725918 | ||||||
| chr8:30726064
|
C | T | 45 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(42): Show | 45 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.306+1466G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726064 | ||||||
| chr8:30726186
|
C | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.306+1344G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726186 | ||||||
| chr8:30726197
|
A | G | 51 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(48): Show | 51 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.306+1333T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726197 | ||||||
| chr8:30726249
|
G | A | 45 | a0001c0001t0002g0224a0001c0001t0002g0316a0001c0001t0003g0218others(42): Show | 45 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.306+1281C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726249 | ||||||
| chr8:30726292
|
G | T | 6 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+1238C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726292 | ||||||
| chr8:30726387
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0004g0024a0001c0001t0004g0025others(1): Show | 4 | HG01071.hp1 HG01081.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+1143G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726387 | ||||||
| chr8:30726429
|
T | C | 1 | a0005c0008t0037g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.306+1101A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726429 | ||||||
| chr8:30726471
|
T | C | 15 | a0001c0001t0003g0210a0001c0001t0005g0207a0001c0001t0005g0208others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.306+1059A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726471 | ||||||
| chr8:30726547
|
C | T | 6 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+983G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726547 | ||||||
| chr8:30726554
|
G | T | 45 | a0001c0001t0002g0224a0001c0001t0003g0218a0001c0001t0003g0223others(42): Show | 45 | HG00621.hp2 HG01891.hp2 HG02055.hp2 others(42): Show |
intron_variant | MODIFIER | c.306+976C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726554 | ||||||
| chr8:30726601
|
A | C | 1 | a0002c0010t0015g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.306+929T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726601 | ||||||
| chr8:30726632
|
G | A | 9 | a0001c0001t0002g0224a0001c0001t0003g0218a0001c0001t0003g0223others(6): Show | 9 | HG02280.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.306+898C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726632 | ||||||
| chr8:30726661
|
C | A | 1 | a0001c0003t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+869G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726661 | ||||||
| chr8:30726713
|
G | C | 4 | a0001c0001t0001g0228a0001c0001t0003g0227a0001c0001t0004g0226others(1): Show | 4 | HG02074.hp1 HG02155.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+817C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726713 | ||||||
| chr8:30726991
|
A | C | 1 | a0001c0003t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+539T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726991 | ||||||
| chr8:30727137
|
T | C | 36 | a0001c0001t0006g0230a0001c0001t0039g0231a0001c0003t0005g0008others(33): Show | 36 | HG00621.hp2 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.306+393A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727137 | ||||||
| chr8:30727237
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0004g0013 | 3 | HG00438.hp2 HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.306+293G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727237 | ||||||
| chr8:30727300
|
C | T | 1 | a0001c0001t0004g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.306+230G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727300 | ||||||
| chr8:30727301
|
C | A | 1 | a0001c0001t0004g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.306+229G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727301 | ||||||
| chr8:30727332
|
G | C | 2 | a0001c0001t0004g0233a0004c0005t0010g0005 | 2 | HG00738.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.306+198C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727332 | ||||||
| chr8:30727362
|
T | C | 7 | a0001c0001t0002g0316a0001c0001t0004g0314a0001c0001t0005g0315others(4): Show | 7 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+168A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727362 | ||||||
| chr8:30727365
|
C | T | 34 | a0001c0003t0005g0008a0001c0003t0012g0011a0001c0003t0012g0012others(31): Show | 34 | HG00621.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.306+165G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727365 | ||||||
| chr8:30727406
|
G | A | 90 | a0001c0001t0001g0244a0001c0001t0001g0252a0001c0001t0001g0270others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.306+124C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727406 | ||||||
| chr8:30727427
|
C | G | 34 | a0001c0003t0005g0008a0001c0003t0012g0011a0001c0003t0012g0012others(31): Show | 34 | HG00621.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.306+103G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727427 | ||||||
| chr8:30727483
|
C | A | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18966.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.306+47G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727483 |