| geneid | 9489 |
|---|---|
| ensemblid | ENSG00000087157.19 |
| hgncid | 30029 |
| symbol | PGS1 |
| name | phosphatidylglycerophosphate synthase 1 |
| refseq_nuc | NM_024419.5 |
| refseq_prot | NP_077733.3 |
| ensembl_nuc | ENST00000262764.11 |
| ensembl_prot | ENSP00000262764.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 78378649 |
| end | 78424659 |
| strand | + |
| ver | v1.2 |
| region | chr17:78378649-78424659 |
| region5000 | chr17:78373649-78429659 |
| regionname0 | PGS1_chr17_78378649_78424659 |
| regionname5000 | PGS1_chr17_78373649_78429659 |
| 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 | 556 | 389 | 87 | 76 | 164 | 16 | 44 | 127 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0002 | 0/0 | 556 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0003 | 0/0 | 556 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0004 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1671 | 198 | 44 | 36 | 80 | 11 | 27 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0002 | 1/1 | 1671 | 168 | 28 | 36 | 80 | 5 | 17 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0003 | 0/0 | 1671 | 15 | 13 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0004 | 0/0 | 1671 | 5 | 5 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0005 | 0/0 | 1671 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0006 | 0/0 | 1671 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0007 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0008 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0009 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0010 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0011 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0012 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| c0013 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 627 | 325 | 61 | 58 | 156 | 10 | 39 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0002 | 0/0 | 631 | 44 | 19 | 12 | 3 | 6 | 4 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0003 | 1/0 | 627 | 7 | 6 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0004 | 0/0 | 624 | 5 | 0 | 0 | 5 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0005 | 0/0 | 627 | 3 | 2 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0006 | 0/0 | 627 | 2 | 0 | 1 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0007 | 0/0 | 627 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0008 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0009 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0010 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0011 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0012 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0013 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0014 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0015 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| t0016 | 0/0 | 631 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| 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 | 4 | 0 | 4 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0003 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1671 | 198 | 44 | 36 | 80 | 11 | 27 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002 | 1/1 | 1671 | 168 | 28 | 36 | 80 | 5 | 17 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0003 | 0/0 | 1671 | 15 | 13 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0006 | 0/0 | 1671 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0007 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0008 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0010 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0011 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0012 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0013 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0002c0004 | 0/0 | 1671 | 5 | 5 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0003c0005 | 0/0 | 1671 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0004c0009 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2297 | 177 | 36 | 33 | 75 | 7 | 26 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0002 | 0/0 | 2301 | 10 | 3 | 3 | 0 | 4 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0003 | 0/0 | 2297 | 3 | 3 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0004 | 0/0 | 2294 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0005 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0006 | 0/0 | 2297 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0009 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0010 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0012 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0001t0015 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0001 | 0/1 | 2297 | 135 | 19 | 25 | 74 | 3 | 13 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0002 | 0/0 | 2301 | 21 | 5 | 7 | 3 | 2 | 4 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0003 | 1/0 | 2297 | 4 | 3 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0004 | 0/0 | 2294 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0005 | 0/0 | 2297 | 2 | 1 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0007 | 0/0 | 2297 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0002t0013 | 0/0 | 2297 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0003t0001 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0003t0002 | 0/0 | 2301 | 12 | 11 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0003t0008 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0003t0016 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0006t0001 | 0/0 | 2297 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0007t0006 | 0/0 | 2297 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0008t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0010t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0011t0002 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0012t0008 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0001c0013t0011 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0002c0004t0001 | 0/0 | 2297 | 5 | 5 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0003c0005t0001 | 0/0 | 2297 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| a0004c0009t0014 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | copy fasta | chr17 | 78373649 | 78429659 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0009g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0010g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0015g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0016g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0007t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0010t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0011t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0012t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0013t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0003c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0003c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0003c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0004c0009t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0164 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0166 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | FIN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0155 | EUR | FIN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00423 | hp2 | a0001 | c0010 | t0001 | g0227 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00741 | hp1 | a0001 | c0007 | t0006 | g0170 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0371 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01106 | hp1 | a0001 | c0003 | t0016 | g0074 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01109 | hp1 | a0001 | c0002 | t0007 | g0015 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01169 | hp2 | a0001 | c0002 | t0013 | g0001 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0082 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01256 | hp1 | a0001 | c0011 | t0002 | g0315 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0370 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0191 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01952 | hp1 | a0001 | c0002 | t0007 | g0110 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0372 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02040 | hp2 | a0004 | c0009 | t0014 | g0145 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0184 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0173 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CDX | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0377 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0075 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0194 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02647 | hp2 | a0001 | c0013 | t0011 | g0187 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0079 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0085 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0183 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02886 | hp2 | a0001 | c0003 | t0008 | g0016 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0342 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0181 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0182 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0179 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0178 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0185 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0177 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0193 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0097 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0195 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03579 | hp1 | a0001 | c0012 | t0008 | g0188 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0365 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0224 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0364 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0291 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0209 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18939 | hp1 | a0001 | c0001 | t0010 | g0352 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18940 | hp1 | a0001 | c0006 | t0001 | g0295 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0138 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18964 | hp1 | a0003 | c0005 | t0001 | g0135 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18971 | hp2 | a0001 | c0008 | t0001 | g0008 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18980 | hp1 | a0003 | c0005 | t0001 | g0129 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18995 | hp2 | a0001 | c0001 | t0015 | g0300 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19000 | hp2 | a0003 | c0005 | t0001 | g0137 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19001 | hp2 | a0001 | c0001 | t0009 | g0368 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19012 | hp1 | a0001 | c0002 | t0004 | g0124 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19057 | hp2 | a0001 | c0006 | t0001 | g0261 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0190 | AFR | ASW | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ASW | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0065 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0203 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | GIH | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0024 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0087 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0176 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0180 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0027 | REF | REF | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0086 | REF | REF | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78403688
|
A | T | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1001A>T | p.Gln334Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1018/2297 | 1001/1671 | 334/556 | chr17 | 78403688 | ||
| chr17:78404024
|
T | G | 1 | a0002 | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
missense_variant | MODERATE | c.1337T>G | p.Leu446Arg | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1354/2297 | 1337/1671 | 446/556 | chr17 | 78404024 | ||
| chr17:78414896
|
G | T | 1 | a0003 | 3 | NA18964.hp1 NA18980.hp1 NA19000.hp2 |
missense_variant | MODERATE | c.1420G>T | p.Ala474Ser | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/10 | 1437/2297 | 1420/1671 | 474/556 | chr17 | 78414896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78378756
|
C | T | 2 | a0001c0012a0001c0013 | 2 | HG02647.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.91C>T | p.Leu31Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/10 | 108/2297 | 91/1671 | 31/556 | chr17 | 78378756 | ||
| chr17:78399349
|
C | T | 6 | a0001c0001a0001c0003a0001c0006others(3): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
splice_region_variant&synonymous_variant | LOW | c.513C>T | p.Gly171Gly | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/10 | 530/2297 | 513/1671 | 171/556 | chr17 | 78399349 | ||
| chr17:78399427
|
G | A | 1 | a0001c0007 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.591G>A | p.Thr197Thr | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/10 | 608/2297 | 591/1671 | 197/556 | chr17 | 78399427 | ||
| chr17:78400764
|
G | A | 1 | a0001c0010 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.789G>A | p.Thr263Thr | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/10 | 806/2297 | 789/1671 | 263/556 | chr17 | 78400764 | ||
| chr17:78403746
|
G | A | 1 | a0001c0003 | 15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
synonymous_variant | LOW | c.1059G>A | p.Pro353Pro | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1076/2297 | 1059/1671 | 353/556 | chr17 | 78403746 | ||
| chr17:78404082
|
C | T | 1 | a0001c0011 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1395C>T | p.His465His | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1412/2297 | 1395/1671 | 465/556 | chr17 | 78404082 | ||
| chr17:78419621
|
C | T | 1 | a0001c0006 | 2 | NA18940.hp1 NA19057.hp2 |
synonymous_variant | LOW | c.1627C>T | p.Leu543Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/10 | 1644/2297 | 1627/1671 | 543/556 | chr17 | 78419621 | ||
| chr17:78419647
|
G | C | 1 | a0001c0008 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1653G>C | p.Leu551Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/10 | 1670/2297 | 1653/1671 | 551/556 | chr17 | 78419647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78424112
|
G | A | 2 | a0001c0001t0009a0001c0001t0010 | 2 | NA18939.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4447 | chr17 | 78424112 | |||||
| chr17:78424137
|
G | A | 1 | a0001c0013t0011 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4472 | chr17 | 78424137 | |||||
| chr17:78424292
|
G | A | 24 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(21): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*242G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4627 | chr17 | 78424292 | |||||
| chr17:78424307
|
C | A | 2 | a0001c0001t0006a0001c0007t0006 | 2 | HG00741.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*257C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4642 | chr17 | 78424307 | |||||
| chr17:78424312
|
G | A | 5 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(2): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*262G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4647 | chr17 | 78424312 | |||||
| chr17:78424356
|
T | A | 5 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(2): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*306T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4691 | chr17 | 78424356 | |||||
| chr17:78424410
|
T | TTTTCAGA others(90): Show |
1 | a0004c0009t0014 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*362_*458dupTTCAGA others(91): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4844 | INFO_REALIGN_3_PRIME | chr17 | 78424410 | ||||
| chr17:78424414
|
C | T | 2 | a0001c0003t0008a0001c0012t0008 | 2 | HG02886.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*364C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4749 | chr17 | 78424414 | |||||
| chr17:78424432
|
C | T | 1 | a0001c0002t0007 | 2 | HG01109.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*382C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4767 | chr17 | 78424432 | |||||
| chr17:78424436
|
A | G | 1 | a0001c0001t0015 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*386A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4771 | chr17 | 78424436 | |||||
| chr17:78424502
|
G | A | 2 | a0001c0001t0005a0001c0002t0005 | 3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*452G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4837 | chr17 | 78424502 | |||||
| chr17:78424525
|
C | A | 1 | a0001c0001t0009 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4860 | chr17 | 78424525 | |||||
| chr17:78424526
|
A | G | 1 | a0001c0002t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4861 | chr17 | 78424526 | |||||
| chr17:78424561
|
A | ATTAT | 5 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(2): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*513_*514insATTT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4899 | INFO_REALIGN_3_PRIME | chr17 | 78424561 | ||||
| chr17:78424582
|
A | G | 1 | a0001c0003t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4917 | chr17 | 78424582 | |||||
| chr17:78424610
|
GTTT | G | 2 | a0001c0001t0004a0001c0002t0004 | 5 | HG02040.hp1 HG02129.hp1 NA18948.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*563_*565delTTT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4948 | INFO_REALIGN_3_PRIME | chr17 | 78424610 | ||||
| chr17:78424617
|
T | G | 1 | a0001c0001t0012 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*567T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4952 | chr17 | 78424617 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78378882
|
C | T | 1 | a0001c0001t0001g0377 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143+74C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78378882 | ||||||
| chr17:78378897
|
C | G | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.143+89C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78378897 | ||||||
| chr17:78379014
|
A | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(124): Show | 137 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.143+206A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379014 | ||||||
| chr17:78379049
|
C | G | 1 | a0001c0002t0001g0329 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.143+241C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379049 | ||||||
| chr17:78379266
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.143+458G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379266 | ||||||
| chr17:78379271
|
T | C | 1 | a0001c0002t0007g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.143+463T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379271 | ||||||
| chr17:78379445
|
G | A | 1 | a0001c0003t0008g0016 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.143+637G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379445 | ||||||
| chr17:78379657
|
C | T | 1 | a0001c0001t0001g0376 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143+849C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379657 | ||||||
| chr17:78379842
|
T | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(3): Show | 6 | NA18612.hp1 NA18941.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+1034T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379842 | ||||||
| chr17:78379875
|
C | CT | 47 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0333others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.143+1077dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78379875 | |||||
| chr17:78379976
|
C | T | 3 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326 | 3 | HG02148.hp1 NA18966.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.143+1168C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379976 | ||||||
| chr17:78380027
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143+1219C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380027 | ||||||
| chr17:78380155
|
C | T | 20 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(17): Show | 20 | HG00558.hp2 HG01069.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.143+1347C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380155 | ||||||
| chr17:78380173
|
G | T | 1 | a0001c0002t0002g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.143+1365G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380173 | ||||||
| chr17:78380230
|
C | T | 3 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0001t0001g0375 | 3 | NA18984.hp1 NA18990.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.143+1422C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380230 | ||||||
| chr17:78380270
|
A | G | 22 | a0001c0002t0001g0186a0001c0002t0001g0192a0001c0002t0002g0189others(19): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.143+1462A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380270 | ||||||
| chr17:78380444
|
T | C | 49 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0333others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+1636T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380444 | ||||||
| chr17:78380468
|
T | C | 1 | a0001c0002t0001g0023 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+1660T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380468 | ||||||
| chr17:78380576
|
C | A | 22 | a0001c0002t0001g0186a0001c0002t0001g0192a0001c0002t0002g0189others(19): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.143+1768C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380576 | ||||||
| chr17:78380637
|
AT | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG01891.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.143+1832delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78380637 | |||||
| chr17:78380728
|
A | G | 1 | a0001c0002t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.143+1920A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380728 | ||||||
| chr17:78380861
|
T | C | 1 | a0001c0003t0002g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.143+2053T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380861 | ||||||
| chr17:78380937
|
G | A | 1 | a0001c0002t0001g0025 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.143+2129G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380937 | ||||||
| chr17:78381020
|
A | G | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.143+2212A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381020 | ||||||
| chr17:78381082
|
A | T | 8 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(5): Show | 8 | HG00738.hp2 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.143+2274A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381082 | ||||||
| chr17:78381344
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.143+2536G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381344 | ||||||
| chr17:78381377
|
A | G | 140 | a0001c0001t0001g0152a0001c0001t0001g0327a0001c0001t0001g0328others(137): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.143+2569A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381377 | ||||||
| chr17:78381401
|
T | G | 225 | a0001c0001t0001g0067a0001c0001t0001g0152a0001c0001t0001g0327others(222): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.143+2593T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381401 | ||||||
| chr17:78381408
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.143+2600G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381408 | ||||||
| chr17:78381416
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.143+2608T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381416 | ||||||
| chr17:78381421
|
G | T | 1 | a0001c0011t0002g0315 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.143+2613G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381421 | ||||||
| chr17:78381476
|
C | T | 2 | a0001c0001t0001g0333a0001c0001t0001g0334 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.143+2668C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381476 | ||||||
| chr17:78381586
|
A | T | 1 | a0002c0004t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143+2778A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381586 | ||||||
| chr17:78381592
|
C | T | 44 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0335others(41): Show | 44 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.143+2784C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381592 | ||||||
| chr17:78381821
|
T | C | 1 | a0001c0002t0001g0111 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143+3013T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381821 | ||||||
| chr17:78381920
|
G | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG01891.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.143+3112G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381920 | ||||||
| chr17:78381921
|
C | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG00741.hp2 NA18983.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.143+3113C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381921 | ||||||
| chr17:78381966
|
C | A | 11 | a0001c0003t0002g0176a0001c0003t0002g0177a0001c0003t0002g0178others(8): Show | 11 | HG02055.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.143+3158C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381966 | ||||||
| chr17:78382009
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.143+3201G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382009 | ||||||
| chr17:78382014
|
A | G | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+3206A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382014 | ||||||
| chr17:78382117
|
A | G | 10 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+3309A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382117 | ||||||
| chr17:78382198
|
A | G | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.143+3390A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382198 | ||||||
| chr17:78382213
|
C | G | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+3405C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382213 | ||||||
| chr17:78382332
|
G | A | 47 | a0001c0001t0001g0152a0001c0002t0001g0007a0001c0002t0001g0008others(44): Show | 49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+3524G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382332 | ||||||
| chr17:78382339
|
C | T | 2 | a0001c0012t0008g0188a0001c0013t0011g0187 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.143+3531C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382339 | ||||||
| chr17:78382521
|
G | C | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.143+3713G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382521 | ||||||
| chr17:78382522
|
G | A | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+3714G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382522 | ||||||
| chr17:78382581
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.143+3773A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382581 | ||||||
| chr17:78382621
|
C | T | 4 | a0001c0001t0001g0369a0001c0001t0002g0370a0001c0001t0002g0371others(1): Show | 4 | HG01074.hp2 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+3813C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382621 | ||||||
| chr17:78382636
|
G | GT | 95 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0067others(92): Show | 99 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.143+3852dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | |||||
| chr17:78382636
|
G | GTT | 74 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(71): Show | 75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.143+3851_143+3852d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | |||||
| chr17:78382636
|
G | GTTT | 18 | a0001c0001t0001g0152a0001c0001t0001g0313a0001c0002t0001g0009others(15): Show | 19 | HG00673.hp1 HG01358.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.143+3850_143+3852d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | |||||
| chr17:78382636
|
G | T | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.143+3828G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382636 | ||||||
| chr17:78382636
|
GT | G | 26 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0314others(23): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.143+3852delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | |||||
| chr17:78382640
|
T | G | 2 | a0001c0001t0001g0223a0001c0001t0006g0224 | 2 | HG00733.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.143+3832T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382640 | ||||||
| chr17:78382642
|
T | TG | 33 | a0001c0002t0001g0004a0001c0002t0001g0025a0001c0002t0001g0026others(30): Show | 35 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.143+3834_143+3835i others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382642 | ||||||
| chr17:78382703
|
C | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG00544.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.143+3895C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382703 | ||||||
| chr17:78382728
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.143+3920C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382728 | ||||||
| chr17:78382745
|
C | G | 1 | a0001c0002t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143+3937C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382745 | ||||||
| chr17:78382788
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(121): Show | 134 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.143+3980G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382788 | ||||||
| chr17:78382836
|
G | A | 104 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0088others(101): Show | 108 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.143+4028G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382836 | ||||||
| chr17:78382902
|
C | T | 1 | a0001c0002t0002g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.143+4094C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382902 | ||||||
| chr17:78382934
|
C | T | 73 | a0001c0001t0001g0152a0001c0002t0001g0001a0001c0002t0001g0007others(70): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.143+4126C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382934 | ||||||
| chr17:78383179
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143+4371G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383179 | ||||||
| chr17:78383251
|
CT | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(123): Show | 136 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.143+4456delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78383251 | |||||
| chr17:78383336
|
C | A | 1 | a0001c0001t0001g0309 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.143+4528C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383336 | ||||||
| chr17:78383469
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.143+4661G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383469 | ||||||
| chr17:78383632
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.143+4824A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383632 | ||||||
| chr17:78383682
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.143+4874G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383682 | ||||||
| chr17:78383698
|
A | G | 1 | a0001c0002t0002g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143+4890A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383698 | ||||||
| chr17:78383788
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.143+4980C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383788 | ||||||
| chr17:78383857
|
G | A | 9 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0336others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.143+5049G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383857 | ||||||
| chr17:78383938
|
C | G | 11 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(8): Show | 11 | HG02738.hp1 NA18960.hp1 NA18989.hp1 others(8): Show |
intron_variant | MODIFIER | c.143+5130C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383938 | ||||||
| chr17:78383968
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.143+5160A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383968 | ||||||
| chr17:78383970
|
C | T | 2 | a0001c0012t0008g0188a0001c0013t0011g0187 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.143+5162C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383970 | ||||||
| chr17:78384045
|
G | A | 47 | a0001c0002t0001g0004a0001c0002t0001g0023a0001c0002t0001g0025others(44): Show | 49 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.143+5237G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384045 | ||||||
| chr17:78384161
|
G | A | 2 | a0001c0002t0001g0197a0001c0002t0001g0198 | 2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.143+5353G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384161 | ||||||
| chr17:78384321
|
C | T | 1 | a0001c0002t0001g0053 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.143+5513C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384321 | ||||||
| chr17:78384656
|
G | C | 1 | a0001c0001t0001g0344 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+5848G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384656 | ||||||
| chr17:78384656
|
G | T | 1 | a0001c0001t0001g0305 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.143+5848G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384656 | ||||||
| chr17:78384713
|
C | T | 1 | a0001c0002t0001g0066 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.143+5905C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384713 | ||||||
| chr17:78384765
|
C | A | 1 | a0001c0002t0001g0156 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.143+5957C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384765 | ||||||
| chr17:78384861
|
G | A | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+6053G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384861 | ||||||
| chr17:78384940
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(121): Show | 134 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.143+6132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384940 | ||||||
| chr17:78384969
|
G | A | 2 | a0001c0002t0001g0114a0001c0002t0001g0143 | 2 | NA19004.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.143+6161G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384969 | ||||||
| chr17:78385041
|
C | T | 33 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(30): Show | 33 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.143+6233C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385041 | ||||||
| chr17:78385180
|
G | A | 49 | a0001c0001t0001g0152a0001c0002t0001g0007a0001c0002t0001g0008others(46): Show | 51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.143+6372G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385180 | ||||||
| chr17:78385237
|
A | G | 49 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0333others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+6429A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385237 | ||||||
| chr17:78385278
|
C | T | 1 | a0001c0002t0002g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.143+6470C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385278 | ||||||
| chr17:78385293
|
A | AT | 31 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(28): Show | 31 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.143+6498dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78385293 | |||||
| chr17:78385322
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.143+6514A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385322 | ||||||
| chr17:78385335
|
T | C | 49 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0333others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+6527T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385335 | ||||||
| chr17:78385382
|
G | A | 84 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(81): Show | 87 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.143+6574G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385382 | ||||||
| chr17:78385413
|
C | T | 1 | a0001c0002t0002g0210 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.143+6605C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385413 | ||||||
| chr17:78385414
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.143+6606G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385414 | ||||||
| chr17:78385524
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.143+6716C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385524 | ||||||
| chr17:78385560
|
A | T | 1 | a0001c0001t0001g0362 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.143+6752A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385560 | ||||||
| chr17:78385576
|
G | C | 4 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0341others(1): Show | 4 | HG01884.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+6768G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385576 | ||||||
| chr17:78385662
|
A | C | 49 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0333others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.144-6814A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385662 | ||||||
| chr17:78385916
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144-6560C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385916 | ||||||
| chr17:78385998
|
C | T | 208 | a0001c0001t0001g0152a0001c0001t0001g0327a0001c0001t0001g0328others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.144-6478C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385998 | ||||||
| chr17:78386097
|
A | G | 1 | a0001c0001t0001g0376 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144-6379A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386097 | ||||||
| chr17:78386098
|
C | T | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-6378C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386098 | ||||||
| chr17:78386125
|
C | A | 9 | a0001c0002t0001g0186a0001c0002t0001g0192a0001c0002t0002g0189others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-6351C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386125 | ||||||
| chr17:78386179
|
G | A | 1 | a0001c0010t0001g0227 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.144-6297G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386179 | ||||||
| chr17:78386215
|
A | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(62): Show | 68 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.144-6261A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386215 | ||||||
| chr17:78386283
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.144-6193G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386283 | ||||||
| chr17:78386380
|
A | G | 1 | a0001c0003t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144-6096A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386380 | ||||||
| chr17:78386676
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-5800A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386676 | ||||||
| chr17:78386710
|
C | T | 157 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(154): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.144-5766C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386710 | ||||||
| chr17:78386869
|
C | A | 16 | a0001c0002t0001g0001a0001c0002t0001g0111a0001c0002t0001g0155others(13): Show | 18 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-5607C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386869 | ||||||
| chr17:78386972
|
A | G | 6 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(3): Show | 6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-5504A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386972 | ||||||
| chr17:78386972
|
ATGATGAT others(2): Show |
A | 32 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(29): Show | 32 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.144-5486_144-5478d others(11): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386972 | |||||
| chr17:78386975
|
ATGATGG | A | 6 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-5495_144-5490d others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386975 | |||||
| chr17:78386978
|
ATGG | A | 3 | a0001c0001t0001g0343a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG02486.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.144-5495_144-5493d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386978 | |||||
| chr17:78386978
|
ATGGTGAT others(5): Show |
A | 6 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0376others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-5495_144-5484d others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386978 | |||||
| chr17:78386990
|
G | A | 41 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.144-5486G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386990 | ||||||
| chr17:78387005
|
A | G | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-5471A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387005 | ||||||
| chr17:78387008
|
G | A | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-5468G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387008 | ||||||
| chr17:78387043
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.144-5433C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387043 | ||||||
| chr17:78387232
|
G | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG01891.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.144-5244G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387232 | ||||||
| chr17:78387238
|
A | G | 46 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(43): Show | 46 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.144-5238A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387238 | ||||||
| chr17:78387252
|
T | C | 46 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(43): Show | 46 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.144-5224T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387252 | ||||||
| chr17:78387257
|
G | A | 1 | a0001c0003t0002g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.144-5219G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387257 | ||||||
| chr17:78387291
|
A | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0270a0001c0001t0002g0304 | 4 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-5185A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387291 | ||||||
| chr17:78387294
|
G | C | 6 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-5182G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387294 | ||||||
| chr17:78387297
|
C | T | 1 | a0001c0001t0002g0014 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.144-5179C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387297 | ||||||
| chr17:78387303
|
C | CT | 9 | a0001c0001t0009g0368a0001c0002t0001g0069a0001c0002t0001g0070others(6): Show | 9 | HG01106.hp1 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-5161dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387303 | |||||
| chr17:78387303
|
C | CTT | 25 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0088others(22): Show | 26 | HG01243.hp1 HG02129.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.144-5162_144-5161d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387303 | |||||
| chr17:78387428
|
TAGCTGGG | T | 48 | a0001c0001t0001g0217a0001c0001t0001g0333a0001c0001t0001g0334others(45): Show | 48 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.144-5046_144-5040d others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387428 | |||||
| chr17:78387526
|
T | C | 12 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.144-4950T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387526 | ||||||
| chr17:78387540
|
A | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0294 | 3 | HG02602.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.144-4936A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387540 | ||||||
| chr17:78387550
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.144-4926T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387550 | ||||||
| chr17:78387590
|
C | T | 138 | a0001c0001t0001g0250a0001c0001t0001g0293a0001c0001t0001g0333others(135): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.144-4886C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387590 | ||||||
| chr17:78387598
|
C | CT | 108 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0088others(105): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.144-4859dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387598 | |||||
| chr17:78387598
|
C | CTT | 6 | a0001c0001t0001g0107a0001c0002t0001g0025a0001c0002t0001g0143others(3): Show | 6 | HG00741.hp1 HG02015.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-4860_144-4859d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387598 | |||||
| chr17:78387598
|
CT | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(177): Show | 192 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.144-4859delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387598 | |||||
| chr17:78387631
|
G | A | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-4845G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387631 | ||||||
| chr17:78387685
|
G | A | 351 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(348): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.144-4791G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387685 | ||||||
| chr17:78387726
|
G | A | 11 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0340others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-4750G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387726 | ||||||
| chr17:78387751
|
C | T | 3 | a0001c0001t0001g0348a0001c0001t0001g0376a0001c0001t0005g0342 | 3 | HG02818.hp1 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.144-4725C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387751 | ||||||
| chr17:78388052
|
T | C | 1 | a0001c0001t0003g0341 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.144-4424T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388052 | ||||||
| chr17:78388135
|
G | A | 1 | a0001c0001t0002g0345 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144-4341G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388135 | ||||||
| chr17:78388139
|
G | A | 46 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(43): Show | 46 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.144-4337G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388139 | ||||||
| chr17:78388173
|
G | A | 1 | a0001c0003t0002g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.144-4303G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388173 | ||||||
| chr17:78388195
|
G | A | 14 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(11): Show | 14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-4281G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388195 | ||||||
| chr17:78388197
|
G | C | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4279G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388197 | ||||||
| chr17:78388234
|
T | C | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4242T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388234 | ||||||
| chr17:78388258
|
C | T | 2 | a0001c0002t0001g0160a0001c0002t0001g0161 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.144-4218C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388258 | ||||||
| chr17:78388357
|
C | T | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4119C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388357 | ||||||
| chr17:78388436
|
G | T | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.144-4040G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388436 | ||||||
| chr17:78388452
|
A | G | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4024A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388452 | ||||||
| chr17:78388453
|
T | C | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4023T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388453 | ||||||
| chr17:78388456
|
C | T | 1 | a0001c0002t0001g0051 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.144-4020C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388456 | ||||||
| chr17:78388506
|
T | A | 1 | a0001c0002t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.144-3970T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388506 | ||||||
| chr17:78388506
|
T | TA | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3970_144-3969i others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388506 | ||||||
| chr17:78388507
|
T | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.144-3969T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388507 | ||||||
| chr17:78388512
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-3964T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388512 | ||||||
| chr17:78388513
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-3963A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388513 | ||||||
| chr17:78388599
|
G | A | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-3877G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388599 | ||||||
| chr17:78388662
|
G | A | 14 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(11): Show | 14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-3814G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388662 | ||||||
| chr17:78388760
|
C | T | 14 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(11): Show | 14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-3716C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388760 | ||||||
| chr17:78388816
|
A | ACTGT | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3658_144-3657i others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78388816 | |||||
| chr17:78388940
|
C | T | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-3536C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388940 | ||||||
| chr17:78388963
|
T | C | 62 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(59): Show | 62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3513T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388963 | ||||||
| chr17:78388986
|
TAAGTTGA others(2): Show |
T | 61 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3480_144-3472d others(11): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78388986 | |||||
| chr17:78389053
|
C | CT | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(119): Show | 131 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(128): Show |
intron_variant | MODIFIER | c.144-3401dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | |||||
| chr17:78389053
|
C | CTT | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0096others(28): Show | 33 | HG00140.hp1 HG00438.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.144-3402_144-3401d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | |||||
| chr17:78389053
|
C | CTTT | 16 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0280others(13): Show | 16 | HG01123.hp2 HG01952.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.144-3403_144-3401d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | |||||
| chr17:78389053
|
C | CTTTTT | 29 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0001g0344others(26): Show | 29 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.144-3405_144-3401d others(7): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | |||||
| chr17:78389053
|
C | CTTTTTT | 9 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0339others(6): Show | 9 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-3406_144-3401d others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | |||||
| chr17:78389053
|
CT | C | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(72): Show | 78 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.144-3401delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | |||||
| chr17:78389075
|
T | G | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.144-3401T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389075 | ||||||
| chr17:78389076
|
G | C | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.144-3400G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389076 | ||||||
| chr17:78389077
|
C | G | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.144-3399C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389077 | ||||||
| chr17:78389080
|
G | T | 62 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(59): Show | 62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3396G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389080 | ||||||
| chr17:78389119
|
A | AT | 21 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0088others(18): Show | 22 | HG02129.hp1 HG02165.hp2 NA18941.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-3356dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389119 | |||||
| chr17:78389127
|
A | G | 8 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(5): Show | 8 | HG01243.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.144-3349A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389127 | ||||||
| chr17:78389186
|
C | T | 60 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(57): Show | 60 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.144-3290C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389186 | ||||||
| chr17:78389229
|
T | C | 62 | a0001c0001t0001g0229a0001c0001t0001g0333a0001c0001t0001g0334others(59): Show | 62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3247T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389229 | ||||||
| chr17:78389250
|
C | A | 61 | a0001c0001t0001g0229a0001c0001t0001g0333a0001c0001t0001g0334others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3226C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389250 | ||||||
| chr17:78389300
|
C | T | 62 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(59): Show | 62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3176C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389300 | ||||||
| chr17:78389331
|
G | A | 1 | a0001c0002t0001g0115 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.144-3145G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389331 | ||||||
| chr17:78389337
|
G | A | 13 | a0001c0003t0001g0077a0001c0003t0002g0079a0001c0003t0002g0176others(10): Show | 13 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.144-3139G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389337 | ||||||
| chr17:78389411
|
T | C | 9 | a0001c0002t0001g0186a0001c0002t0001g0192a0001c0002t0002g0189others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-3065T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389411 | ||||||
| chr17:78389474
|
C | T | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.144-3002C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389474 | ||||||
| chr17:78389501
|
A | G | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-2975A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389501 | ||||||
| chr17:78389574
|
GCCTCCCA others(6): Show |
G | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-2901_144-2889d others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389574 | ||||||
| chr17:78389622
|
C | CT | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(200): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.144-2845dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389622 | |||||
| chr17:78389622
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.144-2854C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389622 | ||||||
| chr17:78389636
|
C | G | 1 | a0001c0001t0001g0278 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.144-2840C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389636 | ||||||
| chr17:78389642
|
C | A | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.144-2834C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389642 | ||||||
| chr17:78389744
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.144-2732G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389744 | ||||||
| chr17:78389804
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.144-2672C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389804 | ||||||
| chr17:78389891
|
T | C | 1 | a0001c0003t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144-2585T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389891 | ||||||
| chr17:78389956
|
A | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.144-2520A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389956 | ||||||
| chr17:78389978
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144-2498G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389978 | ||||||
| chr17:78389986
|
A | G | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-2490A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389986 | ||||||
| chr17:78390008
|
G | T | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.144-2468G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390008 | ||||||
| chr17:78390062
|
T | TCCCCCCG others(8): Show |
2 | a0001c0001t0001g0266a0001c0011t0002g0315 | 2 | HG01256.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.144-2409_144-2408i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCCG others(9): Show |
2 | a0001c0001t0001g0219a0001c0001t0001g0251 | 2 | HG00438.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.144-2409_144-2408i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(8): Show |
1 | a0001c0001t0001g0324 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.144-2403_144-2402i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(9): Show |
4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0253others(1): Show | 4 | HG01099.hp1 HG02738.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2403_144-2402i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(6): Show |
1 | a0001c0001t0001g0108 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-2402_144-2401i others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(9): Show |
1 | a0001c0001t0001g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.144-2402_144-2401i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(7): Show |
51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 58 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(8): Show |
76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0090others(73): Show | 80 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(13): Show |
1 | a0001c0001t0001g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.144-2402_144-2401i others(22): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(9): Show |
14 | a0001c0001t0001g0099a0001c0001t0001g0214a0001c0001t0001g0217others(11): Show | 14 | HG00639.hp1 HG00735.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(10): Show |
5 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0301others(2): Show | 5 | HG01070.hp1 HG02451.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(19): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390062
|
T | TCCCCCGC others(8): Show |
1 | a0001c0001t0001g0289 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.144-2404_144-2403i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | |||||
| chr17:78390067
|
C | CGCCCCCG others(8): Show |
6 | a0001c0001t0001g0344a0001c0001t0001g0360a0001c0001t0001g0361others(3): Show | 6 | HG00609.hp1 HG01109.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390067 | |||||
| chr17:78390067
|
C | CGCCCCCG others(7): Show |
41 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390067 | |||||
| chr17:78390068
|
G | A | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-2408G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390068 | ||||||
| chr17:78390148
|
C | G | 6 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(3): Show | 6 | NA18612.hp1 NA18941.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-2328C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390148 | ||||||
| chr17:78390193
|
C | A | 77 | a0001c0001t0001g0152a0001c0002t0001g0001a0001c0002t0001g0007others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.144-2283C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390193 | ||||||
| chr17:78390237
|
C | A | 1 | a0001c0001t0003g0341 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.144-2239C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390237 | ||||||
| chr17:78390254
|
C | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(203): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.144-2222C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390254 | ||||||
| chr17:78390266
|
A | G | 1 | a0003c0005t0001g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.144-2210A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390266 | ||||||
| chr17:78390324
|
GT | G | 9 | a0001c0001t0001g0362a0001c0003t0002g0177a0001c0003t0002g0178others(6): Show | 9 | HG02630.hp2 HG02818.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-2151delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390324 | ||||||
| chr17:78390325
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.144-2151T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390325 | ||||||
| chr17:78390325
|
T | G | 41 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.144-2151T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390325 | ||||||
| chr17:78390325
|
T | TG | 11 | a0001c0002t0001g0167a0001c0002t0001g0186a0001c0002t0001g0192others(8): Show | 11 | HG01099.hp2 HG01175.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-2146dupG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390325 | |||||
| chr17:78390326
|
G | T | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.144-2150G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390326 | ||||||
| chr17:78390328
|
GGGA | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.144-2144_144-2142d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390328 | |||||
| chr17:78390331
|
A | G | 189 | a0001c0001t0001g0152a0001c0001t0001g0337a0001c0001t0001g0338others(186): Show | 196 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.144-2145A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390331 | ||||||
| chr17:78390332
|
GGAA | G | 42 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(39): Show | 42 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.144-2143_144-2141d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390332 | ||||||
| chr17:78390335
|
A | G | 5 | a0001c0001t0001g0338a0001c0001t0001g0350a0001c0001t0001g0364others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-2141A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390335 | ||||||
| chr17:78390368
|
C | T | 2 | a0001c0002t0001g0160a0001c0002t0001g0161 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.144-2108C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390368 | ||||||
| chr17:78390497
|
G | T | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-1979G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390497 | ||||||
| chr17:78390516
|
C | G | 2 | a0001c0001t0001g0346a0001c0001t0001g0348 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.144-1960C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390516 | ||||||
| chr17:78390625
|
G | A | 3 | a0001c0002t0001g0113a0001c0002t0001g0136a0001c0002t0001g0144 | 3 | NA18946.hp2 NA18961.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.144-1851G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390625 | ||||||
| chr17:78390678
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.144-1798C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390678 | ||||||
| chr17:78390703
|
G | C | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | NA18982.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.144-1773G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390703 | ||||||
| chr17:78390728
|
C | T | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-1748C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390728 | ||||||
| chr17:78390802
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.144-1674C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390802 | ||||||
| chr17:78390817
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.144-1659C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390817 | ||||||
| chr17:78390834
|
C | T | 44 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(41): Show | 44 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.144-1642C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390834 | ||||||
| chr17:78390837
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.144-1639T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390837 | ||||||
| chr17:78390903
|
A | T | 73 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(70): Show | 76 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.144-1573A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390903 | ||||||
| chr17:78391022
|
T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.144-1454T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391022 | ||||||
| chr17:78391163
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.144-1313A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391163 | ||||||
| chr17:78391193
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(182): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.144-1283A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391193 | ||||||
| chr17:78391241
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.144-1235C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391241 | ||||||
| chr17:78391282
|
G | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(135): Show | 148 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.144-1194G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391282 | ||||||
| chr17:78391295
|
C | T | 44 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(41): Show | 44 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.144-1181C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391295 | ||||||
| chr17:78391563
|
C | T | 1 | a0001c0002t0001g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.144-913C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391563 | ||||||
| chr17:78391611
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.144-865G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391611 | ||||||
| chr17:78391897
|
T | C | 1 | a0001c0001t0001g0012 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.144-579T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391897 | ||||||
| chr17:78391913
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.144-563C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391913 | ||||||
| chr17:78391961
|
GGTGCTTC others(8): Show |
G | 1 | a0001c0001t0001g0303 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.144-513_144-499del others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78391961 | |||||
| chr17:78392054
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.144-422C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392054 | ||||||
| chr17:78392121
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(190): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.144-355A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392121 | ||||||
| chr17:78392164
|
G | A | 15 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(12): Show | 15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.144-312G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392164 | ||||||
| chr17:78392246
|
C | T | 1 | a0001c0002t0001g0156 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.144-230C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392246 | ||||||
| chr17:78392262
|
T | C | 5 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0235others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-214T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392262 | ||||||
| chr17:78392401
|
A | G | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.144-75A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392401 | ||||||
| chr17:78392421
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.144-55G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392421 | ||||||
| chr17:78392755
|
T | C | 11 | a0001c0003t0002g0176a0001c0003t0002g0177a0001c0003t0002g0178others(8): Show | 11 | HG02055.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.333+90T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78392755 | ||||||
| chr17:78392970
|
A | T | 2 | a0001c0002t0001g0160a0001c0002t0001g0161 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.333+305A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78392970 | ||||||
| chr17:78393039
|
C | T | 47 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+374C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393039 | ||||||
| chr17:78393047
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.333+382G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393047 | ||||||
| chr17:78393063
|
C | CT | 10 | a0001c0001t0001g0096a0001c0001t0001g0282a0001c0002t0001g0109others(7): Show | 10 | HG01109.hp1 HG01952.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+413dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393063 | |||||
| chr17:78393063
|
CT | C | 48 | a0001c0001t0001g0108a0001c0001t0001g0333a0001c0001t0001g0334others(45): Show | 48 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.333+413delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393063 | |||||
| chr17:78393083
|
T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.333+418T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393083 | ||||||
| chr17:78393095
|
C | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(181): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.333+430C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393095 | ||||||
| chr17:78393125
|
A | G | 6 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(3): Show | 6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+460A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393125 | ||||||
| chr17:78393146
|
C | T | 1 | a0001c0001t0015g0300 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.333+481C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393146 | ||||||
| chr17:78393209
|
T | C | 375 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(372): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.333+544T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393209 | ||||||
| chr17:78393247
|
A | T | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0064 | 3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+582A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393247 | ||||||
| chr17:78393248
|
G | A | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0064 | 3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+583G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393248 | ||||||
| chr17:78393249
|
ATGGGG | A | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0064 | 3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+586_333+590del others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393249 | |||||
| chr17:78393255
|
T | C | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0064 | 3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+590T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393255 | ||||||
| chr17:78393256
|
T | A | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0064 | 3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+591T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393256 | ||||||
| chr17:78393281
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.333+616C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393281 | ||||||
| chr17:78393331
|
A | G | 1 | a0001c0002t0002g0068 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.333+666A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393331 | ||||||
| chr17:78393446
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.333+781G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393446 | ||||||
| chr17:78393457
|
T | A | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.333+792T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393457 | ||||||
| chr17:78393536
|
C | T | 2 | a0001c0002t0005g0075a0001c0002t0005g0082 | 2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.333+871C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393536 | ||||||
| chr17:78393912
|
TGG | T | 379 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(376): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.333+1250_333+1251d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393912 | |||||
| chr17:78393918
|
C | T | 379 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(376): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.333+1253C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393918 | ||||||
| chr17:78393955
|
C | T | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.333+1290C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393955 | ||||||
| chr17:78393999
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.333+1334C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393999 | ||||||
| chr17:78394116
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(59): Show | 65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.333+1451A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394116 | ||||||
| chr17:78394158
|
C | T | 1 | a0001c0001t0002g0371 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.333+1493C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394158 | ||||||
| chr17:78394170
|
TC | T | 106 | a0001c0001t0001g0013a0001c0001t0001g0090a0001c0001t0001g0091others(103): Show | 107 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.333+1508delC | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78394170 | |||||
| chr17:78394170
|
TCC | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(171): Show | 187 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.333+1507_333+1508d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78394170 | |||||
| chr17:78394171
|
C | CA | 5 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0002t0001g0084others(2): Show | 5 | HG01261.hp2 HG01952.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+1506_333+1507i others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394171 | ||||||
| chr17:78394171
|
CCCA | C | 68 | a0001c0001t0001g0349a0001c0002t0001g0001a0001c0002t0001g0007others(65): Show | 72 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.333+1507_333+1509d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394171 | ||||||
| chr17:78394172
|
C | A | 30 | a0001c0001t0001g0100a0001c0001t0001g0336a0001c0001t0001g0337others(27): Show | 30 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.333+1507C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394172 | ||||||
| chr17:78394173
|
C | A | 136 | a0001c0001t0001g0013a0001c0001t0001g0090a0001c0001t0001g0091others(133): Show | 137 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.333+1508C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394173 | ||||||
| chr17:78394218
|
G | A | 1 | a0001c0002t0001g0329 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.333+1553G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394218 | ||||||
| chr17:78394651
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.334-1657G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394651 | ||||||
| chr17:78394746
|
G | T | 1 | a0001c0001t0001g0354 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.334-1562G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394746 | ||||||
| chr17:78394782
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-1526C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394782 | ||||||
| chr17:78394924
|
C | T | 73 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(70): Show | 76 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-1384C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394924 | ||||||
| chr17:78394993
|
G | A | 6 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(3): Show | 6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-1315G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394993 | ||||||
| chr17:78395051
|
AT | A | 75 | a0001c0001t0001g0152a0001c0002t0001g0001a0001c0002t0001g0007others(72): Show | 79 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.334-1256delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395051 | ||||||
| chr17:78395069
|
G | A | 14 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(11): Show | 14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-1239G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395069 | ||||||
| chr17:78395188
|
G | A | 2 | a0001c0002t0002g0200a0001c0002t0002g0201 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.334-1120G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395188 | ||||||
| chr17:78395238
|
A | G | 1 | a0001c0002t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.334-1070A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395238 | ||||||
| chr17:78395293
|
A | G | 4 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(1): Show | 4 | HG02723.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1015A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395293 | ||||||
| chr17:78395305
|
A | T | 50 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0023others(47): Show | 53 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.334-1003A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395305 | ||||||
| chr17:78395373
|
T | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(202): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.334-935T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395373 | ||||||
| chr17:78395572
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(156): Show | 170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.334-736C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395572 | ||||||
| chr17:78395583
|
A | G | 375 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(372): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.334-725A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395583 | ||||||
| chr17:78395792
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0271 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.334-516G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395792 | ||||||
| chr17:78395888
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.334-420G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395888 | ||||||
| chr17:78395894
|
A | G | 2 | a0001c0012t0008g0188a0001c0013t0011g0187 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.334-414A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395894 | ||||||
| chr17:78395952
|
C | G | 5 | a0001c0002t0001g0111a0001c0002t0001g0165a0001c0002t0001g0166others(2): Show | 5 | HG00140.hp2 HG00741.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-356C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395952 | ||||||
| chr17:78395998
|
C | T | 1 | a0001c0002t0001g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.334-310C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395998 | ||||||
| chr17:78396063
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 166 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.334-245G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78396063 | ||||||
| chr17:78396107
|
G | A | 1 | a0001c0003t0002g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.334-201G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78396107 | ||||||
| chr17:78396211
|
C | T | 1 | a0001c0002t0002g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.334-97C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78396211 | ||||||
| chr17:78396444
|
A | T | 5 | a0001c0002t0001g0111a0001c0002t0001g0165a0001c0002t0001g0166others(2): Show | 5 | HG00140.hp2 HG00741.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+59A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396444 | ||||||
| chr17:78396675
|
C | G | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(71): Show | 77 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.411+290C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396675 | ||||||
| chr17:78396885
|
T | C | 9 | a0001c0002t0001g0186a0001c0002t0001g0192a0001c0002t0002g0189others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+500T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396885 | ||||||
| chr17:78396946
|
T | C | 1 | a0001c0003t0016g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.411+561T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396946 | ||||||
| chr17:78396949
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.411+564T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396949 | ||||||
| chr17:78396996
|
CGGACCTG others(6): Show |
C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.411+612_411+624del others(13): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396996 | ||||||
| chr17:78397167
|
G | T | 3 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | HG02922.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.411+782G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397167 | ||||||
| chr17:78397289
|
A | ACAGACGG others(97): Show |
76 | a0001c0001t0001g0152a0001c0002t0001g0001a0001c0002t0001g0007others(73): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.411+905_412-859dup others(104): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397289 | |||||
| chr17:78397291
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.411+906A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397291 | ||||||
| chr17:78397291
|
A | GGACGGGC others(97): Show |
1 | a0001c0002t0004g0173 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.411+905_411+906ins others(104): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397291 | ||||||
| chr17:78397307
|
CAG | C | 3 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | HG02922.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.411+925_411+926del others(2): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397307 | |||||
| chr17:78397332
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.412-920G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397332 | ||||||
| chr17:78397441
|
C | CT | 13 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0133others(10): Show | 14 | HG00408.hp2 HG00558.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.412-799dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397441 | |||||
| chr17:78397458
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.412-794C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397458 | ||||||
| chr17:78397589
|
A | AC | 49 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.412-656dupC | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397589 | |||||
| chr17:78397589
|
A | ACCC | 55 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(52): Show | 58 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.412-658_412-656dup others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397589 | |||||
| chr17:78397589
|
A | ACCCC | 21 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG00438.hp1 HG01106.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.412-659_412-656dup others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397589 | |||||
| chr17:78397594
|
C | CCCG | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(79): Show | 90 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.412-656_412-655ins others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397594 | |||||
| chr17:78397655
|
AAAC | A | 49 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0023others(46): Show | 52 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.412-596_412-594del others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397655 | ||||||
| chr17:78397663
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412-589G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397663 | ||||||
| chr17:78397681
|
C | T | 8 | a0001c0001t0001g0335a0001c0001t0001g0354a0001c0001t0001g0358others(5): Show | 8 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-571C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397681 | ||||||
| chr17:78397704
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.412-548G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397704 | ||||||
| chr17:78397815
|
C | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.412-437C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397815 | ||||||
| chr17:78397894
|
G | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.412-358G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397894 | ||||||
| chr17:78397932
|
G | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.412-320G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397932 | ||||||
| chr17:78397960
|
C | T | 1 | a0001c0012t0008g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.412-292C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397960 | ||||||
| chr17:78397961
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.412-291G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397961 | ||||||
| chr17:78397994
|
A | G | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.412-258A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397994 | ||||||
| chr17:78398078
|
A | G | 16 | a0001c0001t0001g0340a0001c0003t0001g0077a0001c0003t0002g0024others(13): Show | 16 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.412-174A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398078 | ||||||
| chr17:78398096
|
A | G | 3 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326 | 3 | HG02148.hp1 NA18966.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.412-156A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398096 | ||||||
| chr17:78398114
|
T | C | 76 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(73): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.412-138T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398114 | ||||||
| chr17:78398124
|
G | T | 6 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0349others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-128G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398124 | ||||||
| chr17:78398199
|
A | G | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.412-53A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398199 | ||||||
| chr17:78398232
|
T | C | 1 | a0001c0003t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.412-20T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398232 | ||||||
| chr17:78398368
|
C | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.511+17C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398368 | ||||||
| chr17:78398445
|
T | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.511+94T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398445 | ||||||
| chr17:78398514
|
T | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.511+163T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398514 | ||||||
| chr17:78398583
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.511+232G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398583 | ||||||
| chr17:78398640
|
C | T | 1 | a0001c0002t0001g0050 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511+289C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398640 | ||||||
| chr17:78398888
|
G | C | 4 | a0001c0002t0001g0083a0001c0002t0001g0118a0001c0002t0001g0119others(1): Show | 4 | HG02132.hp1 NA18983.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-460G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398888 | ||||||
| chr17:78398957
|
A | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.512-391A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398957 | ||||||
| chr17:78399088
|
T | C | 73 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(70): Show | 76 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.512-260T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399088 | ||||||
| chr17:78399116
|
G | A | 6 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(3): Show | 6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-232G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399116 | ||||||
| chr17:78399284
|
C | T | 1 | a0001c0001t0004g0357 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.512-64C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399284 | ||||||
| chr17:78399289
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.512-59T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399289 | ||||||
| chr17:78399327
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.512-21G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399327 | ||||||
| chr17:78399340
|
G | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
splice_region_variant&intron_variant | LOW | c.512-8G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399340 | ||||||
| chr17:78399553
|
C | T | 73 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(70): Show | 76 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.701+16C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399553 | ||||||
| chr17:78399568
|
C | T | 1 | a0001c0002t0001g0023 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.701+31C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399568 | ||||||
| chr17:78399669
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399669 | ||||||
| chr17:78399672
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+135G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399672 | ||||||
| chr17:78399763
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701+226G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399763 | ||||||
| chr17:78399772
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0099others(1): Show | 4 | NA18960.hp2 NA18963.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+235G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399772 | ||||||
| chr17:78399775
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+238A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399775 | ||||||
| chr17:78399795
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.701+258C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399795 | ||||||
| chr17:78399899
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.701+362C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399899 | ||||||
| chr17:78399953
|
C | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0266 | 2 | NA18963.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.701+416C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399953 | ||||||
| chr17:78400083
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+546G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400083 | ||||||
| chr17:78400095
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.701+558C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400095 | ||||||
| chr17:78400107
|
C | T | 82 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(79): Show | 85 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.701+570C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400107 | ||||||
| chr17:78400239
|
G | T | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.702-438G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400239 | ||||||
| chr17:78400244
|
G | T | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-433G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400244 | ||||||
| chr17:78400245
|
T | G | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-432T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400245 | ||||||
| chr17:78400246
|
G | T | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-431G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400246 | ||||||
| chr17:78400277
|
C | T | 1 | a0001c0003t0002g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.702-400C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400277 | ||||||
| chr17:78400293
|
G | T | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-384G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400293 | ||||||
| chr17:78400382
|
C | CA | 69 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348others(66): Show | 72 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.702-282dupA | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 78400382 | |||||
| chr17:78400382
|
C | CAA | 7 | a0001c0002t0001g0031a0001c0002t0001g0051a0001c0002t0001g0058others(4): Show | 7 | HG00408.hp1 HG02523.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-283_702-282dup others(2): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 78400382 | |||||
| chr17:78400447
|
C | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.702-230C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400447 | ||||||
| chr17:78400529
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.702-148G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400529 | ||||||
| chr17:78400543
|
G | C | 1 | a0001c0002t0001g0032 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.702-134G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400543 | ||||||
| chr17:78400881
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0299 | 2 | NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.880+26T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78400881 | ||||||
| chr17:78400882
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+27A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78400882 | ||||||
| chr17:78401047
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+192A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401047 | ||||||
| chr17:78401052
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+197A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401052 | ||||||
| chr17:78401095
|
G | A | 81 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(78): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.880+240G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401095 | ||||||
| chr17:78401138
|
A | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+283A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401138 | ||||||
| chr17:78401211
|
A | T | 3 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326 | 3 | HG02148.hp1 NA18966.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.880+356A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401211 | ||||||
| chr17:78401228
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+373C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401228 | ||||||
| chr17:78401253
|
A | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+398A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401253 | ||||||
| chr17:78401262
|
G | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.880+407G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401262 | ||||||
| chr17:78401333
|
T | G | 4 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(1): Show | 4 | HG02723.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.880+478T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401333 | ||||||
| chr17:78401389
|
C | T | 3 | a0001c0002t0001g0058a0001c0002t0001g0061a0001c0002t0001g0066 | 3 | NA18959.hp1 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.880+534C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401389 | ||||||
| chr17:78401702
|
G | T | 1 | a0002c0004t0001g0194 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.880+847G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401702 | ||||||
| chr17:78401731
|
G | A | 1 | a0001c0002t0001g0029 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.880+876G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401731 | ||||||
| chr17:78401749
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+894T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401749 | ||||||
| chr17:78401787
|
G | C | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.880+932G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401787 | ||||||
| chr17:78401814
|
A | T | 2 | a0001c0002t0002g0200a0001c0002t0002g0201 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.880+959A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401814 | ||||||
| chr17:78401869
|
TG | T | 22 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(19): Show | 22 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.880+1015delG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401869 | ||||||
| chr17:78401912
|
C | T | 4 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(1): Show | 4 | HG02723.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.880+1057C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401912 | ||||||
| chr17:78401977
|
C | A | 1 | a0001c0001t0002g0263 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.880+1122C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401977 | ||||||
| chr17:78401977
|
C | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.880+1122C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401977 | ||||||
| chr17:78402020
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1165A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402020 | ||||||
| chr17:78402043
|
GTGT | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1189_880+1191d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402043 | ||||||
| chr17:78402049
|
G | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1194G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402049 | ||||||
| chr17:78402051
|
AG | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1199delG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402051 | |||||
| chr17:78402076
|
G | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1221G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402076 | ||||||
| chr17:78402187
|
G | T | 1 | a0001c0001t0001g0359 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.880+1332G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402187 | ||||||
| chr17:78402223
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(142): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.881-1345G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402223 | ||||||
| chr17:78402323
|
G | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.881-1245G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402323 | ||||||
| chr17:78402373
|
A | T | 1 | a0001c0001t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.881-1195A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402373 | ||||||
| chr17:78402397
|
CATATATA others(1): Show |
C | 3 | a0001c0002t0001g0064a0001c0002t0002g0065a0001c0002t0002g0076 | 3 | HG04228.hp2 NA19074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.881-1147_881-1140d others(10): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402397 | |||||
| chr17:78402397
|
CATATATA others(3): Show |
C | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0017others(68): Show | 74 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.881-1149_881-1140d others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402397 | |||||
| chr17:78402397
|
CATATATA others(5): Show |
C | 3 | a0001c0002t0001g0114a0001c0002t0001g0143a0001c0002t0001g0153 | 3 | HG00673.hp1 NA19004.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.881-1151_881-1140d others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402397 | |||||
| chr17:78402411
|
TATATATA others(11): Show |
T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.881-1155_881-1138d others(20): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402411 | |||||
| chr17:78402411
|
TATATATA others(13): Show |
T | 49 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.881-1155_881-1136d others(22): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402411 | |||||
| chr17:78402413
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.881-1153_881-1138d others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402413 | |||||
| chr17:78402413
|
TATATATA others(11): Show |
T | 14 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(11): Show | 14 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.881-1153_881-1136d others(20): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402413 | |||||
| chr17:78402415
|
TATATATA others(7): Show |
T | 1 | a0001c0002t0001g0118 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.881-1151_881-1138d others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402415 | |||||
| chr17:78402417
|
TATATATA others(5): Show |
T | 81 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(78): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.881-1149_881-1138d others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402417 | |||||
| chr17:78402419
|
TATATATA others(3): Show |
T | 8 | a0001c0002t0001g0140a0001c0002t0001g0157a0001c0002t0001g0158others(5): Show | 8 | HG01175.hp1 HG02723.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.881-1147_881-1138d others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402419 | |||||
| chr17:78402427
|
T | C | 5 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0042others(2): Show | 5 | HG00738.hp1 HG04228.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-1141T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402427 | ||||||
| chr17:78402429
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.881-1139C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402429 | ||||||
| chr17:78402436
|
A | G | 1 | a0001c0002t0002g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.881-1132A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402436 | ||||||
| chr17:78402506
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.881-1062G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402506 | ||||||
| chr17:78402555
|
C | T | 3 | a0001c0002t0001g0111a0001c0002t0001g0166a0001c0002t0001g0171 | 3 | HG00140.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.881-1013C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402555 | ||||||
| chr17:78402748
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881-820C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402748 | ||||||
| chr17:78402813
|
T | C | 23 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(20): Show | 23 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.881-755T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402813 | ||||||
| chr17:78402996
|
C | T | 3 | a0001c0001t0002g0014a0001c0001t0002g0270a0001c0001t0002g0304 | 4 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-572C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402996 | ||||||
| chr17:78403015
|
C | G | 1 | a0001c0002t0002g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.881-553C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403015 | ||||||
| chr17:78403077
|
G | T | 1 | a0001c0012t0008g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.881-491G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403077 | ||||||
| chr17:78403323
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.881-245C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403323 | ||||||
| chr17:78403364
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.881-204T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403364 | ||||||
| chr17:78403470
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.881-98C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403470 | ||||||
| chr17:78403471
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.881-97G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403471 | ||||||
| chr17:78403557
|
G | A | 8 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(5): Show | 8 | HG02145.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.881-11G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403557 | ||||||
| chr17:78404093
|
C | A | 1 | a0001c0001t0001g0359 | 1 | HG01433.hp2 | splice_region_variant&intron_variant | LOW | c.1402+4C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404093 | ||||||
| chr17:78404140
|
T | C | 40 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(37): Show | 40 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1402+51T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404140 | ||||||
| chr17:78404149
|
G | A | 62 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(59): Show | 65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1402+60G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404149 | ||||||
| chr17:78404155
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(196): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+66G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404155 | ||||||
| chr17:78404170
|
C | G | 76 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(73): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1402+81C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404170 | ||||||
| chr17:78404177
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(196): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+88G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404177 | ||||||
| chr17:78404187
|
C | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(196): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+98C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404187 | ||||||
| chr17:78404240
|
A | G | 80 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(77): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1402+151A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404240 | ||||||
| chr17:78404246
|
TGGG | T | 5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+159_1402+161d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404246 | |||||
| chr17:78404248
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(191): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1402+159G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404248 | ||||||
| chr17:78404256
|
C | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1402+167C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404256 | ||||||
| chr17:78404279
|
A | AT | 12 | a0001c0002t0001g0128a0001c0002t0001g0130a0001c0002t0001g0131others(9): Show | 12 | HG00544.hp1 HG01175.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1402+212dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | |||||
| chr17:78404279
|
AT | A | 88 | a0001c0001t0001g0339a0001c0001t0001g0344a0001c0001t0001g0361others(85): Show | 91 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1402+212delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | |||||
| chr17:78404279
|
ATTT | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0243a0001c0001t0001g0374others(3): Show | 6 | HG02055.hp1 HG02615.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+210_1402+212d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | |||||
| chr17:78404279
|
ATTTT | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1402+209_1402+212d others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | |||||
| chr17:78404352
|
G | A | 1 | a0001c0003t0001g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1402+263G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404352 | ||||||
| chr17:78404368
|
A | C | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1402+279A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404368 | ||||||
| chr17:78404426
|
G | A | 73 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(70): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1402+337G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404426 | ||||||
| chr17:78404485
|
G | T | 81 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0008others(78): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1402+396G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404485 | ||||||
| chr17:78404628
|
G | C | 15 | a0001c0003t0001g0077a0001c0003t0002g0024a0001c0003t0002g0079others(12): Show | 15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402+539G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404628 | ||||||
| chr17:78404641
|
C | T | 2 | a0001c0002t0001g0041a0001c0002t0001g0218 | 2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1402+552C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404641 | ||||||
| chr17:78404709
|
G | A | 1 | a0001c0001t0001g0377 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1402+620G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404709 | ||||||
| chr17:78404952
|
G | A | 6 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0159others(3): Show | 6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+863G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404952 | ||||||
| chr17:78405152
|
TA | T | 18 | a0001c0001t0001g0335a0001c0001t0001g0353a0001c0001t0001g0354others(15): Show | 18 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1402+1064delA | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405152 | ||||||
| chr17:78405205
|
C | T | 1 | a0001c0001t0002g0345 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1402+1116C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405205 | ||||||
| chr17:78405237
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(196): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+1148C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405237 | ||||||
| chr17:78405247
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(156): Show | 170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1402+1158C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405247 | ||||||
| chr17:78405248
|
A | G | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1402+1159A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405248 | ||||||
| chr17:78405275
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1402+1186C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405275 | ||||||
| chr17:78405349
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0006g0224 | 2 | HG00733.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1402+1260C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405349 | ||||||
| chr17:78405406
|
T | G | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1402+1317T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405406 | ||||||
| chr17:78405635
|
C | G | 1 | a0001c0002t0007g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1402+1546C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405635 | ||||||
| chr17:78405689
|
C | T | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1402+1600C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405689 | ||||||
| chr17:78405773
|
A | C | 2 | a0001c0003t0002g0176a0001c0003t0008g0016 | 2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1402+1684A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405773 | ||||||
| chr17:78405820
|
C | A | 1 | a0001c0001t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1402+1731C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405820 | ||||||
| chr17:78406024
|
A | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1402+1935A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406024 | ||||||
| chr17:78406035
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(80): Show | 91 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.1402+1946G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406035 | ||||||
| chr17:78406041
|
GCGCGGTG others(5): Show |
G | 13 | a0001c0002t0001g0001a0001c0002t0001g0111a0001c0002t0001g0155others(10): Show | 15 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.1402+1956_1402+196 others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78406041 | |||||
| chr17:78406186
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1402+2097C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406186 | ||||||
| chr17:78406187
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1402+2098G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406187 | ||||||
| chr17:78406190
|
C | G | 1 | a0001c0002t0001g0127 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1402+2101C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406190 | ||||||
| chr17:78406284
|
T | C | 375 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(372): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1402+2195T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406284 | ||||||
| chr17:78406309
|
C | T | 3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | HG02145.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1402+2220C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406309 | ||||||
| chr17:78406498
|
G | A | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402+2409G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406498 | ||||||
| chr17:78406546
|
G | C | 1 | a0001c0002t0001g0148 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1402+2457G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406546 | ||||||
| chr17:78406591
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1402+2502A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406591 | ||||||
| chr17:78406671
|
T | C | 2 | a0001c0001t0003g0341a0001c0001t0005g0342 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1402+2582T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406671 | ||||||
| chr17:78406947
|
T | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(202): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1402+2858T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406947 | ||||||
| chr17:78406984
|
C | A | 1 | a0001c0001t0001g0356 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1402+2895C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406984 | ||||||
| chr17:78407038
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0242 | 2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1402+2949A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407038 | ||||||
| chr17:78407473
|
C | G | 3 | a0001c0001t0002g0330a0001c0001t0003g0331a0001c0001t0003g0332 | 3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402+3384C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407473 | ||||||
| chr17:78407509
|
C | A | 25 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(22): Show | 25 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1402+3420C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407509 | ||||||
| chr17:78407617
|
G | A | 7 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0002g0199others(4): Show | 7 | HG01069.hp2 HG01243.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1402+3528G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407617 | ||||||
| chr17:78407677
|
A | G | 1 | a0001c0003t0002g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1402+3588A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407677 | ||||||
| chr17:78407779
|
G | A | 2 | a0001c0002t0001g0165a0001c0007t0006g0170 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1402+3690G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407779 | ||||||
| chr17:78407822
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1402+3733G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407822 | ||||||
| chr17:78407842
|
G | C | 1 | a0001c0002t0001g0042 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1402+3753G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407842 | ||||||
| chr17:78407903
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(156): Show | 170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1402+3814G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407903 | ||||||
| chr17:78408044
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1402+3955G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408044 | ||||||
| chr17:78408077
|
A | G | 1 | a0001c0003t0002g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1402+3988A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408077 | ||||||
| chr17:78408108
|
ATCAG | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(156): Show | 170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1402+4023_1402+402 others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78408108 | |||||
| chr17:78408199
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(59): Show | 65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1402+4110A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408199 | ||||||
| chr17:78408351
|
G | A | 11 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0029others(8): Show | 11 | HG00544.hp2 HG02015.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+4262G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408351 | ||||||
| chr17:78408445
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1402+4356G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408445 | ||||||
| chr17:78408499
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1402+4410C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408499 | ||||||
| chr17:78408574
|
C | T | 42 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(39): Show | 42 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1402+4485C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408574 | ||||||
| chr17:78408660
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1402+4571G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408660 | ||||||
| chr17:78408705
|
C | T | 44 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(41): Show | 44 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1402+4616C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408705 | ||||||
| chr17:78408812
|
C | T | 73 | a0001c0001t0001g0348a0001c0002t0001g0001a0001c0002t0001g0007others(70): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1402+4723C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408812 | ||||||
| chr17:78408817
|
C | T | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1402+4728C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408817 | ||||||
| chr17:78408952
|
G | C | 5 | a0001c0002t0001g0113a0001c0002t0001g0122a0001c0002t0001g0136others(2): Show | 5 | NA18946.hp2 NA18950.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+4863G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408952 | ||||||
| chr17:78408993
|
G | A | 1 | a0001c0002t0001g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1402+4904G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408993 | ||||||
| chr17:78409077
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1402+4988G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409077 | ||||||
| chr17:78409095
|
T | C | 2 | a0001c0002t0001g0041a0001c0002t0001g0218 | 2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1402+5006T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409095 | ||||||
| chr17:78409134
|
A | G | 1 | a0001c0002t0001g0021 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1402+5045A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409134 | ||||||
| chr17:78409221
|
C | T | 44 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(41): Show | 44 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1402+5132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409221 | ||||||
| chr17:78409228
|
C | T | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1402+5139C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409228 | ||||||
| chr17:78409491
|
C | A | 1 | a0001c0001t0001g0359 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1403-5388C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409491 | ||||||
| chr17:78409565
|
G | A | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1403-5314G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409565 | ||||||
| chr17:78409655
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1403-5224T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409655 | ||||||
| chr17:78409756
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1403-5123T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409756 | ||||||
| chr17:78409830
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1403-5049G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409830 | ||||||
| chr17:78409880
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1403-4999G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409880 | ||||||
| chr17:78409947
|
C | G | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1403-4932C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409947 | ||||||
| chr17:78410003
|
C | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 203 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1403-4876C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410003 | ||||||
| chr17:78410089
|
T | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1403-4790T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410089 | ||||||
| chr17:78410103
|
AAAAAC | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(156): Show | 170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1403-4754_1403-475 others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410103 | |||||
| chr17:78410193
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0249a0001c0001t0001g0287 | 3 | HG02080.hp1 NA18948.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1403-4686A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410193 | ||||||
| chr17:78410220
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1403-4659G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410220 | ||||||
| chr17:78410290
|
A | G | 6 | a0001c0001t0001g0355a0001c0002t0001g0207a0001c0003t0002g0179others(3): Show | 6 | HG02818.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1403-4589A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410290 | ||||||
| chr17:78410316
|
C | T | 3 | a0001c0002t0001g0109a0001c0002t0007g0015a0001c0002t0007g0110 | 3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1403-4563C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410316 | ||||||
| chr17:78410321
|
C | CAGG | 73 | a0001c0001t0001g0292a0001c0001t0001g0296a0001c0001t0002g0330others(70): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1403-4554_1403-455 others(7): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410321 | |||||
| chr17:78410326
|
G | A | 10 | a0001c0002t0001g0186a0001c0002t0001g0192a0001c0002t0002g0189others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403-4553G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410326 | ||||||
| chr17:78410462
|
CT | C | 23 | a0001c0001t0002g0014a0001c0002t0001g0001a0001c0002t0001g0005others(20): Show | 27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-4388delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTT | C | 9 | a0001c0001t0001g0344a0001c0002t0001g0023a0001c0002t0001g0030others(6): Show | 9 | HG00639.hp2 HG02970.hp2 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403-4392_1403-438 others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTT | C | 57 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0100others(54): Show | 60 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-4393_1403-438 others(10): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTTT | C | 131 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(128): Show | 134 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1403-4394_1403-438 others(11): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0108a0001c0001t0001g0265a0001c0001t0001g0353others(4): Show | 7 | HG01109.hp1 HG01978.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-4395_1403-438 others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTTT others(2): Show |
C | 23 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(20): Show | 23 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1403-4396_1403-438 others(13): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTTT others(3): Show |
C | 14 | a0001c0001t0001g0276a0001c0001t0001g0346a0001c0001t0001g0347others(11): Show | 14 | HG01243.hp1 HG02258.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1403-4397_1403-438 others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTTT others(4): Show |
C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(94): Show | 105 | HG00323.hp1 HG00438.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1403-4398_1403-438 others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410462
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1403-4404_1403-438 others(21): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | |||||
| chr17:78410525
|
A | G | 379 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(376): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1403-4354A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410525 | ||||||
| chr17:78410535
|
G | A | 379 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(376): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1403-4344G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410535 | ||||||
| chr17:78410561
|
C | G | 6 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0270others(3): Show | 7 | HG01516.hp2 HG01517.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-4318C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410561 | ||||||
| chr17:78410611
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1403-4268T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410611 | ||||||
| chr17:78410624
|
C | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0347a0001c0001t0003g0331others(3): Show | 6 | HG02055.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403-4255C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410624 | ||||||
| chr17:78410630
|
T | C | 2 | a0001c0001t0001g0340a0001c0001t0001g0351 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1403-4249T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410630 | ||||||
| chr17:78410691
|
T | C | 36 | a0001c0001t0001g0274a0001c0001t0001g0280a0001c0001t0001g0289others(33): Show | 38 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1403-4188T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410691 | ||||||
| chr17:78410721
|
C | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(39): Show | 50 | HG00408.hp2 HG00558.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1403-4158C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410721 | ||||||
| chr17:78410752
|
T | G | 13 | a0001c0001t0001g0281a0001c0001t0001g0347a0001c0001t0001g0376others(10): Show | 13 | HG01123.hp2 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1403-4127T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410752 | ||||||
| chr17:78410876
|
T | C | 47 | a0001c0001t0001g0231a0001c0001t0001g0281a0001c0001t0001g0297others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1403-4003T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410876 | ||||||
| chr17:78410915
|
G | A | 1 | a0001c0002t0001g0125 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1403-3964G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410915 | ||||||
| chr17:78410986
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1403-3893G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410986 | ||||||
| chr17:78411013
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1403-3866G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411013 | ||||||
| chr17:78411082
|
G | T | 376 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(373): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1403-3797G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411082 | ||||||
| chr17:78411088
|
G | A | 2 | a0001c0002t0001g0109a0001c0002t0007g0015 | 2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1403-3791G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411088 | ||||||
| chr17:78411187
|
C | T | 1 | a0001c0002t0002g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1403-3692C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411187 | ||||||
| chr17:78411191
|
G | A | 1 | a0001c0002t0002g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1403-3688G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411191 | ||||||
| chr17:78411222
|
A | G | 376 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(373): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1403-3657A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411222 | ||||||
| chr17:78411237
|
C | T | 1 | a0001c0002t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1403-3642C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411237 | ||||||
| chr17:78411347
|
A | G | 1 | a0001c0003t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1403-3532A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411347 | ||||||
| chr17:78411417
|
G | T | 1 | a0001c0002t0001g0150 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1403-3462G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411417 | ||||||
| chr17:78411449
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0099others(2): Show | 5 | NA18959.hp2 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-3430G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411449 | ||||||
| chr17:78411545
|
C | T | 57 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(54): Show | 59 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1403-3334C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411545 | ||||||
| chr17:78411618
|
C | A | 5 | a0001c0001t0002g0345a0001c0002t0002g0073a0001c0003t0002g0024others(2): Show | 5 | HG01106.hp1 HG01123.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-3261C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411618 | ||||||
| chr17:78411707
|
T | TG | 3 | a0001c0001t0005g0342a0001c0002t0005g0075a0001c0002t0005g0082 | 3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1403-3171dupG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411707 | |||||
| chr17:78411902
|
C | CT | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(151): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1403-2949dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | |||||
| chr17:78411902
|
C | CTT | 129 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0089others(126): Show | 131 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1403-2950_1403-294 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | |||||
| chr17:78411902
|
C | CTTT | 26 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0001t0001g0091others(23): Show | 27 | HG00673.hp1 HG02486.hp2 HG02523.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-2951_1403-294 others(7): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | |||||
| chr17:78411902
|
CT | C | 25 | a0001c0001t0001g0281a0001c0001t0001g0336a0001c0001t0001g0337others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1403-2949delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | |||||
| chr17:78411902
|
CTT | C | 19 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0304others(16): Show | 20 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1403-2950_1403-294 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | |||||
| chr17:78411902
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0347 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1403-2961_1403-294 others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | |||||
| chr17:78412140
|
C | T | 3 | a0001c0001t0003g0331a0001c0001t0003g0332a0001c0001t0003g0341 | 3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1403-2739C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412140 | ||||||
| chr17:78412224
|
G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-2655G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412224 | ||||||
| chr17:78412257
|
G | A | 1 | a0001c0001t0001g0376 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1403-2622G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412257 | ||||||
| chr17:78412288
|
G | A | 31 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(28): Show | 32 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1403-2591G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412288 | ||||||
| chr17:78412305
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1403-2574G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412305 | ||||||
| chr17:78412451
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1403-2428A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412451 | ||||||
| chr17:78412536
|
G | C | 3 | a0001c0001t0005g0342a0001c0002t0005g0075a0001c0002t0005g0082 | 3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1403-2343G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412536 | ||||||
| chr17:78412621
|
C | T | 1 | a0001c0003t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1403-2258C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412621 | ||||||
| chr17:78412726
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0099others(2): Show | 5 | NA18959.hp2 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-2153G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412726 | ||||||
| chr17:78412903
|
G | A | 5 | a0001c0001t0001g0237a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG01109.hp2 HG01361.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-1976G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412903 | ||||||
| chr17:78412945
|
A | G | 15 | a0001c0001t0002g0345a0001c0002t0002g0073a0001c0003t0002g0024others(12): Show | 15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1403-1934A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412945 | ||||||
| chr17:78413012
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1403-1867G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413012 | ||||||
| chr17:78413109
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1403-1770G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413109 | ||||||
| chr17:78413199
|
C | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0217a0001c0001t0001g0228others(7): Show | 11 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1403-1680C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413199 | ||||||
| chr17:78413231
|
A | G | 4 | a0001c0002t0002g0199a0001c0002t0002g0202a0001c0002t0002g0204others(1): Show | 4 | HG01069.hp2 HG01243.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403-1648A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413231 | ||||||
| chr17:78413522
|
C | T | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-1357C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413522 | ||||||
| chr17:78413529
|
T | G | 10 | a0001c0001t0009g0368a0001c0001t0010g0352a0001c0002t0001g0058others(7): Show | 10 | HG00408.hp1 HG02523.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403-1350T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413529 | ||||||
| chr17:78413601
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1403-1278C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413601 | ||||||
| chr17:78413703
|
C | A | 3 | a0001c0001t0005g0342a0001c0002t0005g0075a0001c0002t0005g0082 | 3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1403-1176C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413703 | ||||||
| chr17:78413728
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(26): Show | 36 | HG00408.hp2 HG00558.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1403-1151G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413728 | ||||||
| chr17:78413804
|
C | T | 1 | a0001c0001t0001g0376 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1403-1075C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413804 | ||||||
| chr17:78413838
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1403-1041T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413838 | ||||||
| chr17:78414053
|
G | A | 1 | a0001c0003t0016g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1403-826G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414053 | ||||||
| chr17:78414213
|
C | G | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-666C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414213 | ||||||
| chr17:78414217
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1403-662C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414217 | ||||||
| chr17:78414261
|
C | G | 2 | a0001c0002t0001g0083a0001c0002t0001g0119 | 2 | NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1403-618C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414261 | ||||||
| chr17:78414361
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0307 | 2 | NA19083.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1403-518G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414361 | ||||||
| chr17:78414383
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1403-496G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414383 | ||||||
| chr17:78414432
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1403-447C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414432 | ||||||
| chr17:78414559
|
G | T | 1 | a0001c0001t0001g0355 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1403-320G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414559 | ||||||
| chr17:78414671
|
G | T | 4 | a0001c0002t0001g0140a0001c0002t0001g0186a0001c0003t0008g0016others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-208G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414671 | ||||||
| chr17:78414710
|
G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-169G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414710 | ||||||
| chr17:78414790
|
G | A | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(315): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1403-89G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414790 | ||||||
| chr17:78414861
|
G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-18G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414861 | ||||||
| chr17:78415073
|
T | TG | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(286): Show | 306 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.1551+51dupG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78415073 | |||||
| chr17:78415088
|
A | G | 2 | a0001c0002t0001g0140a0001c0002t0001g0186 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1551+61A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415088 | ||||||
| chr17:78415229
|
C | T | 2 | a0001c0002t0001g0140a0001c0002t0001g0186 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1551+202C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415229 | ||||||
| chr17:78415232
|
G | T | 376 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(373): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1551+205G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415232 | ||||||
| chr17:78415250
|
G | T | 1 | a0001c0001t0002g0345 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1551+223G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415250 | ||||||
| chr17:78415344
|
A | G | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1551+317A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415344 | ||||||
| chr17:78415668
|
C | T | 3 | a0001c0001t0003g0331a0001c0001t0003g0332a0001c0001t0003g0341 | 3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1551+641C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415668 | ||||||
| chr17:78415936
|
G | T | 2 | a0001c0003t0002g0176a0001c0003t0002g0180 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1551+909G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415936 | ||||||
| chr17:78415949
|
G | A | 30 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1551+922G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415949 | ||||||
| chr17:78416061
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1551+1034T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416061 | ||||||
| chr17:78416139
|
C | T | 1 | a0001c0002t0002g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1551+1112C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416139 | ||||||
| chr17:78416165
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1551+1138G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416165 | ||||||
| chr17:78416190
|
G | A | 2 | a0001c0001t0001g0339a0001c0001t0001g0353 | 2 | HG00673.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1551+1163G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416190 | ||||||
| chr17:78416267
|
T | G | 9 | a0001c0001t0001g0281a0001c0002t0001g0070a0001c0002t0001g0084others(6): Show | 9 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1551+1240T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416267 | ||||||
| chr17:78416345
|
C | G | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+1318C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416345 | ||||||
| chr17:78416416
|
G | A | 2 | a0001c0003t0008g0016a0001c0012t0008g0188 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1551+1389G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416416 | ||||||
| chr17:78416536
|
CCACTGCC others(10): Show |
C | 4 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0349others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1551+1515_1551+153 others(21): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78416536 | |||||
| chr17:78416545
|
T | C | 24 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(21): Show | 25 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1551+1518T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416545 | ||||||
| chr17:78416593
|
C | T | 1 | a0001c0002t0002g0078 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1551+1566C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416593 | ||||||
| chr17:78416594
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0002t0001g0208 | 3 | HG03831.hp1 NA18995.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1551+1567G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416594 | ||||||
| chr17:78416755
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1551+1728G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416755 | ||||||
| chr17:78416761
|
C | A | 6 | a0001c0002t0001g0084a0002c0004t0001g0190a0002c0004t0001g0191others(3): Show | 6 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1551+1734C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416761 | ||||||
| chr17:78416867
|
G | T | 7 | a0001c0001t0009g0368a0001c0001t0010g0352a0001c0002t0001g0058others(4): Show | 7 | HG00408.hp1 HG02523.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1551+1840G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416867 | ||||||
| chr17:78417106
|
C | T | 30 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1551+2079C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417106 | ||||||
| chr17:78417142
|
C | T | 15 | a0001c0001t0001g0088a0001c0001t0001g0256a0001c0001t0001g0273others(12): Show | 15 | HG01993.hp2 HG02738.hp1 NA18951.hp2 others(12): Show |
intron_variant | MODIFIER | c.1551+2115C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417142 | ||||||
| chr17:78417187
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1551+2160G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417187 | ||||||
| chr17:78417236
|
A | G | 12 | a0001c0001t0001g0231a0001c0001t0001g0335a0001c0001t0001g0354others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1551+2209A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417236 | ||||||
| chr17:78417292
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1552-2254C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417292 | ||||||
| chr17:78417395
|
C | T | 25 | a0001c0001t0001g0347a0001c0001t0002g0014a0001c0001t0002g0263others(22): Show | 26 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1552-2151C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417395 | ||||||
| chr17:78417406
|
G | A | 4 | a0001c0002t0001g0122a0001c0002t0002g0112a0001c0002t0002g0189others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-2140G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417406 | ||||||
| chr17:78417576
|
C | G | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-1970C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417576 | ||||||
| chr17:78417753
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1793G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417753 | ||||||
| chr17:78417754
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1792G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417754 | ||||||
| chr17:78417755
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1791T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417755 | ||||||
| chr17:78417756
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1790G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417756 | ||||||
| chr17:78417757
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1789G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417757 | ||||||
| chr17:78417761
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1785G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417761 | ||||||
| chr17:78417765
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1781T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417765 | ||||||
| chr17:78417766
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1780G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417766 | ||||||
| chr17:78417768
|
A | T | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1778A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417768 | ||||||
| chr17:78417769
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1777G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417769 | ||||||
| chr17:78417848
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1552-1698A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417848 | ||||||
| chr17:78417889
|
C | CAAAG | 3 | a0001c0002t0001g0058a0001c0002t0001g0061a0001c0002t0001g0066 | 3 | NA18959.hp1 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1552-1655_1552-165 others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78417889 | |||||
| chr17:78417928
|
AT | A | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(286): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1552-1597delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78417928 | |||||
| chr17:78417928
|
ATT | A | 56 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0213others(53): Show | 58 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1552-1598_1552-159 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78417928 | |||||
| chr17:78417991
|
A | G | 29 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(26): Show | 30 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1552-1555A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417991 | ||||||
| chr17:78417999
|
G | T | 1 | a0001c0002t0002g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1552-1547G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417999 | ||||||
| chr17:78418087
|
G | A | 15 | a0001c0001t0002g0345a0001c0002t0002g0073a0001c0003t0002g0024others(12): Show | 15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1552-1459G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418087 | ||||||
| chr17:78418090
|
C | T | 5 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1552-1456C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418090 | ||||||
| chr17:78418131
|
C | T | 2 | a0001c0002t0001g0140a0001c0002t0001g0186 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1552-1415C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418131 | ||||||
| chr17:78418149
|
C | T | 3 | a0001c0001t0003g0331a0001c0001t0003g0332a0001c0001t0003g0341 | 3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1552-1397C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418149 | ||||||
| chr17:78418219
|
C | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(223): Show | 241 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.1552-1327C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418219 | ||||||
| chr17:78418274
|
CAT | C | 9 | a0001c0001t0001g0281a0001c0002t0001g0070a0001c0002t0001g0084others(6): Show | 9 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-1271_1552-127 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418274 | ||||||
| chr17:78418304
|
G | A | 317 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(314): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1552-1242G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418304 | ||||||
| chr17:78418313
|
C | G | 3 | a0001c0001t0003g0331a0001c0001t0003g0332a0001c0001t0003g0341 | 3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1552-1233C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418313 | ||||||
| chr17:78418332
|
A | G | 1 | a0001c0002t0003g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1552-1214A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418332 | ||||||
| chr17:78418361
|
C | T | 376 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(373): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1552-1185C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418361 | ||||||
| chr17:78418433
|
A | C | 1 | a0001c0001t0002g0330 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1552-1113A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418433 | ||||||
| chr17:78418605
|
G | A | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1552-941G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418605 | ||||||
| chr17:78418761
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1552-785C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418761 | ||||||
| chr17:78418806
|
C | T | 1 | a0001c0010t0001g0227 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1552-740C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418806 | ||||||
| chr17:78418861
|
CTG | C | 9 | a0001c0001t0009g0368a0001c0001t0010g0352a0001c0002t0001g0058others(6): Show | 9 | HG00408.hp1 HG02523.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-681_1552-680d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78418861 | |||||
| chr17:78419072
|
G | C | 45 | a0001c0001t0001g0283a0001c0001t0002g0014a0001c0001t0002g0263others(42): Show | 46 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552-474G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419072 | ||||||
| chr17:78419074
|
A | G | 45 | a0001c0001t0001g0283a0001c0001t0002g0014a0001c0001t0002g0263others(42): Show | 46 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552-472A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419074 | ||||||
| chr17:78419129
|
T | C | 1 | a0001c0002t0001g0035 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1552-417T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419129 | ||||||
| chr17:78419134
|
A | G | 45 | a0001c0001t0001g0283a0001c0001t0002g0014a0001c0001t0002g0263others(42): Show | 46 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552-412A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419134 | ||||||
| chr17:78419249
|
G | A | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1552-297G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419249 | ||||||
| chr17:78419439
|
G | C | 4 | a0001c0002t0001g0140a0001c0002t0001g0186a0001c0003t0008g0016others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-107G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419439 | ||||||
| chr17:78419510
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1552-36G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419510 | ||||||
| chr17:78419890
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.*10+215C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78419890 | ||||||
| chr17:78419923
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*10+248C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78419923 | ||||||
| chr17:78419964
|
A | G | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*10+289A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78419964 | ||||||
| chr17:78420117
|
C | T | 1 | a0001c0002t0001g0038 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*10+442C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420117 | ||||||
| chr17:78420179
|
G | T | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*10+504G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420179 | ||||||
| chr17:78420220
|
G | A | 2 | a0001c0003t0008g0016a0001c0012t0008g0188 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*10+545G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420220 | ||||||
| chr17:78420236
|
G | A | 1 | a0001c0001t0001g0356 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*10+561G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420236 | ||||||
| chr17:78420251
|
G | A | 3 | a0001c0001t0003g0331a0001c0001t0003g0332a0001c0001t0003g0341 | 3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.*10+576G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420251 | ||||||
| chr17:78420329
|
C | T | 1 | a0001c0002t0001g0033 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.*10+654C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420329 | ||||||
| chr17:78420331
|
T | TGGACTGT others(5): Show |
2 | a0001c0001t0009g0368a0001c0001t0010g0352 | 2 | NA18939.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.*10+657_*10+668dup others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78420331 | |||||
| chr17:78420356
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0253 | 2 | NA18959.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.*10+681C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420356 | ||||||
| chr17:78420460
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0217a0001c0001t0001g0228others(7): Show | 11 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.*10+785C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420460 | ||||||
| chr17:78420476
|
T | C | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.*10+801T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420476 | ||||||
| chr17:78420512
|
A | C | 2 | a0001c0002t0001g0140a0001c0002t0001g0186 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.*10+837A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420512 | ||||||
| chr17:78420516
|
CTGGGCCT others(9): Show |
C | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*10+842_*10+857del others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420516 | ||||||
| chr17:78420526
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.*10+851G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420526 | ||||||
| chr17:78420677
|
A | G | 1 | a0001c0002t0003g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*10+1002A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420677 | ||||||
| chr17:78420722
|
C | A | 1 | a0001c0001t0001g0317 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.*10+1047C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420722 | ||||||
| chr17:78420744
|
G | A | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*10+1069G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420744 | ||||||
| chr17:78420847
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*10+1172G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420847 | ||||||
| chr17:78420859
|
A | G | 11 | a0001c0001t0002g0345a0001c0003t0002g0176a0001c0003t0002g0177others(8): Show | 11 | HG02055.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.*10+1184A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420859 | ||||||
| chr17:78420970
|
A | AATGGTGT others(8): Show |
1 | a0001c0001t0004g0357 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*10+1296_*10+1310d others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78420970 | |||||
| chr17:78421098
|
T | A | 3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | HG02145.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*10+1423T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421098 | ||||||
| chr17:78421270
|
CAG | C | 27 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(24): Show | 28 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.*10+1601_*10+1602d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421270 | |||||
| chr17:78421273
|
A | G | 1 | a0001c0002t0002g0073 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*10+1598A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421273 | ||||||
| chr17:78421275
|
A | G | 2 | a0001c0001t0002g0270a0001c0011t0002g0315 | 2 | HG01256.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*10+1600A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421275 | ||||||
| chr17:78421286
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.*10+1611G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421286 | ||||||
| chr17:78421403
|
T | TGTCA | 360 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(357): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.*10+1729_*10+1732d others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421403 | |||||
| chr17:78421435
|
A | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(369): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.*10+1760A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421435 | ||||||
| chr17:78421436
|
G | T | 1 | a0001c0001t0001g0353 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*10+1761G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421436 | ||||||
| chr17:78421518
|
C | T | 2 | a0001c0002t0001g0072a0001c0002t0001g0081 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.*10+1843C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421518 | ||||||
| chr17:78421567
|
C | T | 1 | a0001c0002t0001g0051 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.*10+1892C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421567 | ||||||
| chr17:78421611
|
A | G | 1 | a0001c0002t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*10+1936A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421611 | ||||||
| chr17:78421674
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*10+1999C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421674 | ||||||
| chr17:78421690
|
C | CATTCCTC others(3): Show |
1 | a0002c0004t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*10+2020_*10+2029d others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421690 | |||||
| chr17:78421782
|
A | ACTG | 3 | a0001c0002t0001g0007a0001c0002t0001g0041a0001c0002t0001g0127 | 4 | HG00609.hp2 HG00639.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.*10+2110_*10+2112d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421782 | |||||
| chr17:78421802
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(310): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.*10+2127T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421802 | ||||||
| chr17:78421898
|
A | AGCGGGCG | 4 | a0001c0001t0001g0223a0001c0001t0001g0286a0001c0002t0007g0015others(1): Show | 4 | HG00733.hp1 HG01109.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.*11-2151_*11-2145d others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421898 | |||||
| chr17:78421898
|
AGCGGGCG | A | 47 | a0001c0001t0001g0219a0001c0001t0001g0242a0001c0001t0001g0262others(44): Show | 49 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.*11-2151_*11-2145d others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421898 | |||||
| chr17:78421905
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.*11-2156G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421905 | ||||||
| chr17:78421912
|
G | C | 1 | a0001c0001t0001g0287 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.*11-2149G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421912 | ||||||
| chr17:78421915
|
G | A | 14 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(11): Show | 14 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.*11-2146G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421915 | ||||||
| chr17:78421918
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.*11-2143C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421918 | ||||||
| chr17:78421919
|
G | A | 13 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(10): Show | 13 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.*11-2142G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421919 | ||||||
| chr17:78421932
|
C | T | 2 | a0001c0001t0003g0331a0001c0001t0003g0332 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.*11-2129C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421932 | ||||||
| chr17:78421957
|
C | T | 5 | a0001c0001t0001g0343a0001c0001t0001g0373a0001c0001t0001g0374others(2): Show | 5 | HG03516.hp1 NA18939.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.*11-2104C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421957 | ||||||
| chr17:78421969
|
CCT | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(278): Show | 298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.*11-2091_*11-2090d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421969 | ||||||
| chr17:78421993
|
C | T | 3 | a0001c0001t0005g0342a0001c0002t0005g0075a0001c0002t0005g0082 | 3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*11-2068C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421993 | ||||||
| chr17:78422228
|
A | T | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*11-1833A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422228 | ||||||
| chr17:78422333
|
C | T | 2 | a0001c0001t0001g0364a0001c0001t0001g0365 | 2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.*11-1728C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422333 | ||||||
| chr17:78422349
|
C | T | 4 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0001t0001g0375others(1): Show | 4 | NA18939.hp2 NA18984.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.*11-1712C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422349 | ||||||
| chr17:78422382
|
T | G | 9 | a0001c0001t0001g0281a0001c0002t0001g0070a0001c0002t0001g0084others(6): Show | 9 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.*11-1679T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422382 | ||||||
| chr17:78422421
|
G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0311 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.*11-1640G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422421 | ||||||
| chr17:78422469
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.*11-1592C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422469 | ||||||
| chr17:78422487
|
A | ATGGGTGT others(43): Show |
24 | a0001c0001t0002g0263a0001c0001t0002g0270a0001c0001t0002g0370others(21): Show | 24 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.*11-1573_*11-1524d others(52): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78422487 | |||||
| chr17:78422605
|
C | T | 4 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0349others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.*11-1456C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422605 | ||||||
| chr17:78422617
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0247a0001c0001t0001g0285others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.*11-1444C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422617 | ||||||
| chr17:78422659
|
G | A | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-1402G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422659 | ||||||
| chr17:78422726
|
C | CTGGGCTC others(7): Show |
3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | HG02145.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*11-1334_*11-1321d others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78422726 | |||||
| chr17:78422747
|
G | A | 2 | a0001c0003t0008g0016a0001c0012t0008g0188 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*11-1314G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422747 | ||||||
| chr17:78422763
|
CGT | C | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*11-1296_*11-1295d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78422763 | |||||
| chr17:78422779
|
G | A | 9 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.*11-1282G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422779 | ||||||
| chr17:78422790
|
CTTTGAAG others(10): Show |
C | 2 | a0001c0002t0007g0015a0001c0002t0007g0110 | 2 | HG01109.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.*11-1270_*11-1254d others(19): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422790 | ||||||
| chr17:78422856
|
G | A | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.*11-1205G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422856 | ||||||
| chr17:78422857
|
A | G | 1 | a0001c0001t0009g0368 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.*11-1204A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422857 | ||||||
| chr17:78422883
|
G | A | 3 | a0001c0002t0002g0112a0001c0002t0002g0189a0001c0002t0002g0196 | 3 | HG01891.hp2 HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.*11-1178G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422883 | ||||||
| chr17:78422929
|
C | T | 5 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0206others(2): Show | 5 | HG00558.hp2 HG02129.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.*11-1132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422929 | ||||||
| chr17:78422972
|
T | C | 1 | a0001c0002t0002g0065 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.*11-1089T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422972 | ||||||
| chr17:78422995
|
T | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(281): Show | 301 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.*11-1066T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422995 | ||||||
| chr17:78423011
|
G | A | 2 | a0001c0002t0007g0015a0001c0002t0007g0110 | 2 | HG01109.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.*11-1050G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423011 | ||||||
| chr17:78423055
|
G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*11-1006G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423055 | ||||||
| chr17:78423089
|
ACT | A | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-968_*11-967del others(2): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78423089 | |||||
| chr17:78423104
|
C | T | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-957C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423104 | ||||||
| chr17:78423105
|
G | GA | 276 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(273): Show | 293 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.*11-942dupA | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78423105 | |||||
| chr17:78423106
|
A | G | 24 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(21): Show | 25 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.*11-955A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423106 | ||||||
| chr17:78423119
|
AT | A | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-941delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423119 | ||||||
| chr17:78423129
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*11-932T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423129 | ||||||
| chr17:78423136
|
G | C | 3 | a0001c0001t0005g0342a0001c0002t0005g0075a0001c0002t0005g0082 | 3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*11-925G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423136 | ||||||
| chr17:78423146
|
G | A | 4 | a0001c0002t0001g0140a0001c0003t0008g0016a0001c0012t0008g0188others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.*11-915G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423146 | ||||||
| chr17:78423170
|
G | A | 6 | a0001c0002t0001g0084a0001c0002t0001g0192a0002c0004t0001g0190others(3): Show | 6 | HG01261.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*11-891G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423170 | ||||||
| chr17:78423204
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0299 | 2 | NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.*11-857T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423204 | ||||||
| chr17:78423260
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*11-801C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423260 | ||||||
| chr17:78423275
|
C | G | 211 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(208): Show | 220 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.*11-786C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423275 | ||||||
| chr17:78423345
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0102 | 2 | NA18967.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.*11-716G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423345 | ||||||
| chr17:78423364
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*11-697C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423364 | ||||||
| chr17:78423398
|
A | G | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-663A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423398 | ||||||
| chr17:78423518
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0280 | 2 | NA19054.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.*11-543A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423518 | ||||||
| chr17:78423548
|
A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0052 | 2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.*11-513A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423548 | ||||||
| chr17:78423556
|
T | C | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-505T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423556 | ||||||
| chr17:78423570
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.*11-491C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423570 | ||||||
| chr17:78423704
|
C | G | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*11-357C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423704 | ||||||
| chr17:78423801
|
G | A | 44 | a0001c0001t0002g0014a0001c0001t0002g0263a0001c0001t0002g0270others(41): Show | 45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-260G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423801 | ||||||
| chr17:78423993
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*11-68G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423993 | ||||||
| chr17:78424004
|
T | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0266a0001c0001t0001g0326others(15): Show | 18 | HG00609.hp1 HG00673.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.*11-57T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78424004 |