Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5627 |
|---|---|
| ensemblid | ENSG00000184500.16 |
| hgncid | 9456 |
| symbol | PROS1 |
| name | protein S |
| refseq_nuc | NM_000313.4 |
| refseq_prot | NP_000304.2 |
| ensembl_nuc | ENST00000394236.9 |
| ensembl_prot | ENSP00000377783.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 93873051 |
| end | 93973896 |
| strand | - |
| ver | v1.2 |
| region | chr3:93873051-93973896 |
| region5000 | chr3:93868051-93978896 |
| regionname0 | PROS1_chr3_93873051_93973896 |
| regionname5000 | PROS1_chr3_93868051_93978896 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 676 | 302 | 90 | 61 | 107 | 12 | 30 | 83 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0002 | 0/0 | 676 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0003 | 0/0 | 676 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0004 | 0/0 | 676 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0005 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0006 | 0/0 | 676 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0007 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0008 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0009 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2031 | 207 | 79 | 39 | 58 | 8 | 21 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0002 | 0/0 | 2031 | 91 | 10 | 22 | 47 | 4 | 8 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0003 | 0/0 | 2031 | 3 | 0 | 0 | 0 | 0 | 3 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0004 | 0/0 | 2031 | 3 | 3 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0005 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0006 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0007 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0008 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0009 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0010 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0011 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0012 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0013 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| c0014 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1342 | 236 | 55 | 51 | 91 | 10 | 28 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0002 | 1/0 | 1342 | 64 | 28 | 9 | 18 | 2 | 6 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0003 | 0/0 | 1342 | 6 | 5 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0004 | 0/0 | 1342 | 2 | 2 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0005 | 0/0 | 1342 | 2 | 0 | 1 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0006 | 0/0 | 1342 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0007 | 0/0 | 1342 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0008 | 0/0 | 1342 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| t0009 | 0/0 | 1342 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2031 | 207 | 79 | 39 | 58 | 8 | 21 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0002 | 0/0 | 2031 | 91 | 10 | 22 | 47 | 4 | 8 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0007 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0009 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0010 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0013 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0002c0004 | 0/0 | 2031 | 3 | 3 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0003c0003 | 0/0 | 2031 | 3 | 0 | 0 | 0 | 0 | 3 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0004c0014 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0005c0012 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0006c0008 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0007c0006 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0008c0011 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0009c0005 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3372 | 132 | 40 | 28 | 42 | 6 | 15 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0002 | 1/0 | 3372 | 61 | 28 | 9 | 15 | 2 | 6 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0003 | 0/0 | 3372 | 6 | 5 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0004 | 0/0 | 3372 | 2 | 2 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0005 | 0/0 | 3372 | 2 | 0 | 1 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0006 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0007 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0008 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0001t0009 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0002t0001 | 0/0 | 3372 | 91 | 10 | 22 | 47 | 4 | 8 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0007t0002 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0009t0001 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0010t0001 | 0/0 | 3372 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0001c0013t0002 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0002c0004t0001 | 0/0 | 3372 | 3 | 3 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0003c0003t0001 | 0/0 | 3372 | 3 | 0 | 0 | 0 | 0 | 3 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0004c0014t0001 | 0/0 | 3372 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0005c0012t0001 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0006c0008t0001 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0007c0006t0001 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0008c0011t0001 | 0/0 | 3372 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| a0009c0005t0002 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | copy fasta | chr3 | 93868051 | 93978896 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0007g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0007t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0009t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0010t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0001c0013t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0002c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0002c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0002c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0004c0014t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0005c0012t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0006c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0007c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0008c0011t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| a0009c0005t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0297 | EUR | GBR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | FIN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00639 | hp2 | a0004 | c0014 | t0001 | g0088 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0289 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0230 | EUR | IBS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0154 | EUR | IBS | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CDX | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02257 | hp2 | a0006 | c0008 | t0001 | g0176 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0184 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0183 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0219 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0305 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03834 | hp1 | a0001 | c0010 | t0001 | g0293 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0210 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04184 | hp1 | a0008 | c0011 | t0001 | g0199 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0209 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0249 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | STU | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | YRI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | CHB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0155 | AFR | YRI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | YRI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18939 | hp2 | a0009 | c0005 | t0002 | g0172 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18943 | hp1 | a0007 | c0006 | t0001 | g0262 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18956 | hp1 | a0001 | c0013 | t0002 | g0310 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19010 | hp1 | a0005 | c0012 | t0001 | g0292 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | LWK | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0129 | AFR | LWK | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19067 | hp1 | a0001 | c0007 | t0002 | g0311 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | YRI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | ASW | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ASW | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0079 | EUR | TSI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | TSI | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | GIH | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | GIH | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| HG06807 | hp2 | a0001 | c0009 | t0001 | g0139 | AFR | USA | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | USA | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0022 | REF | REF | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0101 | REF | REF | PROS1_chr3_93868051_93978896 | PROS1 | chr3 | 93868051 | 93978896 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93879279
|
C | T | 1 | a0006 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1528G>A | p.Val510Met | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/15 | 1675/3372 | 1528/2031 | 510/676 | chr3 | 93879279 | ||
| chr3:93884827
|
C | T | 1 | a0007 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.1393G>A | p.Glu465Lys | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/15 | 1540/3372 | 1393/2031 | 465/676 | chr3 | 93884827 | ||
| chr3:93900821
|
T | G | 1 | a0008 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.710A>C | p.Lys237Thr | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/15 | 857/3372 | 710/2031 | 237/676 | chr3 | 93900821 | ||
| chr3:93900833
|
C | T | 1 | a0003 | 3 | HG03942.hp1 HG04199.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.698G>A | p.Arg233Lys | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/15 | 845/3372 | 698/2031 | 233/676 | chr3 | 93900833 | ||
| chr3:93905799
|
T | C | 1 | a0005 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.586A>G | p.Lys196Glu | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/15 | 733/3372 | 586/2031 | 196/676 | chr3 | 93905799 | ||
| chr3:93927257
|
G | A | 1 | a0004 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.227C>T | p.Pro76Leu | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/15 | 374/3372 | 227/2031 | 76/676 | chr3 | 93927257 | ||
| chr3:93927365
|
C | A | 1 | a0002 | 3 | HG02280.hp2 HG02965.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.119G>T | p.Arg40Leu | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/15 | 266/3372 | 119/2031 | 40/676 | chr3 | 93927365 | ||
| chr3:93927390
|
C | T | 1 | a0009 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.94G>A | p.Ala32Thr | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/15 | 241/3372 | 94/2031 | 32/676 | chr3 | 93927390 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93874275
|
T | C | 4 | a0001c0002a0003c0003a0007c0006others(1): Show | 96 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(93): Show |
synonymous_variant | LOW | c.2001A>G | p.Pro667Pro | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 2148/3372 | 2001/2031 | 667/676 | chr3 | 93874275 | ||
| chr3:93879313
|
A | G | 2 | a0001c0007a0001c0013 | 2 | NA18956.hp1 NA19067.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1494T>C | p.Asn498Asn | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/15 | 1641/3372 | 1494/2031 | 498/676 | chr3 | 93879313 | ||
| chr3:93893056
|
G | A | 2 | a0001c0009a0002c0004 | 4 | HG02280.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.1032C>T | p.Ile344Ile | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/15 | 1179/3372 | 1032/2031 | 344/676 | chr3 | 93893056 | ||
| chr3:93896578
|
G | A | 1 | a0001c0010 | 1 | HG03834.hp1 | splice_region_variant&synonymous_variant | LOW | c.963C>T | p.Ser321Ser | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/15 | 1110/3372 | 963/2031 | 321/676 | chr3 | 93896578 | ||
| chr3:93905905
|
T | C | 1 | a0001c0013 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.480A>G | p.Glu160Glu | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/15 | 627/3372 | 480/2031 | 160/676 | chr3 | 93905905 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93873253
|
A | C | 1 | a0001c0001t0008 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 992 | chr3 | 93873253 | |||||
| chr3:93873725
|
T | G | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(14): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*520A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 520 | chr3 | 93873725 | |||||
| chr3:93873791
|
C | T | 1 | a0001c0001t0007 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 454 | chr3 | 93873791 | |||||
| chr3:93873865
|
T | A | 1 | a0001c0001t0005 | 2 | HG01346.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 380 | chr3 | 93873865 | |||||
| chr3:93873875
|
C | T | 1 | a0001c0001t0006 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 370 | chr3 | 93873875 | |||||
| chr3:93874048
|
G | A | 1 | a0001c0001t0003 | 6 | HG01975.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*197C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 197 | chr3 | 93874048 | |||||
| chr3:93874108
|
G | A | 1 | a0001c0001t0009 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 15/15 | 137 | chr3 | 93874108 | |||||
| chr3:93973811
|
A | C | 1 | a0001c0001t0004 | 2 | HG02896.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-62T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/15 | 62 | chr3 | 93973811 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93874668
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01952.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1871-263C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93874668 | ||||||
| chr3:93874927
|
C | T | 3 | a0001c0001t0002g0115a0001c0001t0002g0118a0001c0001t0002g0229 | 3 | HG02083.hp2 HG02165.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1871-522G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93874927 | ||||||
| chr3:93875039
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1871-634T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875039 | ||||||
| chr3:93875564
|
G | C | 1 | a0001c0001t0002g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1871-1159C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875564 | ||||||
| chr3:93875621
|
TACCTC | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0220 | 3 | HG02486.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1871-1221_1871-121 others(9): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875621 | ||||||
| chr3:93875624
|
C | CTCTA | 4 | a0001c0001t0002g0156a0001c0002t0001g0180a0001c0002t0001g0277others(1): Show | 4 | HG02630.hp2 HG03942.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1871-1223_1871-122 others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875624 | ||||||
| chr3:93875624
|
CTCTA | C | 113 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(110): Show | 114 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1871-1223_1871-122 others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875624 | ||||||
| chr3:93875624
|
CTCTATCT others(1): Show |
C | 107 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(104): Show | 108 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1871-1227_1871-122 others(12): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875624 | ||||||
| chr3:93875624
|
CTCTATCT others(5): Show |
C | 26 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(23): Show | 26 | HG00642.hp2 HG01099.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1871-1231_1871-122 others(16): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875624 | ||||||
| chr3:93875624
|
CTCTATCT others(9): Show |
C | 21 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0138others(18): Show | 21 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1871-1235_1871-122 others(20): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875624 | ||||||
| chr3:93875629
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0220 | 3 | HG02486.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1871-1224A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875629 | ||||||
| chr3:93875630
|
CTA | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0220 | 3 | HG02486.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1871-1227_1871-122 others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875630 | ||||||
| chr3:93875663
|
TATCTATC others(8): Show |
T | 2 | a0001c0001t0001g0023a0001c0001t0001g0081 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1871-1273_1871-125 others(19): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875663 | ||||||
| chr3:93875762
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1870+1204A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875762 | ||||||
| chr3:93875789
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1870+1177T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93875789 | ||||||
| chr3:93876309
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1870+657T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876309 | ||||||
| chr3:93876310
|
C | G | 1 | a0001c0001t0002g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1870+656G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876310 | ||||||
| chr3:93876444
|
C | A | 1 | a0001c0001t0007g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1870+522G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876444 | ||||||
| chr3:93876445
|
C | T | 1 | a0001c0001t0007g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1870+521G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876445 | ||||||
| chr3:93876457
|
C | T | 25 | a0001c0001t0001g0036a0001c0001t0001g0105a0001c0001t0001g0135others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1870+509G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876457 | ||||||
| chr3:93876588
|
C | CA | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 121 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1870+377dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876588 | ||||||
| chr3:93876588
|
C | CAA | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0018others(19): Show | 22 | HG01261.hp2 HG01358.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1870+376_1870+377d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876588 | ||||||
| chr3:93876588
|
CA | C | 24 | a0001c0001t0001g0036a0001c0001t0001g0148a0001c0001t0001g0149others(21): Show | 24 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1870+377delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876588 | ||||||
| chr3:93876771
|
T | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01952.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1870+195A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 14/14 | chr3 | 93876771 | ||||||
| chr3:93877636
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1645-445G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93877636 | ||||||
| chr3:93877705
|
C | T | 3 | a0001c0002t0001g0054a0001c0002t0001g0131a0001c0002t0001g0188 | 3 | HG01884.hp2 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1645-514G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93877705 | ||||||
| chr3:93877711
|
C | T | 2 | a0001c0001t0001g0084a0004c0014t0001g0088 | 2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1645-520G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93877711 | ||||||
| chr3:93877783
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1645-592C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93877783 | ||||||
| chr3:93878063
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1645-872T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878063 | ||||||
| chr3:93878131
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1645-940A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878131 | ||||||
| chr3:93878256
|
AAAGCTCC others(21): Show |
A | 1 | a0001c0013t0002g0310 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644+879_1644+906d others(30): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878256 | ||||||
| chr3:93878470
|
C | A | 1 | a0001c0001t0003g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1644+693G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878470 | ||||||
| chr3:93878495
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1644+668G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878495 | ||||||
| chr3:93878585
|
C | A | 7 | a0001c0002t0001g0112a0001c0002t0001g0175a0001c0002t0001g0215others(4): Show | 7 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1644+578G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878585 | ||||||
| chr3:93878823
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1644+340T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93878823 | ||||||
| chr3:93879047
|
T | C | 1 | a0001c0002t0001g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1644+116A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93879047 | ||||||
| chr3:93879091
|
A | AAATAC | 8 | a0001c0002t0001g0112a0001c0002t0001g0175a0001c0002t0001g0215others(5): Show | 8 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+67_1644+71dup others(5): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 13/14 | chr3 | 93879091 | ||||||
| chr3:93879513
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1493-199C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93879513 | ||||||
| chr3:93879586
|
TTGCTCTT others(6): Show |
T | 4 | a0001c0001t0001g0138a0001c0001t0001g0306a0001c0001t0007g0305others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1493-285_1493-273d others(15): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93879586 | ||||||
| chr3:93879667
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1493-353A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93879667 | ||||||
| chr3:93879968
|
C | T | 1 | a0001c0002t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1493-654G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93879968 | ||||||
| chr3:93880061
|
T | G | 1 | a0001c0001t0002g0093 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1493-747A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93880061 | ||||||
| chr3:93880301
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1493-987G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93880301 | ||||||
| chr3:93880586
|
G | A | 1 | a0001c0013t0002g0310 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1493-1272C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93880586 | ||||||
| chr3:93880847
|
T | A | 1 | a0001c0013t0002g0310 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1493-1533A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93880847 | ||||||
| chr3:93881369
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1493-2055C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881369 | ||||||
| chr3:93881385
|
G | T | 1 | a0001c0013t0002g0310 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1493-2071C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881385 | ||||||
| chr3:93881556
|
C | CT | 161 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0053others(158): Show | 162 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1493-2243dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881556 | ||||||
| chr3:93881556
|
C | CTT | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 70 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1493-2244_1493-224 others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881556 | ||||||
| chr3:93881556
|
C | CTTT | 10 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0046others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1493-2245_1493-224 others(7): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881556 | ||||||
| chr3:93881726
|
A | T | 1 | a0001c0002t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1493-2412T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881726 | ||||||
| chr3:93881864
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1493-2550C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93881864 | ||||||
| chr3:93882052
|
G | A | 8 | a0001c0001t0001g0200a0001c0001t0001g0307a0001c0001t0004g0004others(5): Show | 8 | HG02280.hp2 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1492+2676C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882052 | ||||||
| chr3:93882186
|
T | A | 1 | a0001c0002t0001g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1492+2542A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882186 | ||||||
| chr3:93882516
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1492+2212G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882516 | ||||||
| chr3:93882620
|
T | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1492+2108A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882620 | ||||||
| chr3:93882714
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 64 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1492+2014G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882714 | ||||||
| chr3:93882720
|
C | A | 1 | a0001c0002t0001g0237 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1492+2008G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882720 | ||||||
| chr3:93882955
|
A | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(90): Show | 94 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1492+1773T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93882955 | ||||||
| chr3:93883455
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1492+1273T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93883455 | ||||||
| chr3:93884347
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1492+381G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93884347 | ||||||
| chr3:93884431
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1492+297G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93884431 | ||||||
| chr3:93884593
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1492+135T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 12/14 | chr3 | 93884593 | ||||||
| chr3:93884924
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324-28C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 11/14 | chr3 | 93884924 | ||||||
| chr3:93884964
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0136 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1324-68C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 11/14 | chr3 | 93884964 | ||||||
| chr3:93885472
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1324-576G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 11/14 | chr3 | 93885472 | ||||||
| chr3:93885627
|
G | C | 1 | a0001c0002t0001g0251 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1323+709C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 11/14 | chr3 | 93885627 | ||||||
| chr3:93885838
|
C | T | 8 | a0001c0001t0001g0200a0001c0001t0001g0307a0001c0001t0004g0004others(5): Show | 8 | HG02280.hp2 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1323+498G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 11/14 | chr3 | 93885838 | ||||||
| chr3:93886282
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 54 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1323+54T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 11/14 | chr3 | 93886282 | ||||||
| chr3:93886657
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1156-154A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93886657 | ||||||
| chr3:93886727
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1156-224T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93886727 | ||||||
| chr3:93886895
|
T | C | 25 | a0001c0001t0001g0036a0001c0001t0001g0105a0001c0001t0001g0142others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1156-392A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93886895 | ||||||
| chr3:93886910
|
C | CT | 33 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0273others(30): Show | 33 | HG00408.hp2 HG01243.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.1156-408dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93886910 | ||||||
| chr3:93886942
|
C | T | 1 | a0001c0002t0001g0260 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1156-439G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93886942 | ||||||
| chr3:93886996
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1156-493C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93886996 | ||||||
| chr3:93887000
|
G | A | 1 | a0001c0002t0001g0178 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1156-497C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887000 | ||||||
| chr3:93887076
|
G | A | 1 | a0001c0002t0001g0211 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1156-573C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887076 | ||||||
| chr3:93887080
|
G | A | 4 | a0001c0001t0002g0151a0001c0001t0002g0192a0001c0001t0002g0193others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-577C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887080 | ||||||
| chr3:93887209
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1156-706G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887209 | ||||||
| chr3:93887250
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1156-747T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887250 | ||||||
| chr3:93887411
|
A | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1156-908T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887411 | ||||||
| chr3:93887549
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1156-1046C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887549 | ||||||
| chr3:93887638
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1156-1135T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887638 | ||||||
| chr3:93887759
|
G | C | 1 | a0001c0002t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1156-1256C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887759 | ||||||
| chr3:93887843
|
C | A | 1 | a0001c0001t0007g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1156-1340G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93887843 | ||||||
| chr3:93888062
|
T | G | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1156-1559A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93888062 | ||||||
| chr3:93888790
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1156-2287T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93888790 | ||||||
| chr3:93889274
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1156-2771G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93889274 | ||||||
| chr3:93889314
|
T | A | 3 | a0001c0001t0002g0085a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG01258.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1156-2811A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93889314 | ||||||
| chr3:93889780
|
A | T | 1 | a0001c0001t0001g0291 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1155+3153T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93889780 | ||||||
| chr3:93890001
|
G | A | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1155+2932C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890001 | ||||||
| chr3:93890096
|
C | T | 1 | a0004c0014t0001g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1155+2837G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890096 | ||||||
| chr3:93890515
|
C | T | 7 | a0001c0002t0001g0263a0001c0002t0001g0265a0001c0002t0001g0266others(4): Show | 7 | NA18612.hp2 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155+2418G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890515 | ||||||
| chr3:93890537
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1155+2396G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890537 | ||||||
| chr3:93890615
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 54 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1155+2318G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890615 | ||||||
| chr3:93890699
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1155+2234G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890699 | ||||||
| chr3:93890819
|
T | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0102a0001c0001t0002g0104 | 3 | HG00438.hp1 HG02080.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1155+2114A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93890819 | ||||||
| chr3:93891351
|
T | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 64 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1155+1582A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93891351 | ||||||
| chr3:93891513
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1155+1420G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93891513 | ||||||
| chr3:93891606
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1155+1327G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93891606 | ||||||
| chr3:93891771
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0007g0305 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1155+1162T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93891771 | ||||||
| chr3:93891846
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1155+1087A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93891846 | ||||||
| chr3:93892052
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1155+881C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892052 | ||||||
| chr3:93892223
|
A | G | 1 | a0006c0008t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1155+710T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892223 | ||||||
| chr3:93892292
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1155+641C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892292 | ||||||
| chr3:93892398
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1155+535C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892398 | ||||||
| chr3:93892480
|
C | T | 37 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(34): Show | 37 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.1155+453G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892480 | ||||||
| chr3:93892482
|
G | GATTCTAC others(52): Show |
1 | a0001c0002t0001g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1155+450_1155+451i others(61): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892482 | ||||||
| chr3:93892483
|
G | A | 1 | a0001c0002t0001g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1155+450C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892483 | ||||||
| chr3:93892485
|
A | C | 1 | a0001c0002t0001g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1155+448T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892485 | ||||||
| chr3:93892624
|
C | CA | 7 | a0001c0001t0001g0035a0001c0001t0001g0138a0001c0001t0001g0301others(4): Show | 7 | HG01192.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155+308dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 10/14 | chr3 | 93892624 | ||||||
| chr3:93893369
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.966-247T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93893369 | ||||||
| chr3:93893525
|
T | C | 6 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.966-403A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93893525 | ||||||
| chr3:93894187
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.966-1065C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894187 | ||||||
| chr3:93894250
|
A | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.966-1128T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894250 | ||||||
| chr3:93894356
|
T | A | 1 | a0001c0002t0001g0178 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.966-1234A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894356 | ||||||
| chr3:93894473
|
A | G | 4 | a0001c0001t0002g0087a0001c0001t0002g0117a0001c0001t0002g0124others(1): Show | 4 | HG01106.hp1 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.966-1351T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894473 | ||||||
| chr3:93894843
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.966-1721C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894843 | ||||||
| chr3:93894924
|
C | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.965+1652G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894924 | ||||||
| chr3:93894954
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.965+1622C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93894954 | ||||||
| chr3:93895084
|
C | T | 2 | a0002c0004t0001g0184a0003c0003t0001g0210 | 2 | HG02280.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.965+1492G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895084 | ||||||
| chr3:93895098
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.965+1478A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895098 | ||||||
| chr3:93895226
|
G | A | 5 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0177others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.965+1350C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895226 | ||||||
| chr3:93895263
|
T | G | 1 | a0001c0002t0001g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.965+1313A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895263 | ||||||
| chr3:93895639
|
A | T | 1 | a0001c0001t0002g0102 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.965+937T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895639 | ||||||
| chr3:93895772
|
C | A | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG01975.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.965+804G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895772 | ||||||
| chr3:93895920
|
C | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01952.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.965+656G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93895920 | ||||||
| chr3:93896043
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.965+533T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93896043 | ||||||
| chr3:93896358
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.965+218C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93896358 | ||||||
| chr3:93896510
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.965+66G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 9/14 | chr3 | 93896510 | ||||||
| chr3:93896808
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.850-117G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 8/14 | chr3 | 93896808 | ||||||
| chr3:93897350
|
TATTG | T | 23 | a0001c0001t0001g0036a0001c0001t0001g0105a0001c0001t0001g0135others(20): Show | 23 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.850-663_850-660del others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 8/14 | chr3 | 93897350 | ||||||
| chr3:93897357
|
C | A | 23 | a0001c0001t0001g0036a0001c0001t0001g0105a0001c0001t0001g0135others(20): Show | 23 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.850-666G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 8/14 | chr3 | 93897357 | ||||||
| chr3:93897578
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.849+870T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 8/14 | chr3 | 93897578 | ||||||
| chr3:93897964
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.849+484A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 8/14 | chr3 | 93897964 | ||||||
| chr3:93898015
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.849+433G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 8/14 | chr3 | 93898015 | ||||||
| chr3:93898746
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.728-177G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93898746 | ||||||
| chr3:93898797
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.728-228A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93898797 | ||||||
| chr3:93898938
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.728-369G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93898938 | ||||||
| chr3:93899111
|
G | A | 1 | a0001c0002t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.728-542C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899111 | ||||||
| chr3:93899150
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.728-581A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899150 | ||||||
| chr3:93899162
|
A | T | 2 | a0001c0002t0001g0211a0004c0014t0001g0088 | 2 | HG00639.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.728-593T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899162 | ||||||
| chr3:93899334
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.728-765C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899334 | ||||||
| chr3:93899336
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.728-767G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899336 | ||||||
| chr3:93899349
|
A | G | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG01975.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.728-780T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899349 | ||||||
| chr3:93899469
|
T | C | 7 | a0001c0001t0002g0229a0001c0002t0001g0175a0001c0002t0001g0215others(4): Show | 7 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.728-900A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899469 | ||||||
| chr3:93899488
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.728-919A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899488 | ||||||
| chr3:93899489
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.728-920T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899489 | ||||||
| chr3:93899772
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.727+1032T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899772 | ||||||
| chr3:93899941
|
G | A | 1 | a0001c0002t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.727+863C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93899941 | ||||||
| chr3:93900008
|
C | CAT | 4 | a0001c0001t0002g0111a0001c0001t0002g0145a0001c0001t0002g0164others(1): Show | 4 | HG01891.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+794_727+795dup others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93900008 | ||||||
| chr3:93900093
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.727+711G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93900093 | ||||||
| chr3:93900770
|
T | A | 1 | a0001c0002t0001g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.727+34A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 7/14 | chr3 | 93900770 | ||||||
| chr3:93901425
|
C | T | 1 | a0001c0002t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.602-496G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901425 | ||||||
| chr3:93901470
|
G | T | 3 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0167 | 3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.602-541C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901470 | ||||||
| chr3:93901583
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0291 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.602-654C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901583 | ||||||
| chr3:93901742
|
T | G | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 31 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.602-813A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901742 | ||||||
| chr3:93901816
|
T | A | 1 | a0001c0002t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.602-887A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901816 | ||||||
| chr3:93901854
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.602-925C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901854 | ||||||
| chr3:93901991
|
A | C | 2 | a0001c0002t0001g0265a0001c0002t0001g0267 | 2 | NA18612.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.602-1062T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93901991 | ||||||
| chr3:93902350
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.602-1421A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93902350 | ||||||
| chr3:93902888
|
GGTTT | G | 4 | a0001c0001t0002g0111a0001c0001t0002g0145a0001c0001t0002g0164others(1): Show | 4 | HG01891.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-1963_602-1960d others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93902888 | ||||||
| chr3:93903067
|
G | A | 2 | a0001c0001t0002g0087a0001c0002t0001g0290 | 2 | HG02886.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.602-2138C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903067 | ||||||
| chr3:93903293
|
C | A | 1 | a0001c0002t0001g0296 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.602-2364G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903293 | ||||||
| chr3:93903383
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.601+2401C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903383 | ||||||
| chr3:93903618
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.601+2166G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903618 | ||||||
| chr3:93903655
|
C | A | 1 | a0001c0002t0001g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.601+2129G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903655 | ||||||
| chr3:93903689
|
A | T | 1 | a0001c0001t0002g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601+2095T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903689 | ||||||
| chr3:93903723
|
G | A | 2 | a0001c0002t0001g0097a0001c0002t0001g0098 | 2 | NA18941.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.601+2061C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903723 | ||||||
| chr3:93903945
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601+1839G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93903945 | ||||||
| chr3:93904062
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.601+1722C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93904062 | ||||||
| chr3:93904569
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.601+1215T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93904569 | ||||||
| chr3:93904598
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG01952.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.601+1186A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93904598 | ||||||
| chr3:93904628
|
G | C | 25 | a0001c0001t0001g0036a0001c0001t0001g0105a0001c0001t0001g0135others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.601+1156C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93904628 | ||||||
| chr3:93904677
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.601+1107A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93904677 | ||||||
| chr3:93904786
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.601+998C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93904786 | ||||||
| chr3:93905017
|
G | C | 1 | a0001c0001t0002g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.601+767C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93905017 | ||||||
| chr3:93905525
|
A | G | 1 | a0001c0002t0001g0263 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.601+259T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93905525 | ||||||
| chr3:93905664
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601+120T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93905664 | ||||||
| chr3:93905741
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.601+43G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 6/14 | chr3 | 93905741 | ||||||
| chr3:93906359
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-216G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906359 | ||||||
| chr3:93906373
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.347-230G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906373 | ||||||
| chr3:93906386
|
G | A | 2 | a0001c0002t0001g0076a0001c0002t0001g0077 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.347-243C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906386 | ||||||
| chr3:93906388
|
C | T | 1 | a0001c0002t0001g0300 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.347-245G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906388 | ||||||
| chr3:93906454
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.347-311G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906454 | ||||||
| chr3:93906493
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG02615.hp2 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-350C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906493 | ||||||
| chr3:93906557
|
C | G | 8 | a0001c0001t0001g0200a0001c0001t0001g0307a0001c0001t0004g0004others(5): Show | 8 | HG02280.hp2 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-414G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906557 | ||||||
| chr3:93906676
|
A | G | 1 | a0001c0001t0006g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.347-533T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906676 | ||||||
| chr3:93906848
|
C | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-705G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906848 | ||||||
| chr3:93906885
|
C | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-742G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906885 | ||||||
| chr3:93906919
|
G | T | 80 | a0001c0001t0001g0081a0001c0001t0001g0223a0001c0001t0001g0232others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.347-776C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93906919 | ||||||
| chr3:93907102
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.347-959C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907102 | ||||||
| chr3:93907170
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.347-1027G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907170 | ||||||
| chr3:93907510
|
T | C | 1 | a0001c0002t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.347-1367A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907510 | ||||||
| chr3:93907524
|
C | A | 2 | a0001c0001t0002g0204a0001c0001t0002g0222 | 2 | HG01993.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.347-1381G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907524 | ||||||
| chr3:93907564
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.347-1421G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907564 | ||||||
| chr3:93907916
|
C | T | 1 | a0001c0002t0001g0266 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.347-1773G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907916 | ||||||
| chr3:93907918
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.347-1775A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907918 | ||||||
| chr3:93907937
|
A | T | 1 | a0001c0001t0001g0304 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.347-1794T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93907937 | ||||||
| chr3:93908003
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.347-1860G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908003 | ||||||
| chr3:93908004
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.347-1861C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908004 | ||||||
| chr3:93908009
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.347-1866C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908009 | ||||||
| chr3:93908251
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.347-2108C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908251 | ||||||
| chr3:93908329
|
A | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-2186T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908329 | ||||||
| chr3:93908435
|
G | A | 1 | a0006c0008t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346+2184C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908435 | ||||||
| chr3:93908493
|
A | C | 1 | a0001c0001t0002g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.346+2126T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908493 | ||||||
| chr3:93908968
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(272): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.346+1651C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93908968 | ||||||
| chr3:93909153
|
T | C | 1 | a0001c0002t0001g0186 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.346+1466A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909153 | ||||||
| chr3:93909433
|
T | TA | 41 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0041others(38): Show | 41 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.346+1185dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909433 | ||||||
| chr3:93909449
|
A | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+1170T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909449 | ||||||
| chr3:93909610
|
A | T | 134 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(131): Show | 135 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.346+1009T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909610 | ||||||
| chr3:93909654
|
T | C | 1 | a0001c0002t0001g0002 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.346+965A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909654 | ||||||
| chr3:93909814
|
G | GT | 33 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(30): Show | 33 | HG00558.hp1 HG00621.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.346+804dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909814 | ||||||
| chr3:93909956
|
C | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0191a0001c0001t0002g0220others(2): Show | 6 | HG02486.hp2 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+663G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909956 | ||||||
| chr3:93909957
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+662C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93909957 | ||||||
| chr3:93910363
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.346+256C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93910363 | ||||||
| chr3:93910411
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.346+208T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 4/14 | chr3 | 93910411 | ||||||
| chr3:93910794
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.260-89T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93910794 | ||||||
| chr3:93910940
|
C | T | 81 | a0001c0001t0001g0223a0001c0001t0001g0232a0001c0001t0002g0240others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.260-235G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93910940 | ||||||
| chr3:93911226
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.260-521A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93911226 | ||||||
| chr3:93911273
|
G | A | 1 | a0001c0001t0008g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.260-568C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93911273 | ||||||
| chr3:93911339
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.260-634C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93911339 | ||||||
| chr3:93911829
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.260-1124C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93911829 | ||||||
| chr3:93912116
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.260-1411C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912116 | ||||||
| chr3:93912279
|
A | T | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.260-1574T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912279 | ||||||
| chr3:93912296
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.260-1591A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912296 | ||||||
| chr3:93912444
|
A | T | 1 | a0006c0008t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.260-1739T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912444 | ||||||
| chr3:93912471
|
G | C | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.260-1766C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912471 | ||||||
| chr3:93912613
|
C | T | 3 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0288 | 3 | NA18948.hp2 NA18978.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.260-1908G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912613 | ||||||
| chr3:93912621
|
T | C | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.260-1916A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912621 | ||||||
| chr3:93912716
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.260-2011G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912716 | ||||||
| chr3:93912744
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.260-2039G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912744 | ||||||
| chr3:93912788
|
A | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.260-2083T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912788 | ||||||
| chr3:93912848
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG02615.hp2 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.260-2143G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912848 | ||||||
| chr3:93912893
|
T | C | 1 | a0001c0009t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260-2188A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93912893 | ||||||
| chr3:93913019
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.260-2314C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913019 | ||||||
| chr3:93913106
|
T | C | 2 | a0001c0001t0002g0106a0001c0001t0002g0123 | 2 | HG02300.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.260-2401A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913106 | ||||||
| chr3:93913182
|
T | C | 3 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0167 | 3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.260-2477A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913182 | ||||||
| chr3:93913249
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.260-2544A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913249 | ||||||
| chr3:93913257
|
C | G | 1 | a0009c0005t0002g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.260-2552G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913257 | ||||||
| chr3:93913341
|
C | T | 5 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0130others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-2636G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913341 | ||||||
| chr3:93913354
|
T | C | 8 | a0001c0001t0001g0200a0001c0001t0001g0307a0001c0001t0004g0004others(5): Show | 8 | HG02280.hp2 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-2649A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913354 | ||||||
| chr3:93913402
|
A | C | 1 | a0001c0001t0002g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.260-2697T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913402 | ||||||
| chr3:93913593
|
T | A | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG01346.hp1 HG02165.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-2888A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913593 | ||||||
| chr3:93913713
|
G | C | 2 | a0001c0002t0001g0137a0001c0002t0001g0226 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.260-3008C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913713 | ||||||
| chr3:93913859
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.260-3154A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913859 | ||||||
| chr3:93913880
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.260-3175T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93913880 | ||||||
| chr3:93914045
|
G | T | 81 | a0001c0001t0001g0223a0001c0001t0001g0232a0001c0001t0002g0240others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.260-3340C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914045 | ||||||
| chr3:93914108
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.260-3403A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914108 | ||||||
| chr3:93914156
|
C | T | 1 | a0001c0002t0001g0091 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.260-3451G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914156 | ||||||
| chr3:93914186
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.260-3481G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914186 | ||||||
| chr3:93914220
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.260-3515A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914220 | ||||||
| chr3:93914536
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0306a0001c0001t0007g0305others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-3831C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914536 | ||||||
| chr3:93914592
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(293): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.260-3887A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93914592 | ||||||
| chr3:93915076
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-4371C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93915076 | ||||||
| chr3:93915139
|
C | A | 2 | a0001c0001t0005g0281a0001c0001t0005g0289 | 2 | HG01346.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.260-4434G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93915139 | ||||||
| chr3:93915314
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.260-4609T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93915314 | ||||||
| chr3:93915842
|
C | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-5137G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93915842 | ||||||
| chr3:93916336
|
G | T | 1 | a0001c0002t0001g0266 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.260-5631C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93916336 | ||||||
| chr3:93916422
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.260-5717T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93916422 | ||||||
| chr3:93916918
|
A | G | 2 | a0001c0001t0002g0071a0001c0001t0002g0075 | 2 | HG01074.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.260-6213T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93916918 | ||||||
| chr3:93916919
|
A | C | 7 | a0001c0002t0001g0263a0001c0002t0001g0265a0001c0002t0001g0266others(4): Show | 7 | NA18612.hp2 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-6214T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93916919 | ||||||
| chr3:93917116
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.260-6411G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917116 | ||||||
| chr3:93917265
|
TTTTGTTT others(5): Show |
T | 37 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(34): Show | 37 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.260-6572_260-6561d others(14): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917265 | ||||||
| chr3:93917310
|
G | T | 1 | a0003c0003t0001g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.260-6605C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917310 | ||||||
| chr3:93917317
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.260-6612A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917317 | ||||||
| chr3:93917377
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.260-6672C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917377 | ||||||
| chr3:93917471
|
C | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.260-6766G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917471 | ||||||
| chr3:93917485
|
C | T | 1 | a0006c0008t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.259+6755G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917485 | ||||||
| chr3:93917532
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.259+6708T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917532 | ||||||
| chr3:93917625
|
G | C | 26 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(23): Show | 26 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.259+6615C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917625 | ||||||
| chr3:93917648
|
G | T | 1 | a0001c0002t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.259+6592C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917648 | ||||||
| chr3:93917654
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.259+6586G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917654 | ||||||
| chr3:93917675
|
C | A | 2 | a0001c0001t0001g0084a0004c0014t0001g0088 | 2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.259+6565G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917675 | ||||||
| chr3:93917687
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.259+6553C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917687 | ||||||
| chr3:93917728
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259+6512C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917728 | ||||||
| chr3:93917835
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.259+6405G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917835 | ||||||
| chr3:93917967
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.259+6273G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93917967 | ||||||
| chr3:93918009
|
C | T | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259+6231G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93918009 | ||||||
| chr3:93918134
|
T | G | 5 | a0001c0002t0001g0208a0001c0002t0001g0227a0001c0002t0001g0243others(2): Show | 5 | HG01192.hp2 HG01358.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+6106A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93918134 | ||||||
| chr3:93918233
|
C | G | 2 | a0001c0002t0001g0181a0001c0002t0001g0189 | 2 | HG00733.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.259+6007G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93918233 | ||||||
| chr3:93918485
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259+5755G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93918485 | ||||||
| chr3:93918605
|
C | T | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+5635G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93918605 | ||||||
| chr3:93918911
|
T | G | 1 | a0001c0002t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.259+5329A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93918911 | ||||||
| chr3:93919123
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.259+5117C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919123 | ||||||
| chr3:93919173
|
A | G | 97 | a0001c0001t0001g0223a0001c0001t0001g0232a0001c0001t0002g0229others(94): Show | 98 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.259+5067T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919173 | ||||||
| chr3:93919320
|
A | G | 1 | a0001c0010t0001g0293 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259+4920T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919320 | ||||||
| chr3:93919419
|
A | AT | 163 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.259+4820dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919419 | ||||||
| chr3:93919549
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+4691C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919549 | ||||||
| chr3:93919777
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.259+4463T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919777 | ||||||
| chr3:93919907
|
A | G | 14 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0149others(11): Show | 14 | HG00642.hp2 HG01175.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+4333T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93919907 | ||||||
| chr3:93920053
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.259+4187A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93920053 | ||||||
| chr3:93920141
|
T | C | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+4099A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93920141 | ||||||
| chr3:93920418
|
T | C | 11 | a0001c0002t0001g0214a0001c0002t0001g0228a0001c0002t0001g0231others(8): Show | 11 | HG00408.hp2 HG02080.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+3822A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93920418 | ||||||
| chr3:93920476
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.259+3764G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93920476 | ||||||
| chr3:93920587
|
A | G | 1 | a0005c0012t0001g0292 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.259+3653T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93920587 | ||||||
| chr3:93920625
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259+3615A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93920625 | ||||||
| chr3:93921129
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.259+3111C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93921129 | ||||||
| chr3:93921185
|
A | G | 1 | a0001c0002t0001g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.259+3055T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93921185 | ||||||
| chr3:93921338
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.259+2902G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93921338 | ||||||
| chr3:93921567
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259+2673C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93921567 | ||||||
| chr3:93921927
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(242): Show | 247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.259+2313A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93921927 | ||||||
| chr3:93922163
|
A | C | 1 | a0001c0002t0001g0235 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.259+2077T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93922163 | ||||||
| chr3:93922167
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259+2073A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93922167 | ||||||
| chr3:93922326
|
A | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259+1914T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93922326 | ||||||
| chr3:93922485
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+1755G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93922485 | ||||||
| chr3:93922689
|
T | C | 7 | a0001c0001t0001g0200a0001c0001t0004g0004a0001c0001t0004g0005others(4): Show | 7 | HG02280.hp2 HG02896.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+1551A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93922689 | ||||||
| chr3:93922820
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02132.hp2 NA18952.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+1420A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93922820 | ||||||
| chr3:93923019
|
C | T | 1 | a0001c0002t0001g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.259+1221G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923019 | ||||||
| chr3:93923137
|
G | T | 1 | a0001c0001t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.259+1103C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923137 | ||||||
| chr3:93923191
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259+1049G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923191 | ||||||
| chr3:93923200
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259+1040G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923200 | ||||||
| chr3:93923237
|
A | AATATTTT others(17): Show |
1 | a0001c0002t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.259+979_259+1002du others(25): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923237 | ||||||
| chr3:93923341
|
A | G | 1 | a0001c0002t0001g0226 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.259+899T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923341 | ||||||
| chr3:93923602
|
T | G | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259+638A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923602 | ||||||
| chr3:93923639
|
G | T | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259+601C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923639 | ||||||
| chr3:93923703
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.259+537A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923703 | ||||||
| chr3:93923794
|
G | A | 2 | a0001c0007t0002g0311a0001c0013t0002g0310 | 2 | NA18956.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.259+446C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923794 | ||||||
| chr3:93923894
|
G | A | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259+346C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923894 | ||||||
| chr3:93923903
|
C | CA | 36 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0055others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.259+336dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923903 | ||||||
| chr3:93923962
|
C | T | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259+278G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923962 | ||||||
| chr3:93923963
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.259+277G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923963 | ||||||
| chr3:93923967
|
A | G | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG01891.hp2 HG01952.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+273T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 3/14 | chr3 | 93923967 | ||||||
| chr3:93924655
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-391G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93924655 | ||||||
| chr3:93924663
|
C | CT | 13 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0107others(10): Show | 13 | HG01515.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-400dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93924663 | ||||||
| chr3:93924663
|
CT | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0135a0001c0001t0001g0163others(6): Show | 9 | HG00639.hp1 HG01099.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.235-400delA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93924663 | ||||||
| chr3:93924772
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.235-508G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93924772 | ||||||
| chr3:93924907
|
G | A | 1 | a0001c0002t0001g0002 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.235-643C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93924907 | ||||||
| chr3:93925283
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.235-1019T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925283 | ||||||
| chr3:93925323
|
C | G | 1 | a0006c0008t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.235-1059G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925323 | ||||||
| chr3:93925415
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.235-1151T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925415 | ||||||
| chr3:93925452
|
G | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-1188C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925452 | ||||||
| chr3:93925712
|
G | A | 92 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0223others(89): Show | 93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.235-1448C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925712 | ||||||
| chr3:93925775
|
A | G | 1 | a0001c0002t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.234+1475T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925775 | ||||||
| chr3:93925821
|
T | TA | 85 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0022others(82): Show | 86 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.234+1428dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925821 | ||||||
| chr3:93925821
|
T | TAA | 26 | a0001c0002t0001g0007a0001c0002t0001g0076a0001c0002t0001g0077others(23): Show | 26 | HG00642.hp1 HG01192.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.234+1427_234+1428d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93925821 | ||||||
| chr3:93926114
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.234+1136C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926114 | ||||||
| chr3:93926203
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(243): Show | 248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.234+1047A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926203 | ||||||
| chr3:93926354
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0186others(1): Show | 4 | NA18941.hp2 NA18945.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+896C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926354 | ||||||
| chr3:93926412
|
G | A | 1 | a0001c0001t0002g0143 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.234+838C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926412 | ||||||
| chr3:93926504
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.234+746G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926504 | ||||||
| chr3:93926539
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.234+711A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926539 | ||||||
| chr3:93926688
|
A | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0121a0001c0001t0002g0158 | 3 | NA18612.hp1 NA18963.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.234+562T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926688 | ||||||
| chr3:93926697
|
A | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0291 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.234+553T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926697 | ||||||
| chr3:93926716
|
C | T | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG01975.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+534G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926716 | ||||||
| chr3:93926723
|
A | T | 1 | a0001c0002t0001g0097 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.234+527T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926723 | ||||||
| chr3:93926943
|
CT | C | 4 | a0001c0002t0001g0146a0001c0002t0001g0178a0001c0002t0001g0179others(1): Show | 4 | NA18948.hp1 NA18973.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+306delA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93926943 | ||||||
| chr3:93927012
|
T | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18988.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.234+238A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93927012 | ||||||
| chr3:93927042
|
A | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.234+208T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93927042 | ||||||
| chr3:93927081
|
C | T | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.234+169G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93927081 | ||||||
| chr3:93927123
|
A | T | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 31 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+127T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93927123 | ||||||
| chr3:93927137
|
A | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0123 | 2 | HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.234+113T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 2/14 | chr3 | 93927137 | ||||||
| chr3:93927552
|
C | T | 92 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0223others(89): Show | 93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.77-145G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927552 | ||||||
| chr3:93927850
|
C | CAT | 13 | a0001c0001t0001g0019a0001c0001t0001g0080a0001c0001t0001g0105others(10): Show | 13 | HG01175.hp2 HG01258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.77-445_77-444dupAT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927850 | ||||||
| chr3:93927850
|
C | CATAT | 61 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0187others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.77-447_77-444dupAT others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927850 | ||||||
| chr3:93927850
|
C | CATATAT | 19 | a0001c0001t0002g0113a0001c0001t0002g0240a0001c0002t0001g0097others(16): Show | 19 | HG01168.hp1 HG01192.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.77-449_77-444dupAT others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927850 | ||||||
| chr3:93927850
|
C | CATATATA others(1): Show |
7 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0169others(4): Show | 7 | HG00741.hp1 HG01069.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.77-451_77-444dupAT others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927850 | ||||||
| chr3:93927850
|
C | CATATATA others(3): Show |
5 | a0001c0001t0001g0147a0001c0002t0001g0002a0001c0002t0001g0130others(2): Show | 6 | HG00621.hp2 HG02109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-453_77-444dupAT others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927850 | ||||||
| chr3:93927850
|
CAT | C | 117 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 117 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.77-445_77-444delAT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927850 | ||||||
| chr3:93927873
|
A | ATATG | 10 | a0001c0002t0001g0214a0001c0002t0001g0228a0001c0002t0001g0231others(7): Show | 10 | HG00408.hp2 HG02080.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.77-467_77-466insCA others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927873 | ||||||
| chr3:93927873
|
A | G | 37 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.77-466T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927873 | ||||||
| chr3:93927875
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0002g0134 | 2 | HG00558.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.77-468C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927875 | ||||||
| chr3:93927881
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.77-474T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927881 | ||||||
| chr3:93927883
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.77-476C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927883 | ||||||
| chr3:93927885
|
G | GTA | 7 | a0001c0001t0002g0003a0001c0001t0002g0087a0001c0001t0002g0191others(4): Show | 8 | HG02027.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-480_77-479dupTA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927885 | ||||||
| chr3:93927885
|
GTA | G | 32 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(29): Show | 32 | HG00621.hp1 HG01123.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.77-480_77-479delTA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927885 | ||||||
| chr3:93927887
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.77-480T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927887 | ||||||
| chr3:93927899
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-492T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927899 | ||||||
| chr3:93927911
|
G | GTGTATAT others(45): Show |
1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.77-505_77-504insTA others(50): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927911 | ||||||
| chr3:93927923
|
A | ATGTGTAT others(23): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0279 | 2 | HG02280.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.77-546_77-517dupAG others(28): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927923 | ||||||
| chr3:93927927
|
G | GTA | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(2): Show | 5 | HG00140.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-522_77-521dupTA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927927 | ||||||
| chr3:93927967
|
A | G | 2 | a0001c0001t0001g0147a0001c0002t0001g0002 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77-560T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927967 | ||||||
| chr3:93927971
|
GTGTATAT others(3): Show |
G | 2 | a0001c0001t0001g0147a0001c0002t0001g0002 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77-574_77-565delTA others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927971 | ||||||
| chr3:93927989
|
G | A | 2 | a0001c0001t0001g0147a0001c0002t0001g0002 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77-582C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927989 | ||||||
| chr3:93927991
|
G | A | 2 | a0001c0001t0001g0147a0001c0002t0001g0002 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77-584C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927991 | ||||||
| chr3:93927993
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0147a0001c0002t0001g0002 | 4 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-586C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927993 | ||||||
| chr3:93927993
|
G | GTATA | 10 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0029others(7): Show | 10 | HG00741.hp2 HG01192.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-590_77-587dupTA others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927993 | ||||||
| chr3:93927993
|
G | GTATATA | 12 | a0001c0001t0001g0025a0001c0001t0001g0066a0001c0001t0001g0067others(9): Show | 12 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.77-592_77-587dupTA others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927993 | ||||||
| chr3:93927993
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-596_77-587dupTA others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927993 | ||||||
| chr3:93927993
|
G | GTGTATAT others(3): Show |
25 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(22): Show | 25 | HG00621.hp1 HG01123.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.77-587_77-586insTA others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927993 | ||||||
| chr3:93927993
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.77-587_77-586insTA others(14): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927993 | ||||||
| chr3:93927995
|
A | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0105a0001c0001t0001g0282others(5): Show | 8 | HG00558.hp1 HG01928.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-588T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93927995 | ||||||
| chr3:93928001
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77-594T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928001 | ||||||
| chr3:93928010
|
TA | T | 2 | a0001c0001t0001g0147a0001c0002t0001g0002 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77-604delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928010 | ||||||
| chr3:93928011
|
A | ATATAT | 16 | a0001c0001t0001g0009a0001c0001t0001g0125a0001c0001t0001g0126others(13): Show | 16 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.77-605_77-604insAT others(3): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928011 | ||||||
| chr3:93928011
|
A | ATATATAT | 45 | a0001c0001t0001g0032a0001c0001t0001g0187a0001c0001t0001g0223others(42): Show | 45 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.77-605_77-604insAT others(5): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928011 | ||||||
| chr3:93928011
|
A | ATATATAT others(2): Show |
14 | a0001c0002t0001g0099a0001c0002t0001g0103a0001c0002t0001g0137others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.77-605_77-604insAT others(7): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928011 | ||||||
| chr3:93928011
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0230 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77-605_77-604insAT others(9): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928011 | ||||||
| chr3:93928011
|
A | ATATATT | 26 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(23): Show | 26 | HG00642.hp2 HG01069.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.77-605_77-604insAA others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928011 | ||||||
| chr3:93928012
|
T | TA | 36 | a0001c0001t0001g0105a0001c0001t0001g0144a0001c0001t0002g0071others(33): Show | 36 | HG01074.hp1 HG01106.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.77-606_77-605insT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928012 | ||||||
| chr3:93928012
|
T | TATA | 5 | a0001c0001t0002g0003a0001c0001t0002g0191a0001c0001t0002g0220others(2): Show | 6 | HG02486.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-606_77-605insTA others(1): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928012 | ||||||
| chr3:93928012
|
T | TATATA | 45 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(42): Show | 46 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.77-606_77-605insTA others(3): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928012 | ||||||
| chr3:93928012
|
T | TATATATA | 20 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0023others(17): Show | 20 | HG01256.hp2 HG01358.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.77-606_77-605insTA others(5): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928012 | ||||||
| chr3:93928012
|
T | TATATATA others(2): Show |
13 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0282others(10): Show | 13 | HG00558.hp1 HG02280.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.77-606_77-605insTA others(7): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928012 | ||||||
| chr3:93928013
|
T | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00609.hp2 HG00621.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.77-606A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928013 | ||||||
| chr3:93928014
|
T | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0282others(2): Show | 5 | HG00558.hp1 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-607A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928014 | ||||||
| chr3:93928015
|
T | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0279a0001c0001t0001g0295 | 3 | NA18978.hp1 NA18982.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.77-608A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928015 | ||||||
| chr3:93928037
|
C | A | 2 | a0001c0001t0002g0240a0001c0002t0001g0247 | 2 | NA18993.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.77-630G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928037 | ||||||
| chr3:93928038
|
G | A | 2 | a0001c0001t0002g0240a0001c0002t0001g0247 | 2 | NA18993.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.77-631C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928038 | ||||||
| chr3:93928321
|
T | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.77-914A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928321 | ||||||
| chr3:93928435
|
GA | G | 5 | a0001c0001t0002g0124a0001c0001t0002g0133a0001c0001t0002g0151others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-1029delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928435 | ||||||
| chr3:93928447
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.77-1040A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928447 | ||||||
| chr3:93928533
|
C | CA | 18 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0049others(15): Show | 18 | HG01099.hp2 HG01175.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.77-1127dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93928533 | ||||||
| chr3:93929051
|
T | C | 3 | a0001c0002t0001g0243a0001c0002t0001g0244a0001c0002t0001g0248 | 3 | HG01192.hp2 HG01358.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.77-1644A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93929051 | ||||||
| chr3:93929428
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.77-2021G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93929428 | ||||||
| chr3:93930176
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.77-2769G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93930176 | ||||||
| chr3:93930207
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.77-2800C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93930207 | ||||||
| chr3:93930432
|
T | C | 2 | a0001c0001t0001g0200a0001c0009t0001g0139 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.77-3025A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93930432 | ||||||
| chr3:93930742
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.77-3335G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93930742 | ||||||
| chr3:93931038
|
T | C | 14 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0149others(11): Show | 14 | HG00642.hp2 HG01175.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.77-3631A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931038 | ||||||
| chr3:93931095
|
C | T | 96 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0223others(93): Show | 97 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.77-3688G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931095 | ||||||
| chr3:93931096
|
G | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-3689C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931096 | ||||||
| chr3:93931135
|
A | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG01891.hp2 HG01952.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-3728T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931135 | ||||||
| chr3:93931218
|
C | T | 2 | a0001c0001t0001g0084a0004c0014t0001g0088 | 2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.77-3811G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931218 | ||||||
| chr3:93931237
|
C | A | 1 | a0001c0002t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.77-3830G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931237 | ||||||
| chr3:93931315
|
T | A | 1 | a0001c0002t0001g0154 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.77-3908A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931315 | ||||||
| chr3:93931547
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.77-4140A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931547 | ||||||
| chr3:93931664
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.77-4257C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931664 | ||||||
| chr3:93931694
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-4287A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931694 | ||||||
| chr3:93931705
|
TTCTGGAA others(24): Show |
T | 2 | a0001c0002t0001g0207a0001c0002t0001g0245 | 2 | NA18952.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.77-4329_77-4299del others(31): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931705 | ||||||
| chr3:93931734
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0039 | 3 | HG01496.hp1 HG01952.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.77-4327G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931734 | ||||||
| chr3:93931760
|
A | G | 21 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0148others(18): Show | 21 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.77-4353T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931760 | ||||||
| chr3:93931901
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.77-4494G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931901 | ||||||
| chr3:93931935
|
G | GTCCTTTA others(3): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0020others(7): Show | 10 | HG02083.hp1 HG02132.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-4538_77-4529dup others(10): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931935 | ||||||
| chr3:93931940
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77-4533A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93931940 | ||||||
| chr3:93932094
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.77-4687C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93932094 | ||||||
| chr3:93932269
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.77-4862A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93932269 | ||||||
| chr3:93932559
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.77-5152A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93932559 | ||||||
| chr3:93932572
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-5165G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93932572 | ||||||
| chr3:93933649
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77-6242G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933649 | ||||||
| chr3:93933650
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.77-6243C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933650 | ||||||
| chr3:93933686
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.77-6279C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933686 | ||||||
| chr3:93933690
|
G | A | 1 | a0001c0002t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.77-6283C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933690 | ||||||
| chr3:93933755
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.77-6348G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933755 | ||||||
| chr3:93933758
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-6351A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933758 | ||||||
| chr3:93933838
|
G | T | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.77-6431C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933838 | ||||||
| chr3:93933872
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.77-6465C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933872 | ||||||
| chr3:93933941
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0064a0001c0002t0001g0213 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-6534C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933941 | ||||||
| chr3:93933964
|
G | A | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.77-6557C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933964 | ||||||
| chr3:93933988
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0048 | 2 | NA18954.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.77-6581C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93933988 | ||||||
| chr3:93934008
|
C | CA | 26 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0148others(23): Show | 27 | HG00642.hp2 HG01106.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.77-6602dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934008 | ||||||
| chr3:93934008
|
C | CAA | 7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG00408.hp1 HG00438.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.77-6603_77-6602dup others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934008 | ||||||
| chr3:93934008
|
CA | C | 97 | a0001c0001t0001g0044a0001c0001t0001g0063a0001c0001t0001g0147others(94): Show | 98 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.77-6602delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934008 | ||||||
| chr3:93934008
|
CAA | C | 6 | a0001c0002t0001g0097a0001c0002t0001g0215a0001c0002t0001g0227others(3): Show | 6 | HG01993.hp2 HG02027.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-6603_77-6602del others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934008 | ||||||
| chr3:93934142
|
T | G | 2 | a0001c0001t0001g0147a0001c0002t0001g0002 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77-6735A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934142 | ||||||
| chr3:93934253
|
AAAATGTA others(3): Show |
A | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.77-6856_77-6847del others(10): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934253 | ||||||
| chr3:93934268
|
T | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.77-6861A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934268 | ||||||
| chr3:93934372
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.77-6965G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934372 | ||||||
| chr3:93934375
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.77-6968C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934375 | ||||||
| chr3:93934488
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.77-7081G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934488 | ||||||
| chr3:93934539
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.77-7132C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934539 | ||||||
| chr3:93934577
|
A | G | 3 | a0002c0004t0001g0183a0002c0004t0001g0184a0002c0004t0001g0219 | 3 | HG02280.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.77-7170T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934577 | ||||||
| chr3:93934663
|
AAAG | A | 3 | a0001c0001t0002g0073a0001c0001t0004g0004a0001c0001t0004g0005 | 3 | HG02896.hp1 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77-7259_77-7257del others(3): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934663 | ||||||
| chr3:93934707
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-7300C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934707 | ||||||
| chr3:93934717
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.77-7310T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934717 | ||||||
| chr3:93934726
|
A | T | 4 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0118others(1): Show | 4 | HG02083.hp2 HG02165.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-7319T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93934726 | ||||||
| chr3:93935129
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.77-7722C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93935129 | ||||||
| chr3:93935148
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 61 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.77-7741C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93935148 | ||||||
| chr3:93935245
|
C | A | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG01891.hp2 HG01952.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-7838G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93935245 | ||||||
| chr3:93935380
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.77-7973A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93935380 | ||||||
| chr3:93935676
|
T | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0306a0001c0001t0007g0305others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-8269A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93935676 | ||||||
| chr3:93935955
|
TA | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0034others(5): Show | 8 | HG01261.hp2 HG01943.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-8549delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93935955 | ||||||
| chr3:93936215
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.77-8808T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93936215 | ||||||
| chr3:93936239
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.77-8832T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93936239 | ||||||
| chr3:93936504
|
A | G | 5 | a0001c0001t0001g0147a0001c0002t0001g0002a0001c0002t0001g0054others(2): Show | 6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-9097T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93936504 | ||||||
| chr3:93936892
|
A | G | 2 | a0001c0001t0001g0302a0001c0001t0001g0304 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.77-9485T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93936892 | ||||||
| chr3:93936953
|
G | T | 1 | a0001c0001t0002g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.77-9546C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93936953 | ||||||
| chr3:93937047
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.77-9640G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937047 | ||||||
| chr3:93937147
|
C | T | 1 | a0001c0002t0001g0208 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.77-9740G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937147 | ||||||
| chr3:93937219
|
G | A | 37 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(34): Show | 37 | HG00558.hp1 HG00621.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.77-9812C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937219 | ||||||
| chr3:93937247
|
G | A | 2 | a0001c0001t0001g0298a0003c0003t0001g0210 | 2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.77-9840C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937247 | ||||||
| chr3:93937327
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77-9920G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937327 | ||||||
| chr3:93937368
|
AT | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 237 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.77-9962delA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937368 | ||||||
| chr3:93937406
|
C | T | 6 | a0001c0001t0001g0144a0001c0001t0002g0143a0001c0001t0002g0201others(3): Show | 6 | HG00558.hp2 NA18954.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-9999G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937406 | ||||||
| chr3:93937466
|
C | T | 1 | a0001c0009t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77-10059G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937466 | ||||||
| chr3:93937517
|
G | A | 1 | a0001c0001t0008g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.77-10110C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937517 | ||||||
| chr3:93937610
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.77-10203C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937610 | ||||||
| chr3:93937728
|
C | T | 14 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0149others(11): Show | 14 | HG00642.hp2 HG01175.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.77-10321G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937728 | ||||||
| chr3:93937761
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.77-10354C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937761 | ||||||
| chr3:93937785
|
A | C | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.77-10378T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937785 | ||||||
| chr3:93937847
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.77-10440T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937847 | ||||||
| chr3:93937910
|
C | T | 1 | a0001c0002t0001g0290 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77-10503G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93937910 | ||||||
| chr3:93938235
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.77-10828G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938235 | ||||||
| chr3:93938248
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.77-10841C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938248 | ||||||
| chr3:93938306
|
C | T | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77-10899G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938306 | ||||||
| chr3:93938330
|
T | C | 1 | a0001c0002t0001g0218 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.77-10923A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938330 | ||||||
| chr3:93938462
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0035others(1): Show | 4 | HG00733.hp1 HG00741.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-11055C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938462 | ||||||
| chr3:93938487
|
T | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.77-11080A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938487 | ||||||
| chr3:93938501
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0002g0087 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.77-11094C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938501 | ||||||
| chr3:93938511
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-11104G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938511 | ||||||
| chr3:93938512
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 61 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.77-11105C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938512 | ||||||
| chr3:93938528
|
A | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0307a0001c0001t0004g0004others(2): Show | 5 | HG02896.hp2 HG03195.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-11121T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938528 | ||||||
| chr3:93938633
|
A | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.77-11226T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938633 | ||||||
| chr3:93938681
|
GT | G | 5 | a0001c0001t0001g0144a0001c0001t0002g0143a0001c0001t0002g0201others(2): Show | 5 | NA18954.hp1 NA18956.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-11275delA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938681 | ||||||
| chr3:93938767
|
C | T | 6 | a0001c0001t0002g0229a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-11360G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938767 | ||||||
| chr3:93938770
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77-11363G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938770 | ||||||
| chr3:93938914
|
G | T | 1 | a0001c0002t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.77-11507C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93938914 | ||||||
| chr3:93939003
|
C | T | 1 | a0004c0014t0001g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.77-11596G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939003 | ||||||
| chr3:93939006
|
T | C | 5 | a0001c0001t0001g0147a0001c0002t0001g0002a0001c0002t0001g0054others(2): Show | 6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-11599A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939006 | ||||||
| chr3:93939084
|
C | T | 1 | a0001c0013t0002g0310 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.77-11677G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939084 | ||||||
| chr3:93939266
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.77-11859A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939266 | ||||||
| chr3:93939342
|
T | C | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77-11935A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939342 | ||||||
| chr3:93939483
|
C | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG01891.hp2 HG01952.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-12076G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939483 | ||||||
| chr3:93939584
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.77-12177G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939584 | ||||||
| chr3:93939728
|
T | C | 4 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0130others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-12321A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939728 | ||||||
| chr3:93939736
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.77-12329G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939736 | ||||||
| chr3:93939808
|
T | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | NA18973.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.77-12401A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939808 | ||||||
| chr3:93939825
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.77-12418C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939825 | ||||||
| chr3:93939857
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0002g0229a0001c0002t0001g0236 | 3 | HG04199.hp1 NA18940.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.77-12450C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939857 | ||||||
| chr3:93939926
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.77-12519C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93939926 | ||||||
| chr3:93940019
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.77-12612C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940019 | ||||||
| chr3:93940233
|
C | T | 1 | a0001c0001t0007g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77-12826G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940233 | ||||||
| chr3:93940362
|
A | T | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.77-12955T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940362 | ||||||
| chr3:93940409
|
A | C | 3 | a0001c0001t0002g0113a0001c0001t0002g0121a0001c0001t0002g0158 | 3 | NA18612.hp1 NA18963.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.77-13002T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940409 | ||||||
| chr3:93940720
|
C | G | 1 | a0009c0005t0002g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.77-13313G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940720 | ||||||
| chr3:93940902
|
C | T | 10 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0206others(7): Show | 10 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.77-13495G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940902 | ||||||
| chr3:93940944
|
C | T | 101 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0223others(98): Show | 102 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.77-13537G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940944 | ||||||
| chr3:93940975
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.77-13568G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93940975 | ||||||
| chr3:93941001
|
C | A | 5 | a0001c0001t0001g0147a0001c0002t0001g0002a0001c0002t0001g0054others(2): Show | 6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-13594G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941001 | ||||||
| chr3:93941111
|
C | T | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77-13704G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941111 | ||||||
| chr3:93941128
|
C | T | 1 | a0001c0002t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.77-13721G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941128 | ||||||
| chr3:93941449
|
G | A | 1 | a0001c0002t0001g0098 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.77-14042C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941449 | ||||||
| chr3:93941562
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.77-14155G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941562 | ||||||
| chr3:93941800
|
A | G | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77-14393T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941800 | ||||||
| chr3:93941881
|
C | A | 1 | a0001c0002t0001g0290 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77-14474G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941881 | ||||||
| chr3:93941889
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG01123.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-14482C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941889 | ||||||
| chr3:93941941
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.77-14534A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93941941 | ||||||
| chr3:93942104
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.77-14697A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942104 | ||||||
| chr3:93942186
|
T | C | 1 | a0001c0001t0007g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77-14779A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942186 | ||||||
| chr3:93942229
|
C | T | 102 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0223others(99): Show | 103 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.77-14822G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942229 | ||||||
| chr3:93942230
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(5): Show | 8 | NA18954.hp2 NA18959.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-14823C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942230 | ||||||
| chr3:93942633
|
G | A | 1 | a0001c0001t0009g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77-15226C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942633 | ||||||
| chr3:93942656
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.77-15249T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942656 | ||||||
| chr3:93942970
|
C | A | 1 | a0001c0001t0002g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.77-15563G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93942970 | ||||||
| chr3:93943018
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.77-15611C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943018 | ||||||
| chr3:93943093
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.77-15686C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943093 | ||||||
| chr3:93943106
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.77-15699G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943106 | ||||||
| chr3:93943331
|
G | A | 5 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0130others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-15924C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943331 | ||||||
| chr3:93943429
|
T | TCCAGGCC others(751): Show |
3 | a0002c0004t0001g0183a0002c0004t0001g0184a0002c0004t0001g0219 | 3 | HG02280.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.77-16780_77-16023d others(760): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943429 | ||||||
| chr3:93943778
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77-16371T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943778 | ||||||
| chr3:93943886
|
G | C | 1 | a0001c0002t0001g0266 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.77-16479C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93943886 | ||||||
| chr3:93944060
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.77-16653T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944060 | ||||||
| chr3:93944168
|
GAAGA | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.77-16765_77-16762d others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944168 | ||||||
| chr3:93944275
|
G | A | 6 | a0001c0001t0002g0229a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-16868C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944275 | ||||||
| chr3:93944456
|
T | C | 1 | a0001c0001t0003g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.77-17049A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944456 | ||||||
| chr3:93944468
|
A | G | 8 | a0001c0001t0001g0044a0001c0001t0001g0065a0001c0001t0001g0125others(5): Show | 8 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-17061T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944468 | ||||||
| chr3:93944606
|
A | G | 1 | a0008c0011t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.77-17199T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944606 | ||||||
| chr3:93944644
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0136 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.77-17237T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944644 | ||||||
| chr3:93944659
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77-17252A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944659 | ||||||
| chr3:93944732
|
T | C | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77-17325A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944732 | ||||||
| chr3:93944768
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.77-17361G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944768 | ||||||
| chr3:93944796
|
T | A | 1 | a0001c0001t0001g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.77-17389A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944796 | ||||||
| chr3:93944845
|
T | C | 1 | a0001c0002t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77-17438A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944845 | ||||||
| chr3:93944905
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.77-17498A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944905 | ||||||
| chr3:93944960
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.77-17553G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93944960 | ||||||
| chr3:93945060
|
A | T | 1 | a0001c0002t0001g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.77-17653T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945060 | ||||||
| chr3:93945208
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.77-17801C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945208 | ||||||
| chr3:93945277
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.77-17870T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945277 | ||||||
| chr3:93945335
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-17928G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945335 | ||||||
| chr3:93945336
|
T | G | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-17929A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945336 | ||||||
| chr3:93945350
|
C | A | 3 | a0001c0001t0001g0084a0001c0001t0008g0155a0004c0014t0001g0088 | 3 | HG00639.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.77-17943G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945350 | ||||||
| chr3:93945355
|
A | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-17948T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945355 | ||||||
| chr3:93945369
|
G | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-17962C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945369 | ||||||
| chr3:93945383
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-17976G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945383 | ||||||
| chr3:93945401
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-17994C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945401 | ||||||
| chr3:93945442
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18035G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945442 | ||||||
| chr3:93945459
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-18052G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945459 | ||||||
| chr3:93945474
|
G | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18067C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945474 | ||||||
| chr3:93945478
|
A | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18071T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945478 | ||||||
| chr3:93945486
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18079T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945486 | ||||||
| chr3:93945489
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18082C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945489 | ||||||
| chr3:93945490
|
G | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18083C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945490 | ||||||
| chr3:93945500
|
T | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18093A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945500 | ||||||
| chr3:93945504
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18097G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945504 | ||||||
| chr3:93945510
|
T | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18103A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945510 | ||||||
| chr3:93945523
|
C | G | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18116G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945523 | ||||||
| chr3:93945531
|
T | G | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18124A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945531 | ||||||
| chr3:93945537
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18130C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945537 | ||||||
| chr3:93945546
|
T | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18139A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945546 | ||||||
| chr3:93945570
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18163G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945570 | ||||||
| chr3:93945594
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18187G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945594 | ||||||
| chr3:93945595
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18188T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945595 | ||||||
| chr3:93945596
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18189C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945596 | ||||||
| chr3:93945611
|
T | C | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18204A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945611 | ||||||
| chr3:93945636
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18229C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945636 | ||||||
| chr3:93945637
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18230G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945637 | ||||||
| chr3:93945654
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18247C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945654 | ||||||
| chr3:93945660
|
C | G | 1 | a0001c0002t0001g0214 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.77-18253G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945660 | ||||||
| chr3:93945687
|
AC | A | 3 | a0001c0001t0001g0084a0001c0001t0008g0155a0004c0014t0001g0088 | 3 | HG00639.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.77-18281delG | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945687 | ||||||
| chr3:93945692
|
C | A | 3 | a0001c0001t0001g0084a0001c0001t0008g0155a0004c0014t0001g0088 | 3 | HG00639.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.77-18285G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945692 | ||||||
| chr3:93945810
|
G | C | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG01975.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-18403C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93945810 | ||||||
| chr3:93946044
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | NA18943.hp2 NA18978.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-18637G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946044 | ||||||
| chr3:93946045
|
G | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | NA18943.hp2 NA18978.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-18638C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946045 | ||||||
| chr3:93946111
|
C | A | 1 | a0001c0001t0001g0279 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.77-18704G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946111 | ||||||
| chr3:93946212
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.77-18805G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946212 | ||||||
| chr3:93946484
|
A | C | 1 | a0001c0001t0002g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.77-19077T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946484 | ||||||
| chr3:93946558
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.77-19151C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946558 | ||||||
| chr3:93946604
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.77-19197A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946604 | ||||||
| chr3:93946723
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-19316A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946723 | ||||||
| chr3:93946805
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77-19398A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946805 | ||||||
| chr3:93946838
|
G | GA | 31 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0059others(28): Show | 31 | HG00438.hp2 HG00639.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.77-19432dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946838 | ||||||
| chr3:93946838
|
G | GAA | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG01496.hp1 HG01952.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-19433_77-19432d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946838 | ||||||
| chr3:93946838
|
GA | G | 6 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0306others(3): Show | 6 | HG00642.hp2 HG03486.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-19432delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946838 | ||||||
| chr3:93946838
|
GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0002g0195 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.77-19443_77-19432d others(14): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946838 | ||||||
| chr3:93946997
|
A | G | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.77-19590T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93946997 | ||||||
| chr3:93947041
|
T | G | 1 | a0001c0001t0007g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77-19634A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947041 | ||||||
| chr3:93947107
|
A | C | 1 | a0001c0002t0001g0266 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.77-19700T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947107 | ||||||
| chr3:93947294
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.77-19887G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947294 | ||||||
| chr3:93947329
|
T | C | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77-19922A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947329 | ||||||
| chr3:93947338
|
A | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-19931T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947338 | ||||||
| chr3:93947658
|
C | T | 2 | a0001c0001t0001g0200a0001c0009t0001g0139 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.77-20251G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947658 | ||||||
| chr3:93947746
|
T | G | 7 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-20339A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947746 | ||||||
| chr3:93947789
|
A | C | 1 | a0001c0002t0001g0226 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.77-20382T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947789 | ||||||
| chr3:93947929
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.77-20522T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947929 | ||||||
| chr3:93947954
|
A | T | 5 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-20547T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947954 | ||||||
| chr3:93947971
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0136 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.77-20564G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93947971 | ||||||
| chr3:93948072
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.77-20665G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948072 | ||||||
| chr3:93948128
|
G | C | 1 | a0001c0002t0001g0266 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.77-20721C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948128 | ||||||
| chr3:93948137
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-20730T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948137 | ||||||
| chr3:93948345
|
T | A | 1 | a0001c0001t0001g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.77-20938A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948345 | ||||||
| chr3:93948403
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.77-20996A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948403 | ||||||
| chr3:93948480
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.77-21073C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948480 | ||||||
| chr3:93948926
|
A | G | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.77-21519T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948926 | ||||||
| chr3:93948960
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.77-21553A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93948960 | ||||||
| chr3:93949008
|
A | T | 1 | a0001c0002t0001g0231 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.77-21601T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949008 | ||||||
| chr3:93949029
|
T | C | 13 | a0001c0001t0001g0147a0001c0002t0001g0002a0001c0002t0001g0054others(10): Show | 14 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.77-21622A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949029 | ||||||
| chr3:93949156
|
G | A | 1 | a0009c0005t0002g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.77-21749C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949156 | ||||||
| chr3:93949343
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.77-21936C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949343 | ||||||
| chr3:93949465
|
C | T | 1 | a0001c0002t0001g0290 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77-22058G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949465 | ||||||
| chr3:93949626
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-22219T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949626 | ||||||
| chr3:93949950
|
G | T | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77-22543C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93949950 | ||||||
| chr3:93950050
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.77-22643C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950050 | ||||||
| chr3:93950276
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.77-22869T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950276 | ||||||
| chr3:93950507
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.77-23100G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950507 | ||||||
| chr3:93950572
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+23102C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950572 | ||||||
| chr3:93950703
|
A | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0075 | 2 | HG01074.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.76+22971T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950703 | ||||||
| chr3:93950727
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.76+22947G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950727 | ||||||
| chr3:93950848
|
T | C | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.76+22826A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950848 | ||||||
| chr3:93950866
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76+22808G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93950866 | ||||||
| chr3:93951264
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.76+22410C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951264 | ||||||
| chr3:93951302
|
C | A | 1 | a0001c0001t0002g0158 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.76+22372G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951302 | ||||||
| chr3:93951349
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76+22325G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951349 | ||||||
| chr3:93951350
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | NA18943.hp2 NA18986.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+22324C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951350 | ||||||
| chr3:93951386
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.76+22288A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951386 | ||||||
| chr3:93951399
|
G | A | 15 | a0001c0002t0001g0006a0001c0002t0001g0099a0001c0002t0001g0103others(12): Show | 15 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.76+22275C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951399 | ||||||
| chr3:93951683
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.76+21991A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951683 | ||||||
| chr3:93951786
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.76+21888G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93951786 | ||||||
| chr3:93952011
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.76+21663G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952011 | ||||||
| chr3:93952068
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.76+21606G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952068 | ||||||
| chr3:93952228
|
C | A | 1 | a0001c0002t0001g0174 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.76+21446G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952228 | ||||||
| chr3:93952229
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.76+21445A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952229 | ||||||
| chr3:93952269
|
A | T | 1 | a0001c0001t0002g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.76+21405T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952269 | ||||||
| chr3:93952339
|
C | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 58 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.76+21335G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952339 | ||||||
| chr3:93952341
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.76+21333G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952341 | ||||||
| chr3:93952472
|
A | G | 9 | a0001c0001t0001g0142a0001c0001t0001g0152a0001c0001t0001g0153others(6): Show | 9 | HG00642.hp2 HG01175.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76+21202T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952472 | ||||||
| chr3:93952492
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.76+21182T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952492 | ||||||
| chr3:93952728
|
C | A | 1 | a0001c0002t0001g0137 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.76+20946G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952728 | ||||||
| chr3:93952799
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76+20875A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952799 | ||||||
| chr3:93952815
|
A | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG01891.hp2 HG01952.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+20859T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952815 | ||||||
| chr3:93952817
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.76+20857A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952817 | ||||||
| chr3:93952888
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.76+20786T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93952888 | ||||||
| chr3:93953032
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.76+20642C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953032 | ||||||
| chr3:93953033
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.76+20641T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953033 | ||||||
| chr3:93953053
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.76+20621A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953053 | ||||||
| chr3:93953122
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.76+20552C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953122 | ||||||
| chr3:93953224
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+20450A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953224 | ||||||
| chr3:93953488
|
A | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+20186T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953488 | ||||||
| chr3:93953490
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.76+20184G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953490 | ||||||
| chr3:93953515
|
C | T | 5 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0130others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+20159G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953515 | ||||||
| chr3:93953517
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.76+20157T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953517 | ||||||
| chr3:93953554
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+20120T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953554 | ||||||
| chr3:93953571
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+20103A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953571 | ||||||
| chr3:93953603
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+20071T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953603 | ||||||
| chr3:93953653
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.76+20021A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953653 | ||||||
| chr3:93953672
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.76+20002G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953672 | ||||||
| chr3:93953672
|
CG | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 58 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.76+20001delC | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953672 | ||||||
| chr3:93953969
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.76+19705G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93953969 | ||||||
| chr3:93954038
|
G | T | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76+19636C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954038 | ||||||
| chr3:93954041
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.76+19633C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954041 | ||||||
| chr3:93954132
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0291 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.76+19542G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954132 | ||||||
| chr3:93954225
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.76+19449G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954225 | ||||||
| chr3:93954404
|
C | A | 1 | a0001c0001t0002g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.76+19270G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954404 | ||||||
| chr3:93954571
|
T | G | 3 | a0001c0002t0001g0054a0001c0002t0001g0131a0001c0002t0001g0188 | 3 | HG01884.hp2 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.76+19103A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954571 | ||||||
| chr3:93954764
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.76+18910C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954764 | ||||||
| chr3:93954916
|
G | A | 1 | a0001c0002t0001g0259 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.76+18758C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93954916 | ||||||
| chr3:93955080
|
G | T | 3 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0167 | 3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76+18594C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955080 | ||||||
| chr3:93955289
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.76+18385G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955289 | ||||||
| chr3:93955290
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76+18384C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955290 | ||||||
| chr3:93955310
|
A | G | 21 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0148others(18): Show | 21 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.76+18364T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955310 | ||||||
| chr3:93955410
|
G | A | 1 | a0001c0002t0001g0213 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.76+18264C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955410 | ||||||
| chr3:93955462
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.76+18212T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955462 | ||||||
| chr3:93955542
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0002g0229a0001c0002t0001g0236 | 3 | HG02630.hp1 NA18940.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.76+18132G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955542 | ||||||
| chr3:93955661
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.76+18013G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955661 | ||||||
| chr3:93955691
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.76+17983C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955691 | ||||||
| chr3:93955703
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76+17971A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955703 | ||||||
| chr3:93955722
|
T | TA | 10 | a0001c0001t0001g0135a0001c0001t0001g0190a0001c0001t0001g0298others(7): Show | 10 | HG00408.hp1 HG00438.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.76+17951dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955722 | ||||||
| chr3:93955722
|
T | TAA | 14 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0149others(11): Show | 14 | HG00642.hp2 HG01175.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.76+17950_76+17951d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93955722 | ||||||
| chr3:93956010
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.76+17664A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956010 | ||||||
| chr3:93956124
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.76+17550A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956124 | ||||||
| chr3:93956236
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0002g0106 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.76+17438A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956236 | ||||||
| chr3:93956371
|
C | T | 102 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0223others(99): Show | 103 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.76+17303G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956371 | ||||||
| chr3:93956533
|
T | TAC | 8 | a0001c0001t0002g0145a0001c0001t0002g0151a0001c0001t0002g0164others(5): Show | 8 | HG02055.hp1 HG02976.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+17139_76+17140d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956533 | ||||||
| chr3:93956535
|
CACACACA others(21): Show |
C | 55 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 56 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.76+17111_76+17138d others(30): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956535 | ||||||
| chr3:93956537
|
CACACACA others(19): Show |
C | 2 | a0001c0001t0001g0015a0001c0001t0001g0035 | 2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.76+17111_76+17136d others(28): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956537 | ||||||
| chr3:93956549
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.76+17125G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956549 | ||||||
| chr3:93956549
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.76+17111_76+17124d others(16): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956549 | ||||||
| chr3:93956551
|
CACACACA others(5): Show |
C | 2 | a0001c0001t0001g0136a0001c0001t0001g0200 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.76+17111_76+17122d others(14): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956551 | ||||||
| chr3:93956557
|
C | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76+17117G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956557 | ||||||
| chr3:93956557
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.76+17116_76+17117i others(12): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956557 | ||||||
| chr3:93956559
|
C | CACACACA others(5): Show |
1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.76+17114_76+17115i others(14): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956559 | ||||||
| chr3:93956561
|
C | A | 7 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00408.hp1 HG00438.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.76+17113G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956561 | ||||||
| chr3:93956561
|
C | CACAA | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0084others(17): Show | 21 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.76+17112_76+17113i others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956561 | ||||||
| chr3:93956561
|
C | CACACACA others(3): Show |
22 | a0001c0001t0001g0060a0001c0001t0001g0270a0001c0001t0001g0271others(19): Show | 22 | HG00558.hp1 HG01256.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.76+17112_76+17113i others(12): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956561 | ||||||
| chr3:93956561
|
C | CACACACA others(5): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0279 | 3 | HG02738.hp1 NA18978.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.76+17112_76+17113i others(14): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956561 | ||||||
| chr3:93956561
|
C | CACACACA others(7): Show |
1 | a0001c0001t0001g0287 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.76+17112_76+17113i others(16): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956561 | ||||||
| chr3:93956563
|
A | AAC | 63 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0095others(60): Show | 63 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.76+17109_76+17110d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956563 | ||||||
| chr3:93956563
|
A | AACAC | 72 | a0001c0001t0001g0126a0001c0001t0001g0138a0001c0001t0001g0187others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.76+17107_76+17110d others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956563 | ||||||
| chr3:93956563
|
A | AACACAC | 7 | a0001c0001t0002g0114a0001c0002t0001g0168a0001c0002t0001g0169others(4): Show | 7 | HG01069.hp1 HG01123.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.76+17105_76+17110d others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956563 | ||||||
| chr3:93956563
|
A | C | 61 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(58): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.76+17111T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956563 | ||||||
| chr3:93956563
|
AAC | A | 7 | a0001c0001t0002g0119a0001c0001t0002g0229a0001c0002t0001g0215others(4): Show | 7 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.76+17109_76+17110d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956563 | ||||||
| chr3:93956747
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.76+16927T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956747 | ||||||
| chr3:93956880
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76+16794G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956880 | ||||||
| chr3:93956895
|
C | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(293): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.76+16779G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93956895 | ||||||
| chr3:93957029
|
C | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.76+16645G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93957029 | ||||||
| chr3:93957522
|
G | A | 5 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0130others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+16152C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93957522 | ||||||
| chr3:93957719
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+15955G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93957719 | ||||||
| chr3:93957766
|
G | C | 1 | a0001c0001t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76+15908C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93957766 | ||||||
| chr3:93957798
|
A | G | 1 | a0001c0002t0001g0227 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.76+15876T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93957798 | ||||||
| chr3:93957879
|
A | G | 1 | a0001c0002t0001g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.76+15795T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93957879 | ||||||
| chr3:93958230
|
G | T | 3 | a0001c0001t0002g0113a0001c0001t0002g0121a0001c0001t0002g0158 | 3 | NA18612.hp1 NA18963.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.76+15444C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93958230 | ||||||
| chr3:93958860
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+14814G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93958860 | ||||||
| chr3:93958934
|
T | C | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.76+14740A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93958934 | ||||||
| chr3:93959023
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.76+14651A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93959023 | ||||||
| chr3:93959432
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.76+14242G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93959432 | ||||||
| chr3:93959566
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.76+14108A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93959566 | ||||||
| chr3:93959750
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.76+13924T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93959750 | ||||||
| chr3:93959849
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0306a0001c0001t0007g0305others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+13825C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93959849 | ||||||
| chr3:93960062
|
C | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0291 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.76+13612G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960062 | ||||||
| chr3:93960109
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.76+13565C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960109 | ||||||
| chr3:93960401
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.76+13273G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960401 | ||||||
| chr3:93960465
|
C | T | 1 | a0001c0002t0001g0174 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.76+13209G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960465 | ||||||
| chr3:93960532
|
C | CT | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0042others(48): Show | 52 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.76+13141dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960532 | ||||||
| chr3:93960532
|
CT | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0082others(17): Show | 20 | HG00558.hp2 HG00639.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.76+13141delA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960532 | ||||||
| chr3:93960532
|
CTT | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0095others(3): Show | 6 | HG02615.hp2 HG02738.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.76+13140_76+13141d others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960532 | ||||||
| chr3:93960680
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.76+12994T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960680 | ||||||
| chr3:93960863
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.76+12811A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960863 | ||||||
| chr3:93960987
|
G | GA | 12 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0002g0106others(9): Show | 12 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.76+12686dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93960987 | ||||||
| chr3:93961119
|
T | G | 3 | a0001c0001t0001g0144a0001c0001t0002g0143a0001c0001t0002g0201 | 3 | NA18954.hp1 NA18957.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.76+12555A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93961119 | ||||||
| chr3:93961489
|
A | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0306a0001c0001t0007g0305others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+12185T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93961489 | ||||||
| chr3:93961781
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.76+11893C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93961781 | ||||||
| chr3:93962183
|
T | A | 30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.76+11491A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93962183 | ||||||
| chr3:93962254
|
C | T | 1 | a0007c0006t0001g0262 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.76+11420G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93962254 | ||||||
| chr3:93962488
|
G | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0284others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+11186C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93962488 | ||||||
| chr3:93962506
|
A | G | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG01258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.76+11168T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93962506 | ||||||
| chr3:93962645
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 61 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.76+11029G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93962645 | ||||||
| chr3:93963049
|
T | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76+10625A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963049 | ||||||
| chr3:93963374
|
G | A | 1 | a0001c0002t0001g0277 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.76+10300C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963374 | ||||||
| chr3:93963405
|
A | T | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG01975.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+10269T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963405 | ||||||
| chr3:93963430
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0191a0001c0001t0002g0220others(1): Show | 5 | HG02486.hp2 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+10244G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963430 | ||||||
| chr3:93963532
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76+10142C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963532 | ||||||
| chr3:93963653
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.76+10021C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963653 | ||||||
| chr3:93963699
|
TAGA | T | 100 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0223others(97): Show | 101 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.76+9972_76+9974del others(3): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963699 | ||||||
| chr3:93963758
|
A | T | 1 | a0001c0001t0001g0299 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.76+9916T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963758 | ||||||
| chr3:93963825
|
C | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.76+9849G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963825 | ||||||
| chr3:93963877
|
C | G | 4 | a0001c0001t0002g0003a0001c0001t0002g0191a0001c0001t0002g0220others(1): Show | 5 | HG02486.hp2 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+9797G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93963877 | ||||||
| chr3:93964504
|
A | C | 2 | a0001c0002t0001g0137a0001c0002t0001g0226 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.76+9170T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93964504 | ||||||
| chr3:93964549
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.76+9125C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93964549 | ||||||
| chr3:93964799
|
C | G | 1 | a0001c0002t0001g0247 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.76+8875G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93964799 | ||||||
| chr3:93964932
|
T | TAAGAATC others(2421): Show |
1 | a0001c0001t0002g0102 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.76+8741_76+8742ins others(2428): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93964932 | ||||||
| chr3:93965094
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+8580G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965094 | ||||||
| chr3:93965111
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.76+8563C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965111 | ||||||
| chr3:93965166
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.76+8508G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965166 | ||||||
| chr3:93965173
|
A | G | 1 | a0001c0002t0001g0175 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.76+8501T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965173 | ||||||
| chr3:93965189
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.76+8485G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965189 | ||||||
| chr3:93965291
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.76+8383G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965291 | ||||||
| chr3:93965314
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76+8360G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965314 | ||||||
| chr3:93965559
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76+8115G>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965559 | ||||||
| chr3:93965643
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.76+8031A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93965643 | ||||||
| chr3:93966075
|
G | T | 1 | a0001c0001t0001g0299 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.76+7599C>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966075 | ||||||
| chr3:93966190
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.76+7484C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966190 | ||||||
| chr3:93966291
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.76+7383T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966291 | ||||||
| chr3:93966317
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.76+7357G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966317 | ||||||
| chr3:93966809
|
C | CA | 9 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0286others(6): Show | 9 | HG01884.hp2 HG02738.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.76+6864dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966809 | ||||||
| chr3:93966825
|
A | G | 3 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0009g0129 | 3 | HG00438.hp1 NA19043.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.76+6849T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966825 | ||||||
| chr3:93966881
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.76+6793G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966881 | ||||||
| chr3:93966968
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76+6706C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93966968 | ||||||
| chr3:93967009
|
T | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0094others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+6665A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93967009 | ||||||
| chr3:93967164
|
A | G | 1 | a0001c0002t0001g0174 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.76+6510T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93967164 | ||||||
| chr3:93967240
|
C | T | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01884.hp1 HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.76+6434G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93967240 | ||||||
| chr3:93967286
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.76+6388G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93967286 | ||||||
| chr3:93967825
|
G | C | 3 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0167 | 3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76+5849C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93967825 | ||||||
| chr3:93968578
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.76+5096A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93968578 | ||||||
| chr3:93968743
|
TA | T | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 31 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.76+4930delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93968743 | ||||||
| chr3:93968999
|
T | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0102a0001c0001t0002g0104 | 3 | HG00438.hp1 HG02080.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.76+4675A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93968999 | ||||||
| chr3:93969082
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.76+4592C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93969082 | ||||||
| chr3:93969122
|
C | CT | 34 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0066others(31): Show | 34 | HG00609.hp2 HG00621.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.76+4551dupA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93969122 | ||||||
| chr3:93969287
|
A | G | 1 | a0001c0002t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.76+4387T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93969287 | ||||||
| chr3:93969553
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76+4121T>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93969553 | ||||||
| chr3:93969667
|
G | A | 140 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(137): Show | 141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.76+4007C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93969667 | ||||||
| chr3:93969828
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0064 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.76+3846C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93969828 | ||||||
| chr3:93970174
|
G | C | 1 | a0001c0002t0001g0267 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.76+3500C>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970174 | ||||||
| chr3:93970194
|
G | A | 1 | a0002c0004t0001g0219 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.76+3480C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970194 | ||||||
| chr3:93970514
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.76+3160T>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970514 | ||||||
| chr3:93970674
|
ATC | A | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 31 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.76+2998_76+2999del others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970674 | ||||||
| chr3:93970911
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.76+2763A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970911 | ||||||
| chr3:93970953
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0306a0001c0001t0007g0305 | 3 | HG02922.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.76+2721C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970953 | ||||||
| chr3:93970991
|
AT | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0220a0001c0001t0002g0221 | 4 | HG02486.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+2682delA | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970991 | ||||||
| chr3:93970993
|
T | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76+2681A>C | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93970993 | ||||||
| chr3:93971024
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.76+2650C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971024 | ||||||
| chr3:93971153
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG02970.hp2 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+2521G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971153 | ||||||
| chr3:93971354
|
TCTAAATA others(5): Show |
T | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.76+2308_76+2319del others(12): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971354 | ||||||
| chr3:93971355
|
C | CTAAA | 5 | a0001c0001t0001g0105a0001c0001t0001g0197a0001c0001t0001g0261others(2): Show | 5 | HG00438.hp1 HG02572.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+2315_76+2318dup others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971355 | ||||||
| chr3:93971355
|
CTAAA | C | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(197): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.76+2315_76+2318del others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971355 | ||||||
| chr3:93971355
|
CTAAATAA others(1): Show |
C | 22 | a0001c0001t0001g0038a0001c0001t0001g0084a0001c0001t0001g0140others(19): Show | 23 | HG02280.hp1 HG02486.hp1 HG02615.hp1 others(20): Show |
intron_variant | MODIFIER | c.76+2311_76+2318del others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971355 | ||||||
| chr3:93971355
|
CTAAATAA others(5): Show |
C | 51 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 52 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.76+2307_76+2318del others(12): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971355 | ||||||
| chr3:93971355
|
CTAAATAA others(17): Show |
C | 1 | a0008c0011t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76+2295_76+2318del others(24): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971355 | ||||||
| chr3:93971355
|
CTAAATAA others(21): Show |
C | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0040 | 3 | HG01168.hp2 HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.76+2291_76+2318del others(28): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971355 | ||||||
| chr3:93971383
|
ATAAATAA others(15): Show |
A | 1 | a0001c0001t0002g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.76+2269_76+2290del others(22): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971383 | ||||||
| chr3:93971550
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.76+2124C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971550 | ||||||
| chr3:93971558
|
G | A | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 31 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.76+2116C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971558 | ||||||
| chr3:93971627
|
C | CCA | 58 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(55): Show | 58 | HG01106.hp1 HG01168.hp2 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.76+2045_76+2046dup others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
C | CCACA | 76 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0140others(73): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.76+2043_76+2046dup others(4): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
C | CCACACA | 42 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0200others(39): Show | 43 | HG00558.hp1 HG01071.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.76+2041_76+2046dup others(6): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
C | CCACACAC others(1): Show |
32 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0291others(29): Show | 32 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.76+2039_76+2046dup others(8): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
C | CCACACAC others(3): Show |
13 | a0001c0001t0001g0295a0001c0002t0001g0245a0001c0002t0001g0246others(10): Show | 13 | HG00408.hp2 HG01496.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.76+2037_76+2046dup others(10): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
C | CCACACAC others(5): Show |
4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02071.hp2 HG02132.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+2035_76+2046dup others(12): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
CCA | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00140.hp2 HG01074.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.76+2045_76+2046del others(2): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971627
|
CCACACAC others(11): Show |
C | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.76+2029_76+2046del others(18): Show |
PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971627 | ||||||
| chr3:93971672
|
T | A | 1 | a0001c0002t0001g0260 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.76+2002A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971672 | ||||||
| chr3:93971672
|
T | C | 1 | a0001c0002t0001g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.76+2002A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971672 | ||||||
| chr3:93971687
|
C | A | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76+1987G>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93971687 | ||||||
| chr3:93972003
|
T | A | 7 | a0001c0002t0001g0263a0001c0002t0001g0264a0001c0002t0001g0265others(4): Show | 7 | HG00609.hp1 NA18612.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.76+1671A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972003 | ||||||
| chr3:93972160
|
T | C | 32 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(29): Show | 32 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.76+1514A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972160 | ||||||
| chr3:93972255
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.76+1419C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972255 | ||||||
| chr3:93972315
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76+1359T>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972315 | ||||||
| chr3:93972332
|
T | C | 1 | a0001c0002t0001g0296 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.76+1342A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972332 | ||||||
| chr3:93972367
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76+1307A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972367 | ||||||
| chr3:93972433
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.76+1241A>G | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972433 | ||||||
| chr3:93972631
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0064 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.76+1043C>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972631 | ||||||
| chr3:93972684
|
C | CA | 12 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0301others(9): Show | 12 | HG00408.hp1 HG00438.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.76+989dupT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972684 | ||||||
| chr3:93972684
|
CA | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 59 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.76+989delT | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93972684 | ||||||
| chr3:93973323
|
C | T | 1 | a0001c0002t0001g0007 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.76+351G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93973323 | ||||||
| chr3:93973451
|
T | A | 2 | a0001c0007t0002g0311a0001c0013t0002g0310 | 2 | NA18956.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.76+223A>T | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93973451 | ||||||
| chr3:93973498
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.76+176G>A | PROS1 | ENSG00000184500.16 | transcript | ENST00000394236.9 | protein_coding | 1/14 | chr3 | 93973498 |