Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11234 |
|---|---|
| ensemblid | ENSG00000110756.18 |
| hgncid | 17022 |
| symbol | HPS5 |
| name | HPS5 biogenesis of lysosomal organelles complex 2 subunit 2 |
| refseq_nuc | NM_181507.2 |
| refseq_prot | NP_852608.1 |
| ensembl_nuc | ENST00000349215.8 |
| ensembl_prot | ENSP00000265967.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 18278676 |
| end | 18322140 |
| strand | - |
| ver | v1.2 |
| region | chr11:18278676-18322140 |
| region5000 | chr11:18273676-18327140 |
| regionname0 | HPS5_chr11_18278676_18322140 |
| regionname5000 | HPS5_chr11_18273676_18327140 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1129 | 295 | 81 | 50 | 128 | 10 | 24 | 99 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002 | 0/0 | 1129 | 56 | 14 | 10 | 28 | 3 | 1 | 22 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0003 | 0/0 | 1129 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0004 | 0/0 | 1129 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0005 | 0/0 | 1129 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0006 | 0/0 | 1129 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0007 | 0/0 | 1129 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0008 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0009 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0010 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0011 | 0/0 | 1129 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0012 | 0/0 | 1129 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0013 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0014 | 0/0 | 1129 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0015 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0016 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0017 | 0/0 | 1129 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3390 | 232 | 53 | 35 | 120 | 9 | 15 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0002 | 0/0 | 3390 | 55 | 14 | 9 | 28 | 3 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0003 | 1/1 | 3390 | 51 | 17 | 15 | 8 | 1 | 8 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0004 | 0/0 | 3390 | 9 | 9 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0005 | 0/0 | 3390 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0006 | 0/0 | 3390 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0007 | 0/0 | 3390 | 2 | 0 | 0 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0008 | 0/0 | 3390 | 2 | 0 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0009 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0010 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0011 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0012 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0013 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0014 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0015 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0016 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0017 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0018 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0019 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0020 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0021 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0022 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0023 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| c0024 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1451 | 119 | 49 | 15 | 42 | 1 | 10 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0002 | 0/0 | 1451 | 112 | 15 | 15 | 72 | 2 | 8 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0003 | 0/0 | 1451 | 89 | 0 | 26 | 43 | 9 | 11 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0004 | 0/0 | 1451 | 20 | 13 | 4 | 0 | 2 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0005 | 0/0 | 1451 | 9 | 7 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0006 | 0/0 | 1451 | 6 | 6 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0007 | 0/0 | 1451 | 5 | 0 | 0 | 5 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0008 | 0/0 | 1451 | 4 | 3 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0009 | 0/0 | 1451 | 3 | 2 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0010 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0011 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0012 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0013 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| t0014 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0002 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3390 | 232 | 53 | 35 | 120 | 9 | 15 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0003 | 1/1 | 3390 | 51 | 17 | 15 | 8 | 1 | 8 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0004 | 0/0 | 3390 | 9 | 9 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0010 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0014 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0018 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0002 | 0/0 | 3390 | 55 | 14 | 9 | 28 | 3 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0024 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0003c0008 | 0/0 | 3390 | 2 | 0 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0003c0019 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0004c0005 | 0/0 | 3390 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0005c0007 | 0/0 | 3390 | 2 | 0 | 0 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0006c0006 | 0/0 | 3390 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0007c0009 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0008c0023 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0009c0013 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0010c0020 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0011c0021 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0012c0017 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0013c0012 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0014c0016 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0015c0015 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0016c0011 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0017c0022 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4840 | 70 | 33 | 4 | 32 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0002 | 0/0 | 4840 | 57 | 3 | 5 | 44 | 1 | 4 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0003 | 0/0 | 4840 | 76 | 0 | 23 | 37 | 6 | 10 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0004 | 0/0 | 4840 | 3 | 1 | 0 | 0 | 2 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0005 | 0/0 | 4840 | 9 | 7 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0006 | 0/0 | 4840 | 5 | 5 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0007 | 0/0 | 4840 | 5 | 0 | 0 | 5 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0008 | 0/0 | 4840 | 4 | 3 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0010 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0011 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0001t0013 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0003t0001 | 1/1 | 4840 | 31 | 4 | 8 | 8 | 1 | 8 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0003t0003 | 0/0 | 4840 | 2 | 0 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0003t0004 | 0/0 | 4840 | 15 | 11 | 4 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0003t0009 | 0/0 | 4840 | 3 | 2 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0004t0001 | 0/0 | 4840 | 9 | 9 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0010t0001 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0014t0001 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0001c0018t0002 | 0/0 | 4840 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0002t0001 | 0/0 | 4840 | 2 | 1 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0002t0002 | 0/0 | 4840 | 47 | 11 | 9 | 25 | 1 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0002t0003 | 0/0 | 4840 | 4 | 0 | 0 | 2 | 2 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0002t0004 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0002t0014 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0002c0024t0002 | 0/0 | 4840 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0003c0008t0001 | 0/0 | 4840 | 2 | 0 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0003c0019t0003 | 0/0 | 4840 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0004c0005t0003 | 0/0 | 4840 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0005c0007t0002 | 0/0 | 4840 | 2 | 0 | 0 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0006c0006t0002 | 0/0 | 4840 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0007c0009t0004 | 0/0 | 4840 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0008c0023t0002 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0009c0013t0001 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0010c0020t0006 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0011c0021t0001 | 0/0 | 4840 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0012c0017t0003 | 0/0 | 4840 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0013c0012t0002 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0014c0016t0003 | 0/0 | 4840 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0015c0015t0012 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0016c0011t0003 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| a0017c0022t0001 | 0/0 | 4840 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | copy fasta | chr11 | 18273676 | 18327140 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0006g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0008g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0011g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0001t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0009g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0009g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0003t0009g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0010t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0014t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0001c0018t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0002t0014g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0002c0024t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0003c0008t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0003c0008t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0003c0019t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0004c0005t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0004c0005t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0004c0005t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0005c0007t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0005c0007t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0006c0006t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0006c0006t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0007c0009t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0008c0023t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0009c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0010c0020t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0011c0021t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0012c0017t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0013c0012t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0014c0016t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0015c0015t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0016c0011t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| a0017c0022t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0189 | EUR | GBR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0100 | EUR | GBR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0142 | EUR | GBR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | FIN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0025 | EUR | FIN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0159 | EUR | FIN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0125 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0185 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00741 | hp1 | a0011 | c0021 | t0001 | g0048 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0321 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01074 | hp2 | a0001 | c0003 | t0004 | g0071 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0046 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01106 | hp2 | a0014 | c0016 | t0003 | g0162 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01175 | hp2 | a0001 | c0003 | t0004 | g0069 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01243 | hp2 | a0001 | c0003 | t0009 | g0342 | AMR | PUR | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0042 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01261 | hp2 | a0001 | c0003 | t0003 | g0172 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0031 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01361 | hp2 | a0001 | c0003 | t0004 | g0070 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0306 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01496 | hp1 | a0001 | c0003 | t0004 | g0061 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0049 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0225 | EUR | IBS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01516 | hp2 | a0012 | c0017 | t0003 | g0151 | EUR | IBS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0222 | EUR | IBS | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01884 | hp1 | a0010 | c0020 | t0006 | g0346 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0059 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0231 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01891 | hp2 | a0001 | c0003 | t0009 | g0344 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01934 | hp1 | a0003 | c0008 | t0001 | g0052 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0228 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0211 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01978 | hp1 | a0002 | c0024 | t0002 | g0219 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01981 | hp2 | a0003 | c0008 | t0001 | g0050 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0205 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02135 | hp1 | a0004 | c0005 | t0003 | g0340 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0095 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0073 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | CDX | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CDX | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CDX | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | CDX | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0345 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0215 | AMR | PEL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0298 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0297 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0063 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02602 | hp2 | a0003 | c0019 | t0003 | g0184 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0300 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0028 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02622 | hp2 | a0002 | c0002 | t0014 | g0341 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0226 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02647 | hp2 | a0001 | c0014 | t0001 | g0334 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0296 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0299 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0305 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0034 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02738 | hp1 | a0007 | c0009 | t0004 | g0067 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0294 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0302 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02970 | hp2 | a0001 | c0003 | t0004 | g0029 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0044 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0064 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0212 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0216 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0055 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0203 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0060 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0020 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0043 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0304 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0348 | AFR | ESN | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0308 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0301 | AFR | GWD | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0241 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | STU | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03688 | hp2 | a0001 | c0018 | t0002 | g0188 | SAS | STU | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0236 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03834 | hp1 | a0005 | c0007 | t0002 | g0227 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0040 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0039 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03942 | hp2 | a0005 | c0007 | t0002 | g0223 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0023 | SAS | BEB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0318 | SAS | STU | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18522 | hp1 | a0001 | c0003 | t0009 | g0343 | AFR | YRI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | CHB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | YRI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | YRI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18943 | hp1 | a0001 | c0001 | t0011 | g0089 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18943 | hp2 | a0006 | c0006 | t0002 | g0258 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18944 | hp2 | a0009 | c0013 | t0001 | g0145 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0018 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18980 | hp2 | a0004 | c0005 | t0003 | g0102 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18984 | hp2 | a0016 | c0011 | t0003 | g0179 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18987 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18988 | hp1 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18989 | hp1 | a0006 | c0006 | t0002 | g0254 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18989 | hp2 | a0004 | c0005 | t0003 | g0111 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18992 | hp2 | a0001 | c0001 | t0007 | g0242 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0200 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0347 | AFR | LWK | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19030 | hp2 | a0001 | c0003 | t0004 | g0062 | AFR | LWK | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | LWK | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19043 | hp2 | a0013 | c0012 | t0002 | g0213 | AFR | LWK | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19066 | hp2 | a0008 | c0023 | t0002 | g0197 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19072 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19075 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0099 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0335 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | YRI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0303 | AFR | YRI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0218 | EUR | TSI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0123 | EUR | TSI | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA20905 | hp1 | a0017 | c0022 | t0001 | g0041 | SAS | GIH | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | GIH | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0232 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0030 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02109 | hp2 | a0015 | c0015 | t0012 | g0072 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0323 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0230 | AFR | ACB | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03471 | hp1 | a0001 | c0003 | t0004 | g0065 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | USA | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| HG06807 | hp2 | a0001 | c0003 | t0004 | g0066 | AFR | USA | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA20300 | hp2 | a0001 | c0010 | t0001 | g0108 | AFR | USA | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | LWK | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | LWK | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0024 | REF | REF | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0057 | REF | REF | HPS5_chr11_18273676_18327140 | HPS5 | chr11 | 18273676 | 18327140 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18281986
|
G | A | 1 | a0012 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.3293C>T | p.Thr1098Ile | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/23 | 3537/4840 | 3293/3390 | 1098/1129 | chr11 | 18281986 | ||
| chr11:18282050
|
G | A | 1 | a0006 | 2 | NA18943.hp2 NA18989.hp1 |
missense_variant | MODERATE | c.3229C>T | p.Arg1077Trp | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/23 | 3473/4840 | 3229/3390 | 1077/1129 | chr11 | 18282050 | ||
| chr11:18282062
|
T | C | 1 | a0013 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3217A>G | p.Met1073Val | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/23 | 3461/4840 | 3217/3390 | 1073/1129 | chr11 | 18282062 | ||
| chr11:18283807
|
C | T | 1 | a0014 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.3046G>A | p.Glu1016Lys | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/23 | 3290/4840 | 3046/3390 | 1016/1129 | chr11 | 18283807 | ||
| chr11:18283808
|
C | T | 1 | a0011 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.3045G>A | p.Met1015Ile | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/23 | 3289/4840 | 3045/3390 | 1015/1129 | chr11 | 18283808 | ||
| chr11:18287917
|
G | A | 1 | a0003 | 3 | HG01934.hp1 HG01981.hp2 HG02602.hp2 |
missense_variant | MODERATE | c.2537C>T | p.Pro846Leu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 17/23 | 2781/4840 | 2537/3390 | 846/1129 | chr11 | 18287917 | ||
| chr11:18291700
|
C | T | 1 | a0015 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2182G>A | p.Ala728Thr | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/23 | 2426/4840 | 2182/3390 | 728/1129 | chr11 | 18291700 | ||
| chr11:18291982
|
C | T | 1 | a0004 | 3 | HG02135.hp1 NA18980.hp2 NA18989.hp2 |
missense_variant | MODERATE | c.1900G>A | p.Glu634Lys | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/23 | 2144/4840 | 1900/3390 | 634/1129 | chr11 | 18291982 | ||
| chr11:18295050
|
G | A | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1754C>T | p.Ser585Leu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/23 | 1998/4840 | 1754/3390 | 585/1129 | chr11 | 18295050 | ||
| chr11:18296097
|
C | T | 1 | a0009 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.1536G>A | p.Met512Ile | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 13/23 | 1780/4840 | 1536/3390 | 512/1129 | chr11 | 18296097 | ||
| chr11:18296833
|
A | T | 1 | a0016 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1475T>A | p.Leu492Gln | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/23 | 1719/4840 | 1475/3390 | 492/1129 | chr11 | 18296833 | ||
| chr11:18297633
|
G | T | 3 | a0002a0005a0008 | 59 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
missense_variant | MODERATE | c.1249C>A | p.Leu417Met | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 11/23 | 1493/4840 | 1249/3390 | 417/1129 | chr11 | 18297633 | ||
| chr11:18298919
|
T | C | 1 | a0017 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1037A>G | p.Asn346Ser | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/23 | 1281/4840 | 1037/3390 | 346/1129 | chr11 | 18298919 | ||
| chr11:18300855
|
G | C | 1 | a0005 | 2 | HG03834.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.958C>G | p.Gln320Glu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/23 | 1202/4840 | 958/3390 | 320/1129 | chr11 | 18300855 | ||
| chr11:18310871
|
T | C | 1 | a0008 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.347A>G | p.Tyr116Cys | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/23 | 591/4840 | 347/3390 | 116/1129 | chr11 | 18310871 | ||
| chr11:18310873
|
C | T | 1 | a0007 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.345G>A | p.Met115Ile | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/23 | 589/4840 | 345/3390 | 115/1129 | chr11 | 18310873 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18282015
|
G | A | 1 | a0001c0018 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.3264C>T | p.Ala1088Ala | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/23 | 3508/4840 | 3264/3390 | 1088/1129 | chr11 | 18282015 | ||
| chr11:18291773
|
A | G | 1 | a0001c0014 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.2109T>C | p.Asp703Asp | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/23 | 2353/4840 | 2109/3390 | 703/1129 | chr11 | 18291773 | ||
| chr11:18296832
|
C | T | 1 | a0013c0012 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1476G>A | p.Leu492Leu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/23 | 1720/4840 | 1476/3390 | 492/1129 | chr11 | 18296832 | ||
| chr11:18306137
|
G | T | 19 | a0001c0001a0001c0004a0001c0010others(16): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
splice_region_variant&synonymous_variant | LOW | c.822C>A | p.Leu274Leu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/23 | 1066/4840 | 822/3390 | 274/1129 | chr11 | 18306137 | ||
| chr11:18308960
|
C | T | 1 | a0001c0010 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.597G>A | p.Leu199Leu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/23 | 841/4840 | 597/3390 | 199/1129 | chr11 | 18308960 | ||
| chr11:18310909
|
T | C | 1 | a0002c0024 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.309A>G | p.Glu103Glu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/23 | 553/4840 | 309/3390 | 103/1129 | chr11 | 18310909 | ||
| chr11:18311994
|
A | G | 1 | a0001c0004 | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.139T>C | p.Leu47Leu | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/23 | 383/4840 | 139/3390 | 47/1129 | chr11 | 18311994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18278691
|
A | G | 1 | a0015c0015t0012 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1191T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 1191 | chr11 | 18278691 | |||||
| chr11:18278814
|
A | T | 2 | a0001c0001t0005a0001c0001t0008 | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1068T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 1068 | chr11 | 18278814 | |||||
| chr11:18279078
|
G | A | 5 | a0001c0001t0004a0001c0003t0004a0001c0003t0009others(2): Show | 23 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*804C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 804 | chr11 | 18279078 | |||||
| chr11:18279180
|
T | A | 1 | a0001c0001t0005 | 9 | HG01070.hp2 HG01433.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*702A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 702 | chr11 | 18279180 | |||||
| chr11:18279407
|
G | A | 14 | a0001c0001t0002a0001c0001t0004a0001c0003t0004others(11): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*475C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 475 | chr11 | 18279407 | |||||
| chr11:18279418
|
G | T | 8 | a0001c0001t0003a0001c0003t0003a0002c0002t0003others(5): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*464C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 464 | chr11 | 18279418 | |||||
| chr11:18279439
|
A | T | 2 | a0001c0001t0005a0001c0001t0008 | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*443T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 443 | chr11 | 18279439 | |||||
| chr11:18279520
|
C | T | 1 | a0001c0001t0007 | 5 | HG00609.hp2 NA18956.hp1 NA18992.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*362G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 362 | chr11 | 18279520 | |||||
| chr11:18279582
|
A | G | 14 | a0001c0001t0002a0001c0001t0004a0001c0003t0004others(11): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*300T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 300 | chr11 | 18279582 | |||||
| chr11:18279583
|
G | A | 14 | a0001c0001t0002a0001c0001t0004a0001c0003t0004others(11): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*299C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 299 | chr11 | 18279583 | |||||
| chr11:18279606
|
A | C | 1 | a0001c0001t0011 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*276T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 276 | chr11 | 18279606 | |||||
| chr11:18279827
|
G | A | 1 | a0001c0001t0013 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 23/23 | 55 | chr11 | 18279827 | |||||
| chr11:18321971
|
T | C | 1 | a0002c0002t0014 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/23 | 4113 | chr11 | 18321971 | |||||
| chr11:18321978
|
A | C | 1 | a0001c0001t0010 | 1 | NA18979.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/23 | 4120 | chr11 | 18321978 | |||||
| chr11:18321987
|
G | C | 1 | a0001c0003t0009 | 3 | HG01243.hp2 HG01891.hp2 NA18522.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/23 | chr11 | 18321987 | ||||||
| chr11:18322038
|
G | A | 2 | a0001c0001t0006a0010c0020t0006 | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-142C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/23 | chr11 | 18322038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18280058
|
T | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0016others(134): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3330-116A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280058 | ||||||
| chr11:18280110
|
A | C | 2 | a0001c0001t0007g0125a0001c0001t0007g0242 | 2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3330-168T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280110 | ||||||
| chr11:18280286
|
C | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0128 | 2 | NA18939.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3330-344G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280286 | ||||||
| chr11:18280293
|
T | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0016others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.3330-351A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280293 | ||||||
| chr11:18280341
|
C | G | 2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3330-399G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280341 | ||||||
| chr11:18280367
|
A | G | 2 | a0001c0003t0001g0021a0001c0003t0001g0026 | 2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.3330-425T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280367 | ||||||
| chr11:18280368
|
A | G | 34 | a0002c0002t0002g0005a0002c0002t0002g0058a0002c0002t0002g0201others(31): Show | 36 | HG00423.hp2 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.3330-426T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280368 | ||||||
| chr11:18280513
|
T | C | 1 | a0013c0012t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3330-571A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280513 | ||||||
| chr11:18280794
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3330-852C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280794 | ||||||
| chr11:18280934
|
A | G | 2 | a0002c0002t0002g0232a0002c0024t0002g0219 | 2 | HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.3330-992T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280934 | ||||||
| chr11:18280941
|
AG | A | 101 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0090others(98): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3330-1000delC | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280941 | ||||||
| chr11:18280979
|
AATACCAC others(10): Show |
A | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3329+954_3329+970d others(19): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280979 | ||||||
| chr11:18280999
|
T | C | 11 | a0001c0001t0005g0015a0001c0001t0005g0306a0001c0001t0005g0307others(8): Show | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.3329+951A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18280999 | ||||||
| chr11:18281082
|
A | AT | 69 | a0001c0001t0001g0097a0001c0001t0001g0164a0001c0001t0002g0012others(66): Show | 75 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.3329+867dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281082 | ||||||
| chr11:18281082
|
AT | A | 6 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0338others(3): Show | 6 | HG00642.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3329+867delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281082 | ||||||
| chr11:18281254
|
C | T | 344 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(341): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.3329+696G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281254 | ||||||
| chr11:18281255
|
A | AT | 41 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(38): Show | 42 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.3329+694dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281255 | ||||||
| chr11:18281255
|
A | T | 1 | a0001c0001t0005g0322 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3329+695T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281255 | ||||||
| chr11:18281255
|
AT | A | 7 | a0001c0001t0001g0076a0001c0001t0002g0250a0001c0001t0006g0017others(4): Show | 8 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3329+694delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281255 | ||||||
| chr11:18281258
|
T | A | 34 | a0002c0002t0002g0005a0002c0002t0002g0058a0002c0002t0002g0201others(31): Show | 36 | HG00423.hp2 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.3329+692A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281258 | ||||||
| chr11:18281273
|
T | A | 1 | a0001c0001t0002g0265 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3329+677A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281273 | ||||||
| chr11:18281314
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0006g0017a0001c0001t0006g0345others(3): Show | 7 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3329+636C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281314 | ||||||
| chr11:18281317
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3329+633G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281317 | ||||||
| chr11:18281383
|
C | G | 1 | a0001c0001t0006g0348 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3329+567G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281383 | ||||||
| chr11:18281384
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3329+566C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281384 | ||||||
| chr11:18281385
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3329+565A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281385 | ||||||
| chr11:18281421
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3329+529C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281421 | ||||||
| chr11:18281493
|
G | A | 1 | a0002c0002t0002g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3329+457C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281493 | ||||||
| chr11:18281558
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3329+392G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281558 | ||||||
| chr11:18281575
|
CT | C | 263 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0016others(260): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.3329+374delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281575 | ||||||
| chr11:18281622
|
T | C | 101 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0090others(98): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3329+328A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281622 | ||||||
| chr11:18281695
|
C | T | 1 | a0001c0003t0001g0053 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3329+255G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281695 | ||||||
| chr11:18281805
|
C | T | 5 | a0001c0001t0007g0099a0001c0001t0007g0125a0001c0001t0007g0171others(2): Show | 5 | HG00609.hp2 NA18956.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.3329+145G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281805 | ||||||
| chr11:18281857
|
C | T | 101 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0090others(98): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3329+93G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281857 | ||||||
| chr11:18281882
|
C | T | 2 | a0002c0002t0002g0191a0002c0002t0002g0192 | 2 | NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.3329+68G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 22/22 | chr11 | 18281882 | ||||||
| chr11:18282431
|
C | CT | 43 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0207others(40): Show | 48 | HG00423.hp2 HG00639.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.3059-212dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18282431 | ||||||
| chr11:18282587
|
C | T | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3059-367G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18282587 | ||||||
| chr11:18282747
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3059-527A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18282747 | ||||||
| chr11:18282854
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0313others(15): Show | 21 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.3059-634C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18282854 | ||||||
| chr11:18283125
|
T | A | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3058+670A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283125 | ||||||
| chr11:18283188
|
G | A | 1 | a0001c0001t0003g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3058+607C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283188 | ||||||
| chr11:18283193
|
G | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0309a0001c0001t0001g0310others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3058+602C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283193 | ||||||
| chr11:18283328
|
T | TA | 8 | a0001c0001t0004g0134a0001c0001t0004g0159a0001c0001t0004g0189others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.3058+466dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283328 | ||||||
| chr11:18283328
|
TA | T | 77 | a0001c0001t0001g0083a0001c0001t0001g0311a0001c0001t0001g0325others(74): Show | 83 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.3058+466delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283328 | ||||||
| chr11:18283511
|
T | TAAAACAA others(2782): Show |
1 | a0002c0002t0002g0224 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3058+283_3058+284i others(2791): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283511 | ||||||
| chr11:18283511
|
T | TAAAACAA others(2774): Show |
1 | a0002c0002t0002g0218 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3058+283_3058+284i others(2783): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283511 | ||||||
| chr11:18283511
|
T | TAAAACAA others(2800): Show |
1 | a0002c0002t0002g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3058+283_3058+284i others(2809): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283511 | ||||||
| chr11:18283511
|
T | TAAAACAA others(2801): Show |
1 | a0002c0002t0002g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3058+283_3058+284i others(2810): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283511 | ||||||
| chr11:18283712
|
G | C | 1 | a0006c0006t0002g0254 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3058+83C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283712 | ||||||
| chr11:18283786
|
T | C | 35 | a0001c0001t0004g0134a0001c0001t0004g0159a0001c0001t0004g0189others(32): Show | 37 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.3058+9A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 21/22 | chr11 | 18283786 | ||||||
| chr11:18284000
|
C | T | 1 | a0001c0001t0003g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2952-99G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284000 | ||||||
| chr11:18284061
|
C | T | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2952-160G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284061 | ||||||
| chr11:18284076
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2952-175T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284076 | ||||||
| chr11:18284138
|
A | G | 2 | a0001c0001t0003g0106a0001c0001t0003g0115 | 2 | HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2952-237T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284138 | ||||||
| chr11:18284167
|
G | GA | 8 | a0001c0001t0002g0260a0001c0001t0002g0275a0001c0001t0002g0284others(5): Show | 8 | HG01978.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2952-267dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284167 | ||||||
| chr11:18284174
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2952-273T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284174 | ||||||
| chr11:18284210
|
G | C | 23 | a0001c0001t0004g0134a0001c0001t0004g0159a0001c0001t0004g0189others(20): Show | 23 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2952-309C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284210 | ||||||
| chr11:18284725
|
G | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0008others(76): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2951+621C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284725 | ||||||
| chr11:18284852
|
G | A | 94 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0175others(91): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.2951+494C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18284852 | ||||||
| chr11:18285142
|
T | TA | 14 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0317others(11): Show | 14 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2951+203dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18285142 | ||||||
| chr11:18285142
|
TA | T | 9 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0168others(6): Show | 9 | HG03041.hp2 NA18959.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.2951+203delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18285142 | ||||||
| chr11:18285288
|
A | C | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2951+58T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 20/22 | chr11 | 18285288 | ||||||
| chr11:18285498
|
T | C | 59 | a0001c0001t0001g0207a0001c0001t0002g0012a0001c0001t0002g0013others(56): Show | 61 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2838-39A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18285498 | ||||||
| chr11:18285598
|
A | C | 1 | a0017c0022t0001g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2838-139T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18285598 | ||||||
| chr11:18285739
|
CT | C | 10 | a0001c0001t0005g0323a0001c0004t0001g0296a0001c0004t0001g0298others(7): Show | 10 | HG02451.hp1 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2838-281delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18285739 | ||||||
| chr11:18285881
|
A | C | 1 | a0001c0001t0003g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2838-422T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18285881 | ||||||
| chr11:18286028
|
C | A | 275 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(272): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2837+563G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286028 | ||||||
| chr11:18286371
|
C | G | 2 | a0002c0002t0002g0058a0002c0002t0002g0294 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2837+220G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286371 | ||||||
| chr11:18286427
|
C | T | 1 | a0004c0005t0003g0111 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2837+164G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286427 | ||||||
| chr11:18286452
|
T | TA | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2837+138dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286452 | ||||||
| chr11:18286493
|
G | T | 7 | a0001c0003t0004g0060a0001c0003t0004g0061a0001c0003t0004g0062others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2837+98C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286493 | ||||||
| chr11:18286521
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2837+70C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286521 | ||||||
| chr11:18286534
|
C | A | 10 | a0001c0001t0003g0009a0001c0001t0003g0117a0001c0001t0003g0122others(7): Show | 11 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2837+57G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286534 | ||||||
| chr11:18286541
|
C | CA | 12 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0325others(9): Show | 15 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2837+49dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286541 | ||||||
| chr11:18286547
|
A | C | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2837+44T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 19/22 | chr11 | 18286547 | ||||||
| chr11:18286877
|
A | G | 1 | a0001c0001t0006g0345 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2718-167T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18286877 | ||||||
| chr11:18286910
|
G | GA | 146 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.2718-201dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18286910 | ||||||
| chr11:18287015
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2718-305T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18287015 | ||||||
| chr11:18287065
|
T | C | 53 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(50): Show | 59 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2718-355A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18287065 | ||||||
| chr11:18287150
|
C | T | 1 | a0001c0003t0004g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2717+385G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18287150 | ||||||
| chr11:18287196
|
G | A | 1 | a0001c0003t0001g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2717+339C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18287196 | ||||||
| chr11:18287509
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2717+26C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 18/22 | chr11 | 18287509 | ||||||
| chr11:18287704
|
C | G | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2562-14G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 17/22 | chr11 | 18287704 | ||||||
| chr11:18288021
|
A | G | 2 | a0001c0001t0005g0307a0001c0001t0005g0308 | 2 | HG02818.hp1 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.2441-8T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288021 | ||||||
| chr11:18288153
|
A | G | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2441-140T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288153 | ||||||
| chr11:18288167
|
TAAA | T | 53 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(50): Show | 59 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2441-157_2441-155d others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288167 | ||||||
| chr11:18288512
|
G | A | 345 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(342): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2441-499C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288512 | ||||||
| chr11:18288596
|
TA | T | 54 | a0001c0001t0003g0113a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2441-584delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288596 | ||||||
| chr11:18288734
|
C | CTCTG | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2441-722_2441-721i others(6): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288734 | ||||||
| chr11:18288734
|
C | CTG | 20 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0003g0096others(17): Show | 22 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.2441-723_2441-722d others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288734 | ||||||
| chr11:18288734
|
C | CTGTG | 262 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(259): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2441-725_2441-722d others(6): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288734 | ||||||
| chr11:18288734
|
C | CTGTGTG | 7 | a0001c0001t0001g0084a0001c0001t0002g0243a0001c0001t0003g0086others(4): Show | 7 | HG02615.hp2 HG03710.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.2441-727_2441-722d others(8): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288734 | ||||||
| chr11:18288734
|
CTGTG | C | 3 | a0001c0003t0009g0342a0001c0003t0009g0343a0001c0003t0009g0344 | 3 | HG01243.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2441-725_2441-722d others(6): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288734 | ||||||
| chr11:18288765
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2441-752G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288765 | ||||||
| chr11:18288865
|
C | T | 1 | a0013c0012t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2441-852G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288865 | ||||||
| chr11:18288902
|
T | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(158): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2441-889A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18288902 | ||||||
| chr11:18289033
|
C | T | 3 | a0001c0001t0003g0093a0001c0001t0003g0094a0001c0001t0003g0166 | 3 | HG01109.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2441-1020G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289033 | ||||||
| chr11:18289120
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2441-1107T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289120 | ||||||
| chr11:18289124
|
G | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(4): Show | 7 | HG01070.hp2 HG02145.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2441-1111C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289124 | ||||||
| chr11:18289198
|
T | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2441-1185A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289198 | ||||||
| chr11:18289303
|
C | T | 2 | a0001c0001t0006g0017a0001c0001t0006g0348 | 3 | HG02922.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2441-1290G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289303 | ||||||
| chr11:18289533
|
A | G | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2441-1520T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289533 | ||||||
| chr11:18289579
|
G | GA | 59 | a0001c0001t0001g0014a0001c0001t0001g0214a0001c0001t0001g0309others(56): Show | 66 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.2441-1567dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18289579 | ||||||
| chr11:18290060
|
G | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2440+1382C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18290060 | ||||||
| chr11:18290154
|
T | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2440+1288A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18290154 | ||||||
| chr11:18290402
|
C | A | 2 | a0001c0003t0001g0023a0001c0003t0001g0025 | 2 | HG00323.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2440+1040G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18290402 | ||||||
| chr11:18290753
|
T | C | 1 | a0013c0012t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2440+689A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18290753 | ||||||
| chr11:18290787
|
G | A | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2440+655C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18290787 | ||||||
| chr11:18290863
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2440+579T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18290863 | ||||||
| chr11:18291090
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(134): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2440+352G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18291090 | ||||||
| chr11:18291247
|
C | A | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2440+195G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18291247 | ||||||
| chr11:18291359
|
CT | C | 5 | a0001c0001t0002g0183a0001c0001t0003g0110a0001c0001t0003g0128others(2): Show | 5 | HG02155.hp1 HG02165.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440+82delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18291359 | ||||||
| chr11:18291391
|
A | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2440+51T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18291391 | ||||||
| chr11:18291406
|
G | A | 238 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(235): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2440+36C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 16/22 | chr11 | 18291406 | ||||||
| chr11:18292094
|
T | G | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1863-75A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292094 | ||||||
| chr11:18292190
|
T | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1863-171A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292190 | ||||||
| chr11:18292209
|
CT | C | 235 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(232): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1863-191delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292209 | ||||||
| chr11:18292350
|
T | G | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1863-331A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292350 | ||||||
| chr11:18292364
|
A | C | 292 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(289): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1863-345T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292364 | ||||||
| chr11:18292409
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1863-390C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292409 | ||||||
| chr11:18292486
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1862+413C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292486 | ||||||
| chr11:18292789
|
A | G | 1 | a0002c0002t0002g0239 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1862+110T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292789 | ||||||
| chr11:18292812
|
G | A | 3 | a0001c0001t0003g0100a0001c0001t0003g0130a0001c0001t0003g0178 | 3 | HG00099.hp2 HG00738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1862+87C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292812 | ||||||
| chr11:18292848
|
T | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | NA18959.hp2 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1862+51A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292848 | ||||||
| chr11:18292882
|
T | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1862+17A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 15/22 | chr11 | 18292882 | ||||||
| chr11:18292989
|
G | A | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-13C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18292989 | ||||||
| chr11:18293032
|
C | CTT | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1785-58_1785-57dup others(2): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293032 | ||||||
| chr11:18293113
|
C | T | 1 | a0001c0001t0003g0116 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1785-137G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293113 | ||||||
| chr11:18293204
|
TG | T | 12 | a0002c0002t0001g0198a0002c0002t0002g0003a0002c0002t0002g0004others(9): Show | 16 | HG02080.hp2 HG02083.hp2 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.1785-229delC | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293204 | ||||||
| chr11:18293238
|
C | T | 2 | a0001c0001t0005g0307a0001c0001t0005g0308 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1785-262G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293238 | ||||||
| chr11:18293318
|
A | G | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1785-342T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293318 | ||||||
| chr11:18293406
|
T | C | 3 | a0001c0001t0005g0306a0001c0001t0005g0320a0001c0001t0005g0321 | 3 | HG01070.hp2 HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1785-430A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293406 | ||||||
| chr11:18293439
|
G | A | 5 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0316others(2): Show | 5 | HG02451.hp2 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1785-463C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293439 | ||||||
| chr11:18293489
|
G | A | 1 | a0001c0001t0003g0318 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1785-513C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293489 | ||||||
| chr11:18293610
|
A | G | 1 | a0001c0003t0001g0046 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1785-634T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293610 | ||||||
| chr11:18293629
|
A | G | 3 | a0001c0001t0006g0017a0001c0001t0006g0347a0001c0001t0006g0348 | 4 | HG02922.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785-653T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293629 | ||||||
| chr11:18293743
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1785-767G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293743 | ||||||
| chr11:18293758
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1785-782C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293758 | ||||||
| chr11:18293870
|
A | G | 1 | a0001c0003t0001g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1785-894T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293870 | ||||||
| chr11:18293928
|
A | AC | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1785-953_1785-952i others(3): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18293928 | ||||||
| chr11:18294018
|
G | A | 11 | a0001c0001t0005g0015a0001c0001t0005g0306a0001c0001t0005g0307others(8): Show | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1784+1002C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294018 | ||||||
| chr11:18294242
|
T | G | 1 | a0002c0002t0002g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1784+778A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294242 | ||||||
| chr11:18294369
|
CCTTGACT others(11): Show |
C | 1 | a0001c0001t0003g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1784+633_1784+650d others(20): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294369 | ||||||
| chr11:18294398
|
G | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1784+622C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294398 | ||||||
| chr11:18294424
|
T | C | 1 | a0001c0001t0003g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1784+596A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294424 | ||||||
| chr11:18294443
|
T | A | 1 | a0013c0012t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1784+577A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294443 | ||||||
| chr11:18294702
|
T | C | 7 | a0001c0003t0004g0060a0001c0003t0004g0061a0001c0003t0004g0062others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1784+318A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294702 | ||||||
| chr11:18294760
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1784+260C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294760 | ||||||
| chr11:18294766
|
C | T | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1784+254G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294766 | ||||||
| chr11:18294831
|
T | TA | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1784+188dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294831 | ||||||
| chr11:18294873
|
T | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1784+147A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294873 | ||||||
| chr11:18294882
|
G | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1784+138C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294882 | ||||||
| chr11:18294955
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1784+65A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 14/22 | chr11 | 18294955 | ||||||
| chr11:18295173
|
G | C | 7 | a0001c0001t0001g0244a0001c0001t0002g0256a0001c0001t0002g0259others(4): Show | 7 | HG02132.hp2 HG02135.hp2 NA18992.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1635-4C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 13/22 | chr11 | 18295173 | ||||||
| chr11:18295331
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0309a0001c0001t0001g0310others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635-162G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 13/22 | chr11 | 18295331 | ||||||
| chr11:18295345
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1635-176G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 13/22 | chr11 | 18295345 | ||||||
| chr11:18295884
|
T | C | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1634+115A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 13/22 | chr11 | 18295884 | ||||||
| chr11:18295911
|
T | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(151): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1634+88A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 13/22 | chr11 | 18295911 | ||||||
| chr11:18296152
|
C | T | 238 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(235): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1511-30G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296152 | ||||||
| chr11:18296170
|
G | A | 5 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0300others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1511-48C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296170 | ||||||
| chr11:18296317
|
C | A | 126 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(123): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1511-195G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296317 | ||||||
| chr11:18296478
|
T | C | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1510+320A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296478 | ||||||
| chr11:18296600
|
G | A | 1 | a0013c0012t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1510+198C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296600 | ||||||
| chr11:18296681
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1510+117G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296681 | ||||||
| chr11:18296740
|
G | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1510+58C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 12/22 | chr11 | 18296740 | ||||||
| chr11:18297003
|
C | CA | 52 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(49): Show | 58 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1324-20dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 11/22 | chr11 | 18297003 | ||||||
| chr11:18297003
|
CA | C | 18 | a0001c0001t0002g0249a0001c0001t0005g0015a0001c0001t0005g0306others(15): Show | 21 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1324-20delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 11/22 | chr11 | 18297003 | ||||||
| chr11:18297047
|
A | G | 1 | a0002c0002t0002g0229 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1324-63T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 11/22 | chr11 | 18297047 | ||||||
| chr11:18297732
|
G | T | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1165-15C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18297732 | ||||||
| chr11:18297737
|
A | G | 6 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | HG00621.hp2 HG00642.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-20T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18297737 | ||||||
| chr11:18297804
|
G | A | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1165-87C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18297804 | ||||||
| chr11:18297863
|
C | T | 1 | a0002c0002t0001g0240 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1165-146G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18297863 | ||||||
| chr11:18297874
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1165-157C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18297874 | ||||||
| chr11:18297996
|
T | C | 1 | a0001c0001t0006g0348 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1165-279A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18297996 | ||||||
| chr11:18298012
|
A | G | 239 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(236): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1165-295T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298012 | ||||||
| chr11:18298041
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1165-324A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298041 | ||||||
| chr11:18298048
|
C | G | 1 | a0002c0002t0002g0217 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1165-331G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298048 | ||||||
| chr11:18298155
|
G | C | 1 | a0001c0003t0001g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1165-438C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298155 | ||||||
| chr11:18298156
|
C | T | 1 | a0001c0003t0001g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1165-439G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298156 | ||||||
| chr11:18298157
|
T | C | 1 | a0001c0003t0001g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1165-440A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298157 | ||||||
| chr11:18298184
|
G | T | 3 | a0001c0001t0003g0177a0001c0001t0003g0180a0001c0001t0004g0189 | 3 | HG00099.hp1 HG01109.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1165-467C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298184 | ||||||
| chr11:18298266
|
C | T | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+526G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298266 | ||||||
| chr11:18298281
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1164+511G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298281 | ||||||
| chr11:18298321
|
G | A | 11 | a0001c0001t0005g0015a0001c0001t0005g0306a0001c0001t0005g0307others(8): Show | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164+471C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298321 | ||||||
| chr11:18298368
|
G | A | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(237): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1164+424C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298368 | ||||||
| chr11:18298439
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1164+353C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298439 | ||||||
| chr11:18298476
|
C | T | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1164+316G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298476 | ||||||
| chr11:18298537
|
A | C | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1164+255T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298537 | ||||||
| chr11:18298605
|
G | T | 53 | a0002c0002t0001g0198a0002c0002t0001g0240a0002c0002t0002g0003others(50): Show | 59 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1164+187C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298605 | ||||||
| chr11:18298777
|
T | G | 1 | a0001c0001t0001g0338 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1164+15A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 10/22 | chr11 | 18298777 | ||||||
| chr11:18299010
|
A | C | 10 | a0001c0001t0013g0297a0001c0004t0001g0296a0001c0004t0001g0298others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.986-40T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299010 | ||||||
| chr11:18299066
|
C | T | 1 | a0001c0001t0006g0345 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.986-96G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299066 | ||||||
| chr11:18299098
|
A | G | 1 | a0001c0001t0003g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.986-128T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299098 | ||||||
| chr11:18299153
|
G | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.986-183C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299153 | ||||||
| chr11:18299172
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.986-202C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299172 | ||||||
| chr11:18299174
|
A | G | 3 | a0001c0001t0002g0246a0001c0001t0002g0247a0001c0001t0002g0248 | 3 | HG02074.hp1 NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.986-204T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299174 | ||||||
| chr11:18299213
|
A | T | 1 | a0001c0003t0001g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.986-243T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299213 | ||||||
| chr11:18299293
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.986-323C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299293 | ||||||
| chr11:18299458
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.986-488G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299458 | ||||||
| chr11:18299628
|
A | G | 1 | a0001c0001t0006g0348 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.986-658T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299628 | ||||||
| chr11:18299844
|
C | G | 1 | a0009c0013t0001g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.986-874G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18299844 | ||||||
| chr11:18300344
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.985+484A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300344 | ||||||
| chr11:18300396
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(133): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.985+432G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300396 | ||||||
| chr11:18300632
|
G | A | 4 | a0001c0001t0003g0093a0001c0001t0003g0094a0001c0001t0003g0166others(1): Show | 4 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.985+196C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300632 | ||||||
| chr11:18300688
|
C | A | 1 | a0001c0001t0003g0156 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.985+140G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300688 | ||||||
| chr11:18300696
|
CA | C | 11 | a0001c0003t0001g0027a0001c0003t0001g0032a0001c0003t0001g0036others(8): Show | 11 | HG01099.hp1 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.985+131delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300696 | ||||||
| chr11:18300696
|
CAAA | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0214others(60): Show | 72 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.985+129_985+131del others(3): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300696 | ||||||
| chr11:18300696
|
CAAAA | C | 77 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(74): Show | 82 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.985+128_985+131del others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300696 | ||||||
| chr11:18300696
|
CAAAAA | C | 142 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(139): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.985+127_985+131del others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 9/22 | chr11 | 18300696 | ||||||
| chr11:18300968
|
A | G | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.897-52T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18300968 | ||||||
| chr11:18300998
|
G | T | 60 | a0001c0001t0001g0207a0001c0001t0001g0244a0001c0001t0002g0012others(57): Show | 62 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.897-82C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18300998 | ||||||
| chr11:18301040
|
T | C | 3 | a0001c0001t0006g0017a0001c0001t0006g0347a0001c0001t0006g0348 | 4 | HG02922.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-124A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301040 | ||||||
| chr11:18301195
|
C | A | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.897-279G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301195 | ||||||
| chr11:18301316
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.897-400G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301316 | ||||||
| chr11:18301328
|
C | A | 2 | a0005c0007t0002g0223a0005c0007t0002g0227 | 2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.897-412G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301328 | ||||||
| chr11:18301360
|
G | A | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.897-444C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301360 | ||||||
| chr11:18301377
|
A | C | 292 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(289): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.897-461T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301377 | ||||||
| chr11:18301385
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0140 | 2 | NA18962.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.897-469C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301385 | ||||||
| chr11:18301454
|
C | CA | 33 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0001g0207others(30): Show | 35 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.897-539dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301454 | ||||||
| chr11:18301454
|
C | CAAAA | 50 | a0002c0002t0001g0198a0002c0002t0001g0240a0002c0002t0002g0003others(47): Show | 56 | HG00423.hp2 HG00621.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.897-542_897-539dup others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301454 | ||||||
| chr11:18301454
|
CA | C | 37 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0119others(34): Show | 39 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.897-539delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301454 | ||||||
| chr11:18301575
|
C | G | 1 | a0001c0003t0001g0046 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.897-659G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301575 | ||||||
| chr11:18301576
|
G | A | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.897-660C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301576 | ||||||
| chr11:18301676
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.897-760C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301676 | ||||||
| chr11:18301686
|
G | T | 1 | a0001c0001t0001g0313 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.897-770C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301686 | ||||||
| chr11:18301695
|
T | A | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.897-779A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301695 | ||||||
| chr11:18301696
|
C | A | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.897-780G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301696 | ||||||
| chr11:18301749
|
A | G | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.897-833T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301749 | ||||||
| chr11:18301769
|
G | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(133): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.897-853C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301769 | ||||||
| chr11:18301832
|
C | A | 1 | a0001c0003t0001g0046 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.897-916G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301832 | ||||||
| chr11:18301937
|
T | C | 1 | a0001c0001t0003g0154 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.897-1021A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301937 | ||||||
| chr11:18301970
|
T | C | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.897-1054A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18301970 | ||||||
| chr11:18302006
|
T | A | 2 | a0001c0001t0002g0175a0001c0001t0002g0276 | 2 | NA18951.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.897-1090A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302006 | ||||||
| chr11:18302126
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.897-1210G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302126 | ||||||
| chr11:18302222
|
A | G | 1 | a0001c0001t0010g0018 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.897-1306T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302222 | ||||||
| chr11:18302281
|
T | C | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.897-1365A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302281 | ||||||
| chr11:18302511
|
T | A | 1 | a0001c0003t0001g0020 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.897-1595A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302511 | ||||||
| chr11:18302514
|
T | A | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.897-1598A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302514 | ||||||
| chr11:18302550
|
T | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.897-1634A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302550 | ||||||
| chr11:18302670
|
C | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.897-1754G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302670 | ||||||
| chr11:18302742
|
T | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.897-1826A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302742 | ||||||
| chr11:18302791
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.897-1875C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302791 | ||||||
| chr11:18302816
|
A | G | 1 | a0001c0003t0004g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.897-1900T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302816 | ||||||
| chr11:18302822
|
C | CGG | 50 | a0001c0001t0001g0007a0001c0001t0001g0083a0001c0001t0001g0088others(47): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.897-1908_897-1907d others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302822 | ||||||
| chr11:18302822
|
C | CGGG | 36 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0101others(33): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.897-1909_897-1907d others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302822 | ||||||
| chr11:18302822
|
C | CGGGGGGG others(7): Show |
1 | a0001c0003t0001g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.897-1920_897-1907d others(16): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302822 | ||||||
| chr11:18302830
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0002g0255 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.897-1915_897-1914i others(12): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302830 | ||||||
| chr11:18302830
|
G | GGGGGGGG others(4): Show |
1 | a0001c0001t0002g0283 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.897-1915_897-1914i others(13): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302830 | ||||||
| chr11:18302830
|
G | GGGGGGGG others(6): Show |
2 | a0001c0001t0001g0328a0001c0001t0013g0297 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.897-1915_897-1914i others(15): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302830 | ||||||
| chr11:18302831
|
G | GGAGGGGG others(6): Show |
1 | a0001c0003t0001g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.897-1916_897-1915i others(15): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGAGGGG others(8): Show |
2 | a0001c0003t0001g0024a0001c0003t0001g0026 | 2 | HG01167.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.897-1916_897-1915i others(17): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGAGGGG others(9): Show |
1 | a0001c0003t0001g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.897-1916_897-1915i others(18): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGAGGG others(12): Show |
1 | a0001c0003t0001g0023 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.897-1916_897-1915i others(21): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGA | 34 | a0001c0001t0001g0137a0001c0001t0003g0112a0001c0004t0001g0296others(31): Show | 38 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(8): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGA | 25 | a0001c0001t0001g0076a0001c0004t0001g0301a0001c0004t0001g0305others(22): Show | 27 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(9): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(3): Show |
22 | a0001c0001t0001g0333a0001c0001t0002g0249a0001c0001t0002g0251others(19): Show | 22 | HG00597.hp2 HG00609.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(12): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(4): Show |
21 | a0001c0001t0001g0075a0001c0001t0001g0207a0001c0001t0002g0175others(18): Show | 21 | HG01934.hp2 HG01993.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(13): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(5): Show |
12 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0244others(9): Show | 14 | HG00735.hp1 HG02004.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(14): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(6): Show |
9 | a0001c0001t0001g0078a0001c0001t0002g0210a0001c0001t0002g0264others(6): Show | 9 | HG00280.hp2 HG00642.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(15): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(7): Show |
13 | a0001c0001t0002g0243a0001c0001t0002g0245a0001c0001t0002g0246others(10): Show | 13 | HG01074.hp2 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(16): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(8): Show |
5 | a0001c0001t0002g0279a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 5 | HG03492.hp2 NA18522.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(17): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(9): Show |
11 | a0001c0003t0001g0022a0001c0003t0001g0031a0001c0003t0001g0036others(8): Show | 11 | HG01169.hp1 HG01175.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(18): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(10): Show |
5 | a0001c0001t0001g0324a0001c0003t0001g0020a0001c0003t0004g0066others(2): Show | 5 | HG01243.hp1 HG01361.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(19): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(11): Show |
11 | a0001c0001t0002g0284a0001c0003t0001g0027a0001c0003t0001g0034others(8): Show | 11 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.897-1916_897-1915i others(20): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(12): Show |
1 | a0001c0003t0004g0064 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.897-1916_897-1915i others(21): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(13): Show |
1 | a0001c0003t0003g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.897-1916_897-1915i others(22): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(14): Show |
2 | a0001c0003t0004g0061a0001c0003t0004g0062 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.897-1916_897-1915i others(23): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302831
|
G | GGGGGGGG others(17): Show |
1 | a0001c0003t0001g0035 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.897-1916_897-1915i others(26): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302831 | ||||||
| chr11:18302845
|
G | C | 1 | a0001c0001t0003g0186 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.897-1929C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302845 | ||||||
| chr11:18302849
|
C | T | 66 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105others(63): Show | 68 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.897-1933G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302849 | ||||||
| chr11:18302939
|
G | A | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.897-2023C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302939 | ||||||
| chr11:18302952
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.897-2036C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18302952 | ||||||
| chr11:18303048
|
G | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.897-2132C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303048 | ||||||
| chr11:18303068
|
G | GAAAGTGA others(4): Show |
54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.897-2153_897-2152i others(13): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303068 | ||||||
| chr11:18303185
|
T | C | 1 | a0001c0001t0003g0138 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.896+2237A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303185 | ||||||
| chr11:18303276
|
T | TA | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.896+2145_896+2146i others(3): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303276 | ||||||
| chr11:18303290
|
C | A | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+2132G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303290 | ||||||
| chr11:18303453
|
C | T | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.896+1969G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303453 | ||||||
| chr11:18303464
|
GCAGAGCC others(14): Show |
G | 1 | a0001c0001t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.896+1937_896+1957d others(23): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303464 | ||||||
| chr11:18303485
|
CT | C | 4 | a0001c0003t0004g0028a0001c0003t0009g0342a0001c0003t0009g0343others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+1936delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303485 | ||||||
| chr11:18303511
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0002g0231 | 3 | HG01891.hp1 HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.896+1911A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303511 | ||||||
| chr11:18303599
|
C | T | 132 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(129): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.896+1823G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303599 | ||||||
| chr11:18303618
|
C | T | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.896+1804G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303618 | ||||||
| chr11:18303721
|
C | T | 60 | a0001c0001t0001g0207a0001c0001t0001g0244a0001c0001t0002g0012others(57): Show | 62 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.896+1701G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303721 | ||||||
| chr11:18303726
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+1696C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303726 | ||||||
| chr11:18303753
|
C | A | 10 | a0001c0003t0004g0029a0001c0003t0004g0030a0001c0003t0004g0059others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.896+1669G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303753 | ||||||
| chr11:18303792
|
T | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.896+1630A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303792 | ||||||
| chr11:18303854
|
T | TA | 69 | a0001c0001t0001g0074a0001c0001t0001g0104a0001c0001t0001g0140others(66): Show | 75 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.896+1567dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303854 | ||||||
| chr11:18303854
|
TA | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(12): Show | 18 | HG01168.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.896+1567delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303854 | ||||||
| chr11:18303921
|
A | C | 1 | a0002c0002t0002g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.896+1501T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303921 | ||||||
| chr11:18303946
|
G | T | 1 | a0001c0001t0002g0256 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.896+1476C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303946 | ||||||
| chr11:18303968
|
G | GA | 10 | a0001c0001t0013g0297a0001c0004t0001g0296a0001c0004t0001g0298others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.896+1453dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18303968 | ||||||
| chr11:18304006
|
A | G | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.896+1416T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304006 | ||||||
| chr11:18304119
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+1303C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304119 | ||||||
| chr11:18304216
|
C | CT | 21 | a0001c0001t0001g0075a0001c0001t0001g0244a0001c0001t0002g0245others(18): Show | 21 | HG01169.hp1 HG01261.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+1205dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304216 | ||||||
| chr11:18304269
|
T | G | 80 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0074others(77): Show | 85 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.896+1153A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304269 | ||||||
| chr11:18304274
|
T | C | 1 | a0001c0001t0010g0018 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.896+1148A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304274 | ||||||
| chr11:18304320
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.896+1102C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304320 | ||||||
| chr11:18304509
|
G | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.896+913C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304509 | ||||||
| chr11:18304649
|
C | G | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.896+773G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304649 | ||||||
| chr11:18304809
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.896+613G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304809 | ||||||
| chr11:18304995
|
T | C | 147 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(144): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.896+427A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18304995 | ||||||
| chr11:18305162
|
G | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.896+260C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305162 | ||||||
| chr11:18305165
|
G | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.896+257C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305165 | ||||||
| chr11:18305168
|
C | A | 61 | a0001c0001t0001g0207a0001c0001t0001g0244a0001c0001t0002g0012others(58): Show | 63 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.896+254G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305168 | ||||||
| chr11:18305174
|
T | A | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+248A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305174 | ||||||
| chr11:18305211
|
C | T | 238 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(235): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.896+211G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305211 | ||||||
| chr11:18305278
|
C | T | 10 | a0001c0001t0013g0297a0001c0004t0001g0296a0001c0004t0001g0298others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.896+144G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305278 | ||||||
| chr11:18305359
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.896+63T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305359 | ||||||
| chr11:18305370
|
A | C | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.896+52T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 8/22 | chr11 | 18305370 | ||||||
| chr11:18305575
|
T | G | 11 | a0001c0001t0005g0015a0001c0001t0005g0306a0001c0001t0005g0307others(8): Show | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.825-82A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305575 | ||||||
| chr11:18305664
|
C | G | 3 | a0002c0002t0002g0221a0002c0002t0002g0236a0002c0002t0002g0237 | 3 | HG01256.hp2 HG01258.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.825-171G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305664 | ||||||
| chr11:18305701
|
C | T | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.825-208G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305701 | ||||||
| chr11:18305710
|
C | T | 1 | a0001c0003t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.825-217G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305710 | ||||||
| chr11:18305721
|
T | C | 1 | a0001c0001t0003g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.825-228A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305721 | ||||||
| chr11:18305732
|
C | CT | 8 | a0001c0003t0001g0033a0001c0003t0004g0029a0001c0003t0004g0069others(5): Show | 8 | HG00741.hp1 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.825-240dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305732 | ||||||
| chr11:18305732
|
CT | C | 225 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(222): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.825-240delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305732 | ||||||
| chr11:18305772
|
A | G | 292 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(289): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.825-279T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305772 | ||||||
| chr11:18305777
|
C | G | 311 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(308): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.825-284G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305777 | ||||||
| chr11:18305779
|
C | T | 1 | a0008c0023t0002g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.825-286G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305779 | ||||||
| chr11:18305798
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.825-305A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305798 | ||||||
| chr11:18305801
|
T | C | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.825-308A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305801 | ||||||
| chr11:18305803
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.825-310C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305803 | ||||||
| chr11:18305839
|
C | T | 2 | a0002c0002t0002g0217a0002c0002t0002g0239 | 2 | NA18612.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.824+296G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305839 | ||||||
| chr11:18305878
|
C | T | 53 | a0002c0002t0001g0198a0002c0002t0001g0240a0002c0002t0002g0003others(50): Show | 59 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.824+257G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305878 | ||||||
| chr11:18305929
|
T | TCACCC | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.824+205_824+206ins others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305929 | ||||||
| chr11:18305936
|
G | A | 11 | a0001c0001t0005g0015a0001c0001t0005g0306a0001c0001t0005g0307others(8): Show | 13 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.824+199C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305936 | ||||||
| chr11:18305952
|
T | A | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.824+183A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305952 | ||||||
| chr11:18305958
|
TCCTGACC others(14): Show |
T | 1 | a0001c0001t0002g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.824+156_824+176del others(21): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305958 | ||||||
| chr11:18305974
|
C | T | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.824+161G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18305974 | ||||||
| chr11:18306101
|
T | G | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.824+34A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 7/22 | chr11 | 18306101 | ||||||
| chr11:18306642
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.612-295C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18306642 | ||||||
| chr11:18306879
|
A | G | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.612-532T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18306879 | ||||||
| chr11:18306915
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.612-568C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18306915 | ||||||
| chr11:18306981
|
CATCATTC others(14): Show |
C | 60 | a0001c0001t0001g0207a0001c0001t0001g0244a0001c0001t0002g0012others(57): Show | 62 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.612-655_612-635del others(21): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18306981 | ||||||
| chr11:18307052
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.612-705C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307052 | ||||||
| chr11:18307123
|
C | T | 1 | a0001c0001t0011g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.612-776G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307123 | ||||||
| chr11:18307127
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.612-780T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307127 | ||||||
| chr11:18307195
|
G | T | 1 | a0001c0001t0002g0293 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.612-848C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307195 | ||||||
| chr11:18307459
|
T | C | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.612-1112A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307459 | ||||||
| chr11:18307518
|
ACAT | A | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.612-1174_612-1172d others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307518 | ||||||
| chr11:18307673
|
T | A | 1 | a0002c0002t0002g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.611+1273A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307673 | ||||||
| chr11:18307690
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.611+1256T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307690 | ||||||
| chr11:18307747
|
A | C | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.611+1199T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307747 | ||||||
| chr11:18307761
|
A | C | 1 | a0006c0006t0002g0254 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.611+1185T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307761 | ||||||
| chr11:18307792
|
G | A | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG01952.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.611+1154C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307792 | ||||||
| chr11:18307813
|
A | C | 4 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0317others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.611+1133T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18307813 | ||||||
| chr11:18308004
|
T | C | 3 | a0001c0001t0003g0142a0001c0001t0003g0143a0001c0001t0003g0144 | 3 | HG00140.hp1 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.611+942A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18308004 | ||||||
| chr11:18308051
|
C | A | 3 | a0001c0001t0008g0011a0001c0001t0008g0095a0001c0001t0008g0185 | 4 | HG00735.hp2 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+895G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18308051 | ||||||
| chr11:18308248
|
T | A | 1 | a0001c0001t0003g0180 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.611+698A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18308248 | ||||||
| chr11:18308800
|
AG | A | 5 | a0001c0001t0002g0245a0001c0001t0002g0253a0001c0001t0002g0267others(2): Show | 5 | NA18965.hp1 NA18972.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+145delC | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18308800 | ||||||
| chr11:18308838
|
G | GA | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.611+107dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 6/22 | chr11 | 18308838 | ||||||
| chr11:18309186
|
A | C | 1 | a0004c0005t0003g0111 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.478-107T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309186 | ||||||
| chr11:18309429
|
G | C | 9 | a0001c0001t0001g0087a0001c0001t0003g0080a0001c0001t0003g0081others(6): Show | 9 | HG00558.hp1 HG01952.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-350C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309429 | ||||||
| chr11:18309467
|
G | A | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-388C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309467 | ||||||
| chr11:18309724
|
G | A | 2 | a0001c0001t0003g0315a0001c0001t0003g0318 | 2 | HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.478-645C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309724 | ||||||
| chr11:18309829
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.478-750A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309829 | ||||||
| chr11:18309935
|
C | T | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.477+806G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309935 | ||||||
| chr11:18309942
|
G | T | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.477+799C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309942 | ||||||
| chr11:18309944
|
A | C | 1 | a0001c0001t0002g0175 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.477+797T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309944 | ||||||
| chr11:18309952
|
A | T | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.477+789T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309952 | ||||||
| chr11:18309956
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.477+785A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309956 | ||||||
| chr11:18309996
|
C | G | 1 | a0002c0024t0002g0219 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.477+745G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18309996 | ||||||
| chr11:18310016
|
A | G | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.477+725T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18310016 | ||||||
| chr11:18310081
|
A | G | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.477+660T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18310081 | ||||||
| chr11:18310118
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+623C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18310118 | ||||||
| chr11:18310210
|
C | T | 1 | a0003c0019t0003g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.477+531G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18310210 | ||||||
| chr11:18310428
|
ATATCT | A | 3 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0003g0336 | 3 | HG00642.hp2 HG01175.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.477+308_477+312del others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18310428 | ||||||
| chr11:18310480
|
T | C | 1 | a0001c0004t0001g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.477+261A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 5/22 | chr11 | 18310480 | ||||||
| chr11:18310943
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.285-10A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 4/22 | chr11 | 18310943 | ||||||
| chr11:18311177
|
C | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.284+210G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 4/22 | chr11 | 18311177 | ||||||
| chr11:18311360
|
A | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.284+27T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 4/22 | chr11 | 18311360 | ||||||
| chr11:18311495
|
C | CATT | 67 | a0001c0001t0001g0007a0001c0001t0001g0090a0001c0001t0001g0091others(64): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.220-47_220-45dupAA others(1): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311495 | ||||||
| chr11:18311508
|
A | AT | 6 | a0001c0001t0005g0306a0001c0001t0005g0320a0001c0001t0005g0321others(3): Show | 7 | HG00735.hp2 HG01070.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-58dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311508 | ||||||
| chr11:18311508
|
A | ATT | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0013c0012t0002g0213 | 3 | HG02809.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.220-59_220-58dupAA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311508 | ||||||
| chr11:18311508
|
A | ATTT | 4 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0174others(1): Show | 4 | NA19000.hp2 NA19010.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-58_220-57insAA others(1): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311508 | ||||||
| chr11:18311511
|
A | AT | 12 | a0001c0001t0005g0307a0001c0001t0005g0308a0001c0001t0005g0322others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-61dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311511 | ||||||
| chr11:18311511
|
A | ATT | 14 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0312others(11): Show | 14 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-62_220-61dupAA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311511 | ||||||
| chr11:18311511
|
A | ATTT | 102 | a0001c0001t0001g0014a0001c0001t0001g0082a0001c0001t0001g0083others(99): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.220-63_220-61dupAA others(1): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311511 | ||||||
| chr11:18311511
|
A | T | 20 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0330others(17): Show | 21 | HG00735.hp2 HG01070.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-60T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311511 | ||||||
| chr11:18311512
|
T | TTA | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 13 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.220-62_220-61insTA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311512 | ||||||
| chr11:18311513
|
T | TA | 11 | a0001c0001t0005g0323a0001c0001t0013g0297a0001c0003t0004g0059others(8): Show | 11 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-63_220-62insT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311513 | ||||||
| chr11:18311514
|
T | A | 92 | a0001c0001t0001g0092a0001c0001t0001g0324a0001c0001t0001g0325others(89): Show | 98 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.220-63A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311514 | ||||||
| chr11:18311515
|
T | A | 1 | a0002c0002t0002g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.220-64A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311515 | ||||||
| chr11:18311517
|
T | A | 2 | a0001c0003t0001g0047a0002c0002t0002g0058 | 2 | HG02647.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.220-66A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311517 | ||||||
| chr11:18311700
|
G | A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.219+214C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311700 | ||||||
| chr11:18311733
|
A | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+181T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311733 | ||||||
| chr11:18311889
|
A | T | 59 | a0001c0001t0001g0207a0001c0001t0001g0244a0001c0001t0002g0012others(56): Show | 61 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.219+25T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 3/22 | chr11 | 18311889 | ||||||
| chr11:18312095
|
A | C | 1 | a0001c0001t0003g0107 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109-71T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18312095 | ||||||
| chr11:18312329
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.109-305C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18312329 | ||||||
| chr11:18312487
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.109-463G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18312487 | ||||||
| chr11:18312672
|
G | A | 3 | a0001c0001t0008g0011a0001c0001t0008g0095a0001c0001t0008g0185 | 4 | HG00735.hp2 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-648C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18312672 | ||||||
| chr11:18312687
|
G | C | 1 | a0001c0001t0002g0267 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.109-663C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18312687 | ||||||
| chr11:18312797
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.109-773T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18312797 | ||||||
| chr11:18313103
|
G | A | 2 | a0001c0003t0001g0027a0001c0003t0001g0047 | 2 | NA19070.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.109-1079C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313103 | ||||||
| chr11:18313222
|
GA | G | 10 | a0001c0001t0013g0297a0001c0004t0001g0296a0001c0004t0001g0298others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-1199delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313222 | ||||||
| chr11:18313566
|
G | T | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109-1542C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313566 | ||||||
| chr11:18313587
|
A | AT | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-1564dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313587 | ||||||
| chr11:18313642
|
G | A | 79 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(76): Show | 83 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.109-1618C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313642 | ||||||
| chr11:18313653
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | NA18959.hp2 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.109-1629G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313653 | ||||||
| chr11:18313690
|
C | T | 1 | a0011c0021t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.109-1666G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313690 | ||||||
| chr11:18313691
|
G | A | 4 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(1): Show | 4 | NA18975.hp1 NA18985.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-1667C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313691 | ||||||
| chr11:18313810
|
A | T | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.109-1786T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313810 | ||||||
| chr11:18313843
|
A | G | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.109-1819T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313843 | ||||||
| chr11:18313908
|
G | A | 1 | a0002c0002t0002g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.109-1884C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313908 | ||||||
| chr11:18313912
|
C | CAA | 128 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(125): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.109-1890_109-1889d others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313912 | ||||||
| chr11:18313912
|
C | CAAA | 7 | a0001c0001t0001g0014a0001c0001t0001g0309a0001c0001t0001g0310others(4): Show | 8 | HG02895.hp1 HG02896.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-1891_109-1889d others(5): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313912 | ||||||
| chr11:18313912
|
CA | C | 68 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(65): Show | 70 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.109-1889delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313912 | ||||||
| chr11:18313924
|
A | G | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109-1900T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18313924 | ||||||
| chr11:18314137
|
G | A | 239 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(236): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.109-2113C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314137 | ||||||
| chr11:18314213
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.109-2189G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314213 | ||||||
| chr11:18314230
|
G | C | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109-2206C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314230 | ||||||
| chr11:18314243
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.109-2219G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314243 | ||||||
| chr11:18314323
|
G | A | 1 | a0014c0016t0003g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109-2299C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314323 | ||||||
| chr11:18314358
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(135): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.109-2334C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314358 | ||||||
| chr11:18314407
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18961.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.109-2383A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314407 | ||||||
| chr11:18314436
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.109-2412A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314436 | ||||||
| chr11:18314453
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.109-2429G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314453 | ||||||
| chr11:18314476
|
C | T | 1 | a0001c0001t0005g0322 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109-2452G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314476 | ||||||
| chr11:18314530
|
A | AAAAT | 7 | a0001c0001t0001g0207a0001c0001t0002g0210a0001c0001t0002g0293others(4): Show | 7 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-2510_109-2507d others(6): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314530 | ||||||
| chr11:18314530
|
A | AAAATAAA others(1): Show |
50 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(47): Show | 52 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.109-2514_109-2507d others(10): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314530 | ||||||
| chr11:18314530
|
A | AAAATAAA others(5): Show |
6 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247others(3): Show | 6 | HG02074.hp1 HG02602.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-2518_109-2507d others(14): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314530 | ||||||
| chr11:18314530
|
AAAATAAA others(1): Show |
A | 54 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(51): Show | 60 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.109-2514_109-2507d others(10): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314530 | ||||||
| chr11:18314677
|
C | T | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-2653G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314677 | ||||||
| chr11:18314858
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.109-2834C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314858 | ||||||
| chr11:18314912
|
G | A | 1 | a0002c0002t0002g0204 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108+2839C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314912 | ||||||
| chr11:18314925
|
C | T | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.108+2826G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314925 | ||||||
| chr11:18314999
|
CAGCTTCT others(7): Show |
C | 1 | a0001c0001t0003g0165 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.108+2738_108+2751d others(16): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18314999 | ||||||
| chr11:18315154
|
T | C | 1 | a0002c0002t0002g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.108+2597A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315154 | ||||||
| chr11:18315188
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.108+2563G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315188 | ||||||
| chr11:18315260
|
C | T | 1 | a0002c0002t0002g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.108+2491G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315260 | ||||||
| chr11:18315490
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.108+2261C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315490 | ||||||
| chr11:18315612
|
T | TA | 6 | a0001c0001t0001g0214a0001c0001t0005g0306a0001c0001t0005g0320others(3): Show | 6 | HG01070.hp2 HG01433.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+2138dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315612 | ||||||
| chr11:18315726
|
C | A | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.108+2025G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315726 | ||||||
| chr11:18315757
|
T | TA | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+1993dupT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315757 | ||||||
| chr11:18315929
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.108+1822A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18315929 | ||||||
| chr11:18316072
|
T | C | 1 | a0003c0019t0003g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.108+1679A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316072 | ||||||
| chr11:18316086
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+1665T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316086 | ||||||
| chr11:18316374
|
T | C | 1 | a0015c0015t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.108+1377A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316374 | ||||||
| chr11:18316503
|
G | A | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+1248C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316503 | ||||||
| chr11:18316511
|
G | A | 1 | a0013c0012t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108+1240C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316511 | ||||||
| chr11:18316655
|
T | C | 64 | a0001c0001t0001g0214a0001c0001t0005g0015a0001c0001t0005g0306others(61): Show | 72 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.108+1096A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316655 | ||||||
| chr11:18316861
|
G | A | 2 | a0001c0001t0001g0317a0001c0001t0001g0319 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.108+890C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316861 | ||||||
| chr11:18316865
|
G | A | 1 | a0001c0001t0013g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.108+886C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316865 | ||||||
| chr11:18316960
|
C | T | 1 | a0001c0003t0004g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.108+791G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18316960 | ||||||
| chr11:18317070
|
T | G | 1 | a0003c0019t0003g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.108+681A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317070 | ||||||
| chr11:18317088
|
G | A | 3 | a0001c0001t0003g0093a0001c0001t0003g0094a0001c0001t0003g0166 | 3 | HG01109.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.108+663C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317088 | ||||||
| chr11:18317127
|
G | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | NA18982.hp1 NA19074.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.108+624C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317127 | ||||||
| chr11:18317135
|
A | C | 138 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(135): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.108+616T>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317135 | ||||||
| chr11:18317189
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(135): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.108+562C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317189 | ||||||
| chr11:18317193
|
CA | C | 340 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(337): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.108+557delT | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317193 | ||||||
| chr11:18317257
|
A | AT | 25 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(22): Show | 31 | HG01106.hp1 HG01243.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.108+493dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317257 | ||||||
| chr11:18317257
|
AT | A | 136 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(133): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+493delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317257 | ||||||
| chr11:18317351
|
G | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(9): Show | 15 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.108+400C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317351 | ||||||
| chr11:18317380
|
C | T | 1 | a0001c0018t0002g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.108+371G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317380 | ||||||
| chr11:18317401
|
G | A | 9 | a0001c0004t0001g0296a0001c0004t0001g0298a0001c0004t0001g0299others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+350C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317401 | ||||||
| chr11:18317416
|
C | T | 1 | a0001c0001t0003g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.108+335G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317416 | ||||||
| chr11:18317417
|
G | A | 1 | a0001c0001t0007g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.108+334C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317417 | ||||||
| chr11:18317709
|
A | G | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+42T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 2/22 | chr11 | 18317709 | ||||||
| chr11:18317960
|
T | C | 1 | a0010c0020t0006g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-49-53A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18317960 | ||||||
| chr11:18318694
|
T | G | 64 | a0001c0001t0001g0214a0001c0001t0005g0015a0001c0001t0005g0306others(61): Show | 72 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-49-787A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18318694 | ||||||
| chr11:18318731
|
G | A | 1 | a0001c0003t0003g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49-824C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18318731 | ||||||
| chr11:18318943
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-1036G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18318943 | ||||||
| chr11:18318953
|
A | AT | 53 | a0001c0001t0001g0214a0002c0002t0001g0198a0002c0002t0001g0240others(50): Show | 59 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.-49-1047dupA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18318953 | ||||||
| chr11:18318970
|
C | T | 15 | a0002c0002t0001g0198a0002c0002t0002g0003a0002c0002t0002g0004others(12): Show | 19 | HG00621.hp1 HG02080.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-1063G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18318970 | ||||||
| chr11:18319207
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-49-1300T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319207 | ||||||
| chr11:18319223
|
G | C | 1 | a0001c0001t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-49-1316C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319223 | ||||||
| chr11:18319255
|
C | CCA | 19 | a0001c0001t0001g0079a0001c0001t0001g0319a0001c0001t0002g0210others(16): Show | 19 | HG01074.hp1 HG02074.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-1350_-49-1349d others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
C | CCACA | 23 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0002g0013others(20): Show | 25 | HG00609.hp1 HG01884.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.-49-1352_-49-1349d others(6): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
C | CCACACA | 49 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0214others(46): Show | 58 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-1354_-49-1349d others(8): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
C | CCACACAC others(1): Show |
17 | a0001c0001t0001g0330a0001c0001t0005g0307a0001c0001t0005g0308others(14): Show | 17 | HG02083.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-49-1356_-49-1349d others(10): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
C | CCACACAC others(3): Show |
6 | a0001c0001t0001g0331a0001c0001t0005g0015a0001c0001t0005g0322others(3): Show | 7 | HG00621.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-1358_-49-1349d others(12): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
C | CCACACAC others(5): Show |
1 | a0002c0002t0002g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-1360_-49-1349d others(14): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
CCA | C | 127 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(124): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-49-1350_-49-1349d others(4): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
CCACA | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(13): Show | 17 | HG01167.hp1 HG01169.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.-49-1352_-49-1349d others(6): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319255
|
CCACACA | C | 9 | a0001c0001t0001g0324a0001c0001t0003g0080a0001c0001t0003g0081others(6): Show | 9 | HG00323.hp1 HG00558.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-1354_-49-1349d others(8): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319255 | ||||||
| chr11:18319266
|
C | A | 1 | a0001c0001t0001g0339 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-49-1359G>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319266 | ||||||
| chr11:18319311
|
AT | A | 251 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0075others(248): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-49-1405delA | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319311 | ||||||
| chr11:18319315
|
G | A | 251 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0075others(248): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-49-1408C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319315 | ||||||
| chr11:18319348
|
G | A | 5 | a0001c0001t0006g0017a0001c0001t0006g0345a0001c0001t0006g0347others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-1441C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319348 | ||||||
| chr11:18319647
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0309a0001c0001t0001g0310others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-1740C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319647 | ||||||
| chr11:18319655
|
T | C | 56 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(53): Show | 58 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-49-1748A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319655 | ||||||
| chr11:18319663
|
T | C | 1 | a0002c0002t0002g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-1756A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319663 | ||||||
| chr11:18319692
|
T | C | 1 | a0001c0001t0004g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-49-1785A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319692 | ||||||
| chr11:18319788
|
A | T | 15 | a0002c0002t0001g0198a0002c0002t0002g0003a0002c0002t0002g0004others(12): Show | 19 | HG00621.hp1 HG02080.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-1881T>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319788 | ||||||
| chr11:18319883
|
G | A | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-49-1976C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319883 | ||||||
| chr11:18319956
|
T | C | 7 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0316others(4): Show | 7 | HG02451.hp2 HG02738.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+1990A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18319956 | ||||||
| chr11:18320039
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-50+1907C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320039 | ||||||
| chr11:18320045
|
G | A | 7 | a0001c0003t0004g0060a0001c0003t0004g0061a0001c0003t0004g0062others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+1901C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320045 | ||||||
| chr11:18320062
|
C | T | 3 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0014t0001g0334 | 3 | HG02622.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-50+1884G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320062 | ||||||
| chr11:18320066
|
G | A | 5 | a0001c0003t0004g0068a0001c0003t0004g0069a0001c0003t0004g0070others(2): Show | 5 | HG01074.hp2 HG01175.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+1880C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320066 | ||||||
| chr11:18320070
|
T | G | 6 | a0001c0001t0005g0015a0001c0001t0005g0320a0001c0001t0005g0321others(3): Show | 7 | HG01070.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+1876A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320070 | ||||||
| chr11:18320093
|
T | C | 1 | a0001c0001t0003g0190 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-50+1853A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320093 | ||||||
| chr11:18320305
|
T | C | 3 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0014t0001g0334 | 3 | HG02622.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-50+1641A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320305 | ||||||
| chr11:18320322
|
A | G | 125 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(122): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.-50+1624T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320322 | ||||||
| chr11:18320402
|
TTCAGCCA others(7): Show |
T | 1 | a0001c0003t0001g0020 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-50+1530_-50+1543d others(16): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320402 | ||||||
| chr11:18320534
|
T | C | 237 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(234): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-50+1412A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320534 | ||||||
| chr11:18320613
|
G | T | 243 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0075others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.-50+1333C>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320613 | ||||||
| chr11:18320658
|
C | G | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-50+1288G>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320658 | ||||||
| chr11:18320739
|
G | A | 1 | a0002c0002t0014g0341 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-50+1207C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320739 | ||||||
| chr11:18320777
|
T | G | 1 | a0001c0003t0003g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-50+1169A>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320777 | ||||||
| chr11:18320831
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-50+1115G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320831 | ||||||
| chr11:18320832
|
T | A | 1 | a0001c0001t0001g0339 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-50+1114A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320832 | ||||||
| chr11:18320847
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0324others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+1099A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320847 | ||||||
| chr11:18320960
|
G | C | 1 | a0001c0001t0007g0335 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-50+986C>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18320960 | ||||||
| chr11:18321091
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-50+855T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321091 | ||||||
| chr11:18321151
|
TAAA | T | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+792_-50+794del others(3): Show |
HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321151 | ||||||
| chr11:18321171
|
T | C | 3 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0003g0336 | 3 | HG00642.hp2 HG01175.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-50+775A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321171 | ||||||
| chr11:18321207
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-50+739G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321207 | ||||||
| chr11:18321208
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-50+738A>G | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321208 | ||||||
| chr11:18321213
|
T | A | 1 | a0004c0005t0003g0340 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-50+733A>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321213 | ||||||
| chr11:18321370
|
A | G | 2 | a0001c0001t0006g0345a0010c0020t0006g0346 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-50+576T>C | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321370 | ||||||
| chr11:18321662
|
G | A | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(288): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-50+284C>T | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321662 | ||||||
| chr11:18321835
|
C | T | 1 | a0002c0002t0003g0019 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-50+111G>A | HPS5 | ENSG00000110756.18 | transcript | ENST00000349215.8 | protein_coding | 1/22 | chr11 | 18321835 |