Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84343 |
| ensemblid | ENSG00000163755.9 |
| hgncid | 15597 |
| symbol | HPS3 |
| name | HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 |
| refseq_nuc | NM_032383.5 |
| refseq_prot | NP_115759.2 |
| ensembl_nuc | ENST00000296051.7 |
| ensembl_prot | ENSP00000296051.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 149129638 |
| end | 149173732 |
| strand | + |
| ver | v1.2 |
| region | chr3:149129638-149173732 |
| region5000 | chr3:149124638-149178732 |
| regionname0 | HPS3_chr3_149129638_149173732 |
| regionname5000 | HPS3_chr3_149124638_149178732 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1004 | 373 | 86 | 57 | 162 | 18 | 48 | 124 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0002 | 0/0 | 1004 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0003 | 0/0 | 1004 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0004 | 0/0 | 1004 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0005 | 0/0 | 1004 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0006 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0007 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0008 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0009 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0010 | 0/0 | 1004 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| a0011 | 0/0 | 1004 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | MVQLY others(999): Show |
chr3 | 149124638 | 149178732 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3012 | 112 | 7 | 19 | 64 | 6 | 15 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0002 | 0/0 | 3012 | 85 | 36 | 12 | 22 | 3 | 12 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0003 | 0/0 | 3012 | 72 | 22 | 11 | 26 | 7 | 6 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0004 | 0/1 | 3012 | 62 | 1 | 8 | 43 | 2 | 7 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0005 | 0/0 | 3012 | 25 | 19 | 5 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0006 | 0/0 | 3012 | 5 | 0 | 1 | 0 | 0 | 4 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0011 | 0/0 | 3012 | 2 | 0 | 0 | 0 | 0 | 2 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0012 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0013 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0014 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0015 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0018 | 0/0 | 3012 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0019 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0021 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0022 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0023 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0001c0024 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0002c0007 | 0/0 | 3012 | 4 | 4 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0003c0008 | 0/0 | 3012 | 3 | 3 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0004c0009 | 0/0 | 3012 | 3 | 0 | 0 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0005c0010 | 0/0 | 3012 | 3 | 0 | 0 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0006c0020 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0007c0017 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0008c0026 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0009c0027 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0010c0016 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 | ||
| a0011c0025 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | ATGGT others(3007): Show |
chr3 | 149124638 | 149178732 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4611 | 74 | 3 | 13 | 43 | 5 | 9 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0002 | 0/0 | 4615 | 5 | 0 | 0 | 4 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0003 | 0/0 | 4611 | 4 | 1 | 0 | 2 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0004 | 0/0 | 4613 | 9 | 3 | 2 | 4 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0005 | 0/0 | 4617 | 9 | 0 | 3 | 5 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4612): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0006 | 0/0 | 4619 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0007 | 0/0 | 4609 | 4 | 0 | 0 | 4 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4604): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0008 | 0/0 | 4619 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0011 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4604): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0021 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0038 | 0/0 | 4611 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0041 | 0/0 | 4623 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4618): Show |
chr3 | 149124638 | 149178732 |
| a0001c0001t0042 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0001 | 0/0 | 4611 | 5 | 3 | 0 | 1 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0002 | 0/0 | 4615 | 3 | 0 | 1 | 1 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0003 | 0/0 | 4611 | 31 | 12 | 1 | 18 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0004 | 0/0 | 4613 | 2 | 1 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0006 | 0/0 | 4619 | 7 | 7 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0008 | 0/0 | 4619 | 10 | 0 | 4 | 0 | 0 | 6 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0009 | 0/0 | 4611 | 4 | 0 | 1 | 1 | 1 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0010 | 0/0 | 4620 | 4 | 3 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4615): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0011 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4604): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0012 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4619): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0013 | 0/0 | 4612 | 3 | 3 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4607): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0016 | 0/0 | 4613 | 3 | 0 | 2 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0017 | 0/0 | 4621 | 3 | 0 | 0 | 0 | 0 | 3 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4616): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0021 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0027 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0029 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4622): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0030 | 0/0 | 4625 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4620): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0032 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4616): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0034 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4617): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0035 | 0/0 | 4616 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4611): Show |
chr3 | 149124638 | 149178732 |
| a0001c0002t0037 | 0/0 | 4611 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0001 | 0/0 | 4611 | 38 | 6 | 9 | 16 | 3 | 4 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0002 | 0/0 | 4615 | 5 | 3 | 0 | 0 | 2 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0003 | 0/0 | 4611 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0004 | 0/0 | 4613 | 7 | 3 | 0 | 3 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0005 | 0/0 | 4617 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4612): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0007 | 0/0 | 4609 | 8 | 7 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4604): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0009 | 0/0 | 4611 | 5 | 0 | 1 | 4 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0015 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4607): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0018 | 0/0 | 4611 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0020 | 0/0 | 4613 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0003t0022 | 0/0 | 4611 | 2 | 0 | 0 | 0 | 2 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0001 | 0/0 | 4611 | 7 | 0 | 1 | 6 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0002 | 0/1 | 4615 | 40 | 0 | 6 | 28 | 1 | 4 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0004 | 0/0 | 4613 | 8 | 0 | 1 | 5 | 1 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4608): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0005 | 0/0 | 4617 | 4 | 0 | 0 | 3 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4612): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0006 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0008 | 0/0 | 4619 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0004t0025 | 0/0 | 4615 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0001 | 0/0 | 4611 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0003 | 0/0 | 4611 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0005 | 0/0 | 4617 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4612): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0006 | 0/0 | 4619 | 3 | 2 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4614): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0010 | 0/0 | 4620 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4615): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0012 | 0/0 | 4624 | 3 | 2 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4619): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0014 | 0/0 | 4626 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4621): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0015 | 0/0 | 4612 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4607): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0018 | 0/0 | 4611 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0019 | 0/0 | 4618 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4613): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0023 | 0/0 | 4625 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4620): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0026 | 0/0 | 4627 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4622): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0028 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4627): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0031 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4621): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0033 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4616): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0036 | 0/0 | 4614 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4609): Show |
chr3 | 149124638 | 149178732 |
| a0001c0005t0040 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4589): Show |
chr3 | 149124638 | 149178732 |
| a0001c0006t0001 | 0/0 | 4611 | 2 | 0 | 1 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0006t0011 | 0/0 | 4609 | 3 | 0 | 0 | 0 | 0 | 3 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4604): Show |
chr3 | 149124638 | 149178732 |
| a0001c0011t0001 | 0/0 | 4611 | 2 | 0 | 0 | 0 | 0 | 2 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0012t0002 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0013t0001 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0014t0009 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0015t0001 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0018t0001 | 0/0 | 4611 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0019t0014 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4621): Show |
chr3 | 149124638 | 149178732 |
| a0001c0021t0002 | 0/0 | 4615 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0001c0022t0001 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0023t0001 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0001c0024t0001 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0002c0007t0003 | 0/0 | 4611 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0002c0007t0005 | 0/0 | 4617 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4612): Show |
chr3 | 149124638 | 149178732 |
| a0003c0008t0001 | 0/0 | 4611 | 3 | 3 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0004c0009t0003 | 0/0 | 4611 | 3 | 0 | 0 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0005c0010t0002 | 0/0 | 4615 | 3 | 0 | 0 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4610): Show |
chr3 | 149124638 | 149178732 |
| a0006c0020t0024 | 0/0 | 4623 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4618): Show |
chr3 | 149124638 | 149178732 |
| a0007c0017t0001 | 0/0 | 4611 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0008c0026t0005 | 0/0 | 4617 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4612): Show |
chr3 | 149124638 | 149178732 |
| a0009c0027t0013 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4607): Show |
chr3 | 149124638 | 149178732 |
| a0010c0016t0039 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| a0011c0025t0001 | 0/0 | 4611 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | GGAAG others(4606): Show |
chr3 | 149124638 | 149178732 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0005g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0011g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0038g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0041g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0001t0042g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0008g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0009g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0009g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0013g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0016g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0016g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0016g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0017g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0017g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0017g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0021g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0027g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0029g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0030g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0032g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0034g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0035g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0002t0037g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0004 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0009g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0015g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0018g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0020g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0022g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0003t0022g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0004t0025g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0006g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0010g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0012g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0012g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0015g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0018g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0019g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0019g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0023g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0026g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0028g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0031g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0033g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0036g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0005t0040g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0006t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0006t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0006t0011g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0006t0011g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0006t0011g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0011t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0011t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0012t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0013t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0014t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0015t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0018t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0019t0014g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0021t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0022t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0023t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0001c0024t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0002c0007t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0002c0007t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0002c0007t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0003c0008t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0003c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0004c0009t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0004c0009t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0005c0010t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0006c0020t0024g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0007c0017t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0008c0026t0005g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0009c0027t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0010c0016t0039g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| a0011c0025t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0019 | EUR | GBR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0270 | EUR | GBR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0255 | EUR | FIN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00280 | hp2 | a0001 | c0002 | t0016 | g0028 | EUR | FIN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00323 | hp1 | a0001 | c0002 | t0009 | g0160 | EUR | FIN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00323 | hp2 | a0001 | c0004 | t0004 | g0124 | EUR | FIN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00438 | hp1 | a0001 | c0004 | t0002 | g0011 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00558 | hp2 | a0001 | c0004 | t0002 | g0083 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00597 | hp1 | a0001 | c0003 | t0020 | g0253 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00621 | hp2 | a0001 | c0004 | t0005 | g0092 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0265 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00735 | hp2 | a0001 | c0001 | t0011 | g0215 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG00738 | hp2 | a0001 | c0002 | t0010 | g0048 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01069 | hp1 | a0001 | c0002 | t0008 | g0060 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01069 | hp2 | a0001 | c0002 | t0008 | g0185 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01070 | hp1 | a0001 | c0002 | t0016 | g0178 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01071 | hp1 | a0001 | c0002 | t0016 | g0030 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01071 | hp2 | a0001 | c0002 | t0008 | g0059 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0102 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01081 | hp1 | a0001 | c0002 | t0009 | g0029 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0012 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01167 | hp1 | a0001 | c0005 | t0018 | g0072 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0195 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01175 | hp1 | a0001 | c0004 | t0002 | g0101 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01192 | hp1 | a0001 | c0002 | t0008 | g0054 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01192 | hp2 | a0001 | c0003 | t0018 | g0069 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0242 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01243 | hp2 | a0001 | c0005 | t0012 | g0010 | AMR | PUR | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01255 | hp1 | a0001 | c0005 | t0010 | g0288 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01255 | hp2 | a0001 | c0004 | t0004 | g0122 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0194 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01346 | hp2 | a0001 | c0005 | t0023 | g0074 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01358 | hp1 | a0006 | c0020 | t0024 | g0073 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0208 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01433 | hp1 | a0001 | c0005 | t0006 | g0290 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01433 | hp2 | a0001 | c0004 | t0002 | g0002 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0250 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0296 | EUR | IBS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01516 | hp2 | a0001 | c0003 | t0022 | g0277 | EUR | IBS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01517 | hp1 | a0001 | c0003 | t0022 | g0276 | EUR | IBS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01884 | hp2 | a0001 | c0005 | t0014 | g0291 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0248 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0157 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01928 | hp1 | a0007 | c0017 | t0001 | g0206 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01928 | hp2 | a0001 | c0021 | t0002 | g0267 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0252 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01975 | hp1 | a0001 | c0004 | t0002 | g0099 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01975 | hp2 | a0008 | c0026 | t0005 | g0001 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02055 | hp1 | a0001 | c0005 | t0036 | g0292 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02055 | hp2 | a0001 | c0002 | t0006 | g0159 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02056 | hp1 | a0001 | c0003 | t0020 | g0039 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0263 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02074 | hp1 | a0001 | c0015 | t0001 | g0213 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0023 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02080 | hp2 | a0001 | c0004 | t0004 | g0007 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02083 | hp2 | a0001 | c0004 | t0005 | g0104 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02129 | hp1 | a0001 | c0004 | t0004 | g0002 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0176 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02135 | hp2 | a0001 | c0004 | t0002 | g0002 | EAS | KHV | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0283 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02145 | hp2 | a0001 | c0002 | t0006 | g0158 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02148 | hp2 | a0001 | c0004 | t0002 | g0007 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CDX | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02155 | hp2 | a0001 | c0003 | t0007 | g0005 | EAS | CDX | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | CDX | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02257 | hp1 | a0001 | c0002 | t0011 | g0284 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0148 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0280 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02273 | hp1 | a0001 | c0006 | t0001 | g0144 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02280 | hp1 | a0001 | c0002 | t0029 | g0067 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0244 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02293 | hp2 | a0001 | c0003 | t0009 | g0228 | AMR | PEL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02451 | hp1 | a0001 | c0002 | t0034 | g0047 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0156 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02572 | hp1 | a0001 | c0002 | t0032 | g0128 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0046 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02602 | hp1 | a0001 | c0004 | t0002 | g0103 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02602 | hp2 | a0001 | c0002 | t0009 | g0029 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0281 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02615 | hp2 | a0001 | c0005 | t0015 | g0041 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02622 | hp2 | a0001 | c0002 | t0035 | g0065 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0169 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02630 | hp2 | a0001 | c0003 | t0007 | g0042 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0247 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02683 | hp2 | a0001 | c0002 | t0030 | g0145 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02698 | hp2 | a0001 | c0006 | t0011 | g0142 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02717 | hp1 | a0002 | c0007 | t0003 | g0020 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02717 | hp2 | a0001 | c0003 | t0007 | g0295 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02735 | hp1 | a0001 | c0018 | t0001 | g0053 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02735 | hp2 | a0001 | c0006 | t0011 | g0146 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0084 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02809 | hp1 | a0001 | c0005 | t0015 | g0041 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02809 | hp2 | a0001 | c0003 | t0007 | g0018 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02818 | hp1 | a0001 | c0003 | t0007 | g0174 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02818 | hp2 | a0001 | c0019 | t0014 | g0297 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02886 | hp1 | a0002 | c0007 | t0005 | g0238 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02886 | hp2 | a0001 | c0003 | t0007 | g0042 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0294 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02896 | hp1 | a0001 | c0003 | t0004 | g0243 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02896 | hp2 | a0001 | c0002 | t0010 | g0045 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02922 | hp1 | a0001 | c0005 | t0033 | g0024 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0170 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02965 | hp2 | a0001 | c0005 | t0012 | g0289 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02970 | hp1 | a0002 | c0007 | t0005 | g0079 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02970 | hp2 | a0001 | c0005 | t0006 | g0024 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03017 | hp1 | a0001 | c0001 | t0041 | g0111 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03017 | hp2 | a0001 | c0004 | t0002 | g0298 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03041 | hp1 | a0001 | c0005 | t0031 | g0286 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03098 | hp1 | a0001 | c0005 | t0003 | g0246 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0175 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03130 | hp1 | a0003 | c0008 | t0001 | g0037 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03130 | hp2 | a0001 | c0002 | t0010 | g0044 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03139 | hp1 | a0001 | c0005 | t0006 | g0136 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03195 | hp1 | a0001 | c0002 | t0013 | g0009 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0168 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03225 | hp2 | a0001 | c0003 | t0007 | g0293 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03239 | hp1 | a0001 | c0004 | t0025 | g0070 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0236 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03453 | hp2 | a0001 | c0005 | t0019 | g0134 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03486 | hp1 | a0001 | c0003 | t0007 | g0018 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03490 | hp1 | a0001 | c0006 | t0011 | g0141 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0205 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03491 | hp2 | a0001 | c0011 | t0001 | g0008 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0151 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03516 | hp2 | a0001 | c0005 | t0005 | g0137 | AFR | ESN | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03540 | hp2 | a0002 | c0007 | t0003 | g0020 | AFR | GWD | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03579 | hp1 | a0001 | c0005 | t0019 | g0135 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0249 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03654 | hp2 | a0001 | c0002 | t0017 | g0052 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03669 | hp1 | a0001 | c0002 | t0008 | g0050 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03669 | hp2 | a0001 | c0004 | t0005 | g0114 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03688 | hp1 | a0001 | c0005 | t0026 | g0071 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03688 | hp2 | a0001 | c0002 | t0008 | g0186 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03704 | hp1 | a0001 | c0003 | t0005 | g0005 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03704 | hp2 | a0001 | c0004 | t0002 | g0022 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03710 | hp1 | a0001 | c0011 | t0001 | g0117 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03710 | hp2 | a0001 | c0002 | t0008 | g0051 | SAS | PJL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03927 | hp2 | a0001 | c0002 | t0008 | g0064 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03942 | hp1 | a0001 | c0002 | t0008 | g0063 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04115 | hp1 | a0001 | c0004 | t0004 | g0126 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04115 | hp2 | a0001 | c0002 | t0008 | g0061 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0004 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04184 | hp2 | a0001 | c0002 | t0017 | g0062 | SAS | BEB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04204 | hp1 | a0001 | c0006 | t0001 | g0143 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04228 | hp1 | a0001 | c0002 | t0017 | g0057 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG04228 | hp2 | a0001 | c0004 | t0002 | g0094 | SAS | STU | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0241 | AFR | YRI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18522 | hp2 | a0001 | c0002 | t0013 | g0009 | AFR | YRI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18612 | hp1 | a0001 | c0004 | t0002 | g0081 | EAS | CHB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18612 | hp2 | a0001 | c0012 | t0002 | g0077 | EAS | CHB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | CHB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18906 | hp1 | a0001 | c0005 | t0014 | g0010 | AFR | YRI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0130 | AFR | YRI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18939 | hp2 | a0001 | c0004 | t0006 | g0022 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18941 | hp2 | a0001 | c0003 | t0009 | g0239 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18942 | hp1 | a0001 | c0002 | t0009 | g0155 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18942 | hp2 | a0001 | c0003 | t0009 | g0254 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18943 | hp1 | a0004 | c0009 | t0003 | g0167 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18943 | hp2 | a0001 | c0023 | t0001 | g0005 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18944 | hp1 | a0001 | c0024 | t0001 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18944 | hp2 | a0001 | c0004 | t0004 | g0105 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18945 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18947 | hp1 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18952 | hp1 | a0010 | c0016 | t0039 | g0138 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0089 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18960 | hp1 | a0001 | c0004 | t0004 | g0109 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18962 | hp2 | a0005 | c0010 | t0002 | g0013 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18964 | hp1 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18965 | hp1 | a0001 | c0004 | t0002 | g0097 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18965 | hp2 | a0001 | c0003 | t0004 | g0262 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18967 | hp1 | a0001 | c0004 | t0002 | g0091 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18968 | hp2 | a0001 | c0004 | t0002 | g0086 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18970 | hp2 | a0001 | c0003 | t0009 | g0039 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0095 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18972 | hp1 | a0001 | c0013 | t0001 | g0225 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18972 | hp2 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18973 | hp1 | a0001 | c0022 | t0001 | g0005 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18974 | hp2 | a0001 | c0004 | t0002 | g0011 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18979 | hp1 | a0001 | c0004 | t0002 | g0076 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18981 | hp1 | a0001 | c0003 | t0004 | g0278 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18983 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18983 | hp2 | a0001 | c0001 | t0042 | g0087 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18984 | hp1 | a0001 | c0004 | t0002 | g0093 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18990 | hp2 | a0001 | c0004 | t0004 | g0090 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18993 | hp2 | a0001 | c0004 | t0002 | g0080 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18998 | hp1 | a0001 | c0004 | t0002 | g0118 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19000 | hp1 | a0001 | c0004 | t0002 | g0082 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0271 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19007 | hp1 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19009 | hp1 | a0004 | c0009 | t0003 | g0003 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19010 | hp2 | a0011 | c0025 | t0001 | g0275 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19011 | hp2 | a0001 | c0003 | t0009 | g0272 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19012 | hp1 | a0001 | c0004 | t0002 | g0107 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19012 | hp2 | a0001 | c0002 | t0021 | g0166 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | LWK | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | LWK | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19043 | hp1 | a0001 | c0002 | t0013 | g0009 | AFR | LWK | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19043 | hp2 | a0001 | c0003 | t0015 | g0120 | AFR | LWK | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19056 | hp2 | a0001 | c0003 | t0004 | g0269 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19057 | hp2 | a0001 | c0004 | t0002 | g0011 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0258 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19058 | hp2 | a0001 | c0004 | t0002 | g0096 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19059 | hp1 | a0001 | c0004 | t0001 | g0123 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19060 | hp1 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19063 | hp1 | a0001 | c0004 | t0002 | g0023 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19063 | hp2 | a0005 | c0010 | t0002 | g0013 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19066 | hp1 | a0004 | c0009 | t0003 | g0003 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19066 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19072 | hp1 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19072 | hp2 | a0001 | c0004 | t0002 | g0108 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19085 | hp2 | a0005 | c0010 | t0002 | g0013 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19086 | hp1 | a0001 | c0004 | t0005 | g0106 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19089 | hp1 | a0001 | c0004 | t0001 | g0125 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0119 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19091 | hp2 | a0001 | c0014 | t0009 | g0251 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19240 | hp1 | a0003 | c0008 | t0001 | g0240 | AFR | YRI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | YRI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0273 | EUR | TSI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0055 | EUR | TSI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20805 | hp1 | a0001 | c0001 | t0038 | g0001 | EUR | TSI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0256 | EUR | TSI | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0014 | SAS | GIH | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | GIH | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01123 | hp1 | a0001 | c0002 | t0037 | g0028 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0237 | AMR | CLM | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02109 | hp1 | a0001 | c0002 | t0012 | g0129 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02109 | hp2 | a0001 | c0002 | t0010 | g0043 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02486 | hp1 | a0001 | c0002 | t0006 | g0150 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02486 | hp2 | a0001 | c0005 | t0003 | g0285 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0279 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG02559 | hp2 | a0003 | c0008 | t0001 | g0037 | AFR | ACB | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03471 | hp1 | a0001 | c0005 | t0012 | g0010 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG03471 | hp2 | a0001 | c0002 | t0006 | g0149 | AFR | MSL | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG06807 | hp1 | a0009 | c0027 | t0013 | g0009 | AFR | USA | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| HG06807 | hp2 | a0001 | c0002 | t0027 | g0121 | AFR | USA | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18955 | hp1 | a0001 | c0004 | t0002 | g0088 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20300 | hp1 | a0001 | c0005 | t0028 | g0010 | AFR | USA | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA20300 | hp2 | a0001 | c0004 | t0008 | g0098 | AFR | USA | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | LWK | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| NA21309 | hp2 | a0001 | c0005 | t0040 | g0287 | AFR | LWK | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0002 | g0100 | REF | REF | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0078 | REF | REF | HPS3_chr3_149124638_149178732 | HPS3 | chr3 | 149124638 | 149178732 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149129881 | A | G | 1 | a0005 | 3 | NA18962.hp2 NA19063.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.158A>G | p.Gln53Arg | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/17 | 244/4611 | 158/3015 | 53/1004 | chr3 | 149129881 | |||
| chr3:149140031 | A | G | 1 | a0009 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.245A>G | p.Lys82Arg | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/17 | 331/4611 | 245/3015 | 82/1004 | chr3 | 149140031 | |||
| chr3:149140178 | C | T | 1 | a0008 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.392C>T | p.Pro131Leu | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/17 | 478/4611 | 392/3015 | 131/1004 | chr3 | 149140178 | |||
| chr3:149140184 | C | T | 1 | a0004 | 3 | NA18943.hp1 NA19009.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.398C>T | p.Ser133Leu | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/17 | 484/4611 | 398/3015 | 133/1004 | chr3 | 149140184 | |||
| chr3:149140463 | A | G | 1 | a0011 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.677A>G | p.His226Arg | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/17 | 763/4611 | 677/3015 | 226/1004 | chr3 | 149140463 | |||
| chr3:149141127 | G | A | 1 | a0003 | 3 | HG02559.hp2 HG03130.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.823G>A | p.Glu275Lys | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/17 | 909/4611 | 823/3015 | 275/1004 | chr3 | 149141127 | |||
| chr3:149153614 | A | G | 1 | a0002 | 4 | HG02717.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.1366A>G | p.Ile456Val | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/17 | 1452/4611 | 1366/3015 | 456/1004 | chr3 | 149153614 | |||
| chr3:149158685 | C | T | 1 | a0005 | 3 | NA18962.hp2 NA19063.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.1711C>T | p.His571Tyr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/17 | 1797/4611 | 1711/3015 | 571/1004 | chr3 | 149158685 | |||
| chr3:149162256 | G | A | 1 | a0006 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.2215G>A | p.Gly739Arg | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 12/17 | 2301/4611 | 2215/3015 | 739/1004 | chr3 | 149162256 | |||
| chr3:149163924 | A | G | 1 | a0007 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.2564A>G | p.Tyr855Cys | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/17 | 2650/4611 | 2564/3015 | 855/1004 | chr3 | 149163924 | |||
| chr3:149167143 | G | A | 1 | a0010 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.2699G>A | p.Arg900His | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 15/17 | 2785/4611 | 2699/3015 | 900/1004 | chr3 | 149167143 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149129759 | G | C | 1 | a0001c0012 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.36G>C | p.Ser12Ser | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/17 | 122/4611 | 36/3015 | 12/1004 | chr3 | 149129759 | |||
| chr3:149129858 | G | C | 1 | a0001c0013 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.135G>C | p.Ala45Ala | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/17 | 221/4611 | 135/3015 | 45/1004 | chr3 | 149129858 | |||
| chr3:149141349 | T | C | 1 | a0001c0014 | 1 | NA19091.hp2 | synonymous_variant | LOW | c.939T>C | p.His313His | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/17 | 1025/4611 | 939/3015 | 313/1004 | chr3 | 149141349 | |||
| chr3:149141379 | C | T | 1 | a0001c0024 | 1 | NA18944.hp1 | splice_region_variant&synonymous_variant | LOW | c.969C>T | p.Thr323Thr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/17 | 1055/4611 | 969/3015 | 323/1004 | chr3 | 149141379 | |||
| chr3:149145364 | A | G | 10 | a0001c0003 a0001c0005 a0001c0014 others(7): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
synonymous_variant | LOW | c.981A>G | p.Thr327Thr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/17 | 1067/4611 | 981/3015 | 327/1004 | chr3 | 149145364 | |||
| chr3:149145520 | G | A | 1 | a0001c0015 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1137G>A | p.Thr379Thr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/17 | 1223/4611 | 1137/3015 | 379/1004 | chr3 | 149145520 | |||
| chr3:149145544 | A | G | 1 | a0001c0018 | 1 | HG02735.hp1 | splice_region_variant&synonymous_variant | LOW | c.1161A>G | p.Thr387Thr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/17 | 1247/4611 | 1161/3015 | 387/1004 | chr3 | 149145544 | |||
| chr3:149155185 | G | A | 2 | a0001c0006 a0001c0019 |
6 | HG02273.hp1 HG02698.hp2 HG02735.hp2 others(3): Show |
synonymous_variant | LOW | c.1479G>A | p.Thr493Thr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/17 | 1565/4611 | 1479/3015 | 493/1004 | chr3 | 149155185 | |||
| chr3:149155200 | G | A | 13 | a0001c0002 a0001c0004 a0001c0005 others(10): Show |
192 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
synonymous_variant | LOW | c.1494G>A | p.Gln498Gln | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/17 | 1580/4611 | 1494/3015 | 498/1004 | chr3 | 149155200 | |||
| chr3:149158747 | G | A | 1 | a0001c0011 | 2 | HG03491.hp2 HG03710.hp1 |
synonymous_variant | LOW | c.1773G>A | p.Thr591Thr | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/17 | 1859/4611 | 1773/3015 | 591/1004 | chr3 | 149158747 | |||
| chr3:149158759 | A | G | 1 | a0001c0023 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.1785A>G | p.Val595Val | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/17 | 1871/4611 | 1785/3015 | 595/1004 | chr3 | 149158759 | |||
| chr3:149162237 | C | T | 1 | a0001c0022 | 1 | NA18973.hp1 | synonymous_variant | LOW | c.2196C>T | p.His732His | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 12/17 | 2282/4611 | 2196/3015 | 732/1004 | chr3 | 149162237 | |||
| chr3:149163886 | C | T | 4 | a0001c0004 a0001c0012 a0001c0021 others(1): Show |
66 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
synonymous_variant | LOW | c.2526C>T | p.His842His | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/17 | 2612/4611 | 2526/3015 | 842/1004 | chr3 | 149163886 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149129654 | T | C | 6 | a0001c0003t0018 a0001c0004t0025 a0001c0005t0018 others(3): Show |
6 | HG01167.hp1 HG01192.hp2 HG01346.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-70T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/17 | 70 | chr3 | 149129654 | ||||||
| chr3:149129684 | T | C | 1 | a0001c0002t0027 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/17 | 40 | chr3 | 149129684 | ||||||
| chr3:149129687 | A | G | 1 | a0001c0001t0042 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/17 | 37 | chr3 | 149129687 | ||||||
| chr3:149172318 | T | TCA | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0004 others(3): Show |
29 | HG00323.hp2 HG00597.hp1 HG01167.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*134dupCA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACA | 10 | a0001c0001t0002 a0001c0001t0042 a0001c0002t0002 others(7): Show |
60 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*131_*134dupCACA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACA | 7 | a0001c0001t0005 a0001c0003t0005 a0001c0004t0005 others(4): Show |
20 | HG00621.hp2 HG01257.hp1 HG01975.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*129_*134dupCACACA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACAC others(1): Show |
6 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 others(3): Show |
17 | HG00738.hp2 HG01255.hp1 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*127_*134dupCACACA others(2): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACAC others(3): Show |
3 | a0001c0002t0032 a0001c0002t0034 a0001c0005t0033 |
3 | HG02451.hp1 HG02572.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125_*134dupCACACA others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACAC others(5): Show |
3 | a0001c0002t0012 a0001c0005t0012 a0006c0020t0024 |
5 | HG01243.hp2 HG01358.hp1 HG02109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*123_*134dupCACACA others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACAC others(7): Show |
5 | a0001c0002t0030 a0001c0005t0014 a0001c0005t0023 others(2): Show |
6 | HG01346.hp2 HG01884.hp2 HG02683.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*121_*134dupCACACA others(8): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACAC others(9): Show |
1 | a0001c0002t0029 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119_*134dupCACACA others(10): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCACACAC others(13): Show |
1 | a0001c0005t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*115_*134dupCACACA others(14): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCTCACAC others(1): Show |
3 | a0001c0001t0008 a0001c0002t0008 a0001c0004t0008 |
12 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*97_*98insTCACACAC | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 98 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCTCACAC others(3): Show |
1 | a0001c0002t0017 | 3 | HG03654.hp2 HG04184.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*97_*98insTCACACAC others(2): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 98 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCTCACAC others(5): Show |
1 | a0001c0001t0041 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*97_*98insTCACACAC others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 98 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | T | TCTCACAC others(9): Show |
1 | a0001c0005t0026 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*97_*98insTCACACAC others(8): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 98 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | TCA | T | 5 | a0001c0001t0007 a0001c0001t0011 a0001c0002t0011 others(2): Show |
17 | HG00735.hp2 HG02155.hp2 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*134delCA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 133 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172318 | TCACACAC others(11): Show |
T | 1 | a0001c0005t0040 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*134delCACACA others(12): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 117 | INFO_REALIGN_3_PRIME | chr3 | 149172318 | |||||
| chr3:149172350 | A | ACG | 2 | a0001c0002t0016 a0001c0002t0027 |
4 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*129_*130insGC | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 130 | INFO_REALIGN_3_PRIME | chr3 | 149172350 | |||||
| chr3:149172350 | A | G | 9 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 others(6): Show |
49 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 128 | chr3 | 149172350 | ||||||
| chr3:149172357 | T | C | 3 | a0001c0003t0015 a0001c0005t0015 a0001c0005t0036 |
4 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*135T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 135 | chr3 | 149172357 | ||||||
| chr3:149172394 | G | A | 12 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 others(9): Show |
54 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*172G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 172 | chr3 | 149172394 | ||||||
| chr3:149172557 | G | A | 4 | a0001c0002t0009 a0001c0003t0009 a0001c0003t0020 others(1): Show |
12 | HG00323.hp1 HG00597.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*335G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 335 | chr3 | 149172557 | ||||||
| chr3:149172633 | A | T | 1 | a0001c0005t0031 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 411 | chr3 | 149172633 | ||||||
| chr3:149172802 | G | C | 2 | a0001c0001t0021 a0001c0002t0021 |
2 | NA18945.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 580 | chr3 | 149172802 | ||||||
| chr3:149172835 | T | G | 3 | a0001c0003t0015 a0001c0005t0015 a0001c0005t0036 |
4 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*613T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 613 | chr3 | 149172835 | ||||||
| chr3:149172885 | A | AT | 17 | a0001c0002t0010 a0001c0002t0012 a0001c0002t0013 others(14): Show |
27 | HG00738.hp2 HG01243.hp2 HG01255.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*668dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 669 | INFO_REALIGN_3_PRIME | chr3 | 149172885 | |||||
| chr3:149172945 | C | T | 29 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 others(26): Show |
81 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*723C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 723 | chr3 | 149172945 | ||||||
| chr3:149172946 | A | G | 4 | a0001c0002t0013 a0001c0002t0035 a0001c0005t0040 others(1): Show |
6 | HG02622.hp2 HG03195.hp1 HG06807.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*724A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 724 | chr3 | 149172946 | ||||||
| chr3:149173205 | T | G | 1 | a0001c0003t0022 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*983T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 983 | chr3 | 149173205 | ||||||
| chr3:149173208 | G | T | 1 | a0010c0016t0039 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*986G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 986 | chr3 | 149173208 | ||||||
| chr3:149173240 | A | G | 2 | a0001c0002t0013 a0009c0027t0013 |
4 | HG03195.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1018A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 1018 | chr3 | 149173240 | ||||||
| chr3:149173341 | G | C | 1 | a0001c0001t0038 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1119G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 1119 | chr3 | 149173341 | ||||||
| chr3:149173455 | G | A | 1 | a0001c0002t0032 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 1233 | chr3 | 149173455 | ||||||
| chr3:149173577 | G | A | 4 | a0001c0002t0030 a0001c0005t0023 a0001c0005t0026 others(1): Show |
4 | HG01346.hp2 HG01358.hp1 HG02683.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1355G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 17/17 | 1355 | chr3 | 149173577 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149130012 | TG | T | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+75delG | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149130012 | ||||||
| chr3:149130062 | C | T | 1 | a0001c0004t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217+122C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130062 | |||||||
| chr3:149130072 | C | T | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+132C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130072 | |||||||
| chr3:149130147 | G | T | 10 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(7): Show |
13 | HG01516.hp1 HG02055.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.217+207G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130147 | |||||||
| chr3:149130180 | C | A | 16 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.217+240C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130180 | |||||||
| chr3:149130286 | C | G | 16 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.217+346C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130286 | |||||||
| chr3:149130407 | C | T | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.217+467C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130407 | |||||||
| chr3:149130563 | C | T | 3 | a0001c0002t0001g0282 a0001c0002t0003g0283 a0001c0002t0011g0284 |
3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.217+623C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130563 | |||||||
| chr3:149130616 | C | G | 68 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0038 others(65): Show |
78 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.217+676C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130616 | |||||||
| chr3:149130703 | C | G | 3 | a0001c0003t0002g0280 a0001c0003t0002g0281 a0001c0005t0001g0279 |
3 | HG02258.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.217+763C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130703 | |||||||
| chr3:149130787 | G | T | 1 | a0001c0003t0004g0278 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.217+847G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149130787 | |||||||
| chr3:149131114 | G | A | 9 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(6): Show |
12 | HG01516.hp1 HG02055.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+1174G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131114 | |||||||
| chr3:149131122 | T | TA | 17 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0010g0048 others(14): Show |
19 | HG00099.hp1 HG00738.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+1200dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149131122 | ||||||
| chr3:149131122 | T | TAA | 6 | a0001c0002t0001g0049 a0001c0002t0006g0046 a0001c0002t0010g0043 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+1199_217+1200d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149131122 | ||||||
| chr3:149131122 | TA | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(134): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.217+1200delA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149131122 | ||||||
| chr3:149131134 | A | C | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+1194A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131134 | |||||||
| chr3:149131135 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(136): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.217+1195A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131135 | |||||||
| chr3:149131136 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(79): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.217+1196A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131136 | |||||||
| chr3:149131139 | A | T | 1 | a0001c0003t0001g0040 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.217+1199A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131139 | |||||||
| chr3:149131140 | AC | A | 30 | a0001c0002t0001g0282 a0001c0002t0003g0283 a0001c0002t0011g0284 others(27): Show |
31 | HG00597.hp1 HG01243.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.217+1201delC | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131140 | |||||||
| chr3:149131141 | C | A | 74 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(71): Show |
84 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.217+1201C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131141 | |||||||
| chr3:149131142 | A | G | 1 | a0001c0002t0027g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.217+1202A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131142 | |||||||
| chr3:149131235 | C | T | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+1295C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131235 | |||||||
| chr3:149131302 | T | C | 3 | a0001c0002t0001g0282 a0001c0002t0003g0283 a0001c0002t0011g0284 |
3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.217+1362T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131302 | |||||||
| chr3:149131325 | C | T | 118 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0003g0066 others(115): Show |
131 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.217+1385C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131325 | |||||||
| chr3:149131347 | C | T | 2 | a0001c0003t0022g0276 a0001c0003t0022g0277 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.217+1407C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131347 | |||||||
| chr3:149131352 | CTG | C | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+1417_217+1418d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149131352 | ||||||
| chr3:149131476 | C | T | 113 | a0001c0001t0001g0127 a0001c0002t0001g0049 a0001c0002t0001g0055 others(110): Show |
126 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.217+1536C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131476 | |||||||
| chr3:149131597 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.217+1657G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131597 | |||||||
| chr3:149131784 | C | T | 3 | a0001c0002t0004g0130 a0001c0002t0012g0129 a0001c0002t0032g0128 |
3 | HG02109.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.217+1844C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131784 | |||||||
| chr3:149131821 | G | A | 1 | a0002c0007t0005g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.217+1881G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149131821 | |||||||
| chr3:149132024 | T | G | 81 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0001g0282 others(78): Show |
93 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.217+2084T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149132024 | |||||||
| chr3:149132087 | A | T | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.217+2147A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149132087 | |||||||
| chr3:149132093 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.217+2153G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149132093 | |||||||
| chr3:149132425 | A | G | 3 | a0001c0002t0001g0282 a0001c0002t0003g0283 a0001c0002t0011g0284 |
3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.217+2485A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149132425 | |||||||
| chr3:149133013 | G | A | 4 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+3073G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133013 | |||||||
| chr3:149133169 | C | T | 3 | a0001c0002t0001g0282 a0001c0002t0003g0283 a0001c0002t0011g0284 |
3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.217+3229C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133169 | |||||||
| chr3:149133203 | T | C | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+3263T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133203 | |||||||
| chr3:149133284 | T | A | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+3344T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133284 | |||||||
| chr3:149133304 | A | AT | 5 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0029g0067 others(2): Show |
5 | HG02280.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+3368dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149133304 | ||||||
| chr3:149133309 | A | T | 5 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0029g0067 others(2): Show |
5 | HG02280.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+3369A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133309 | |||||||
| chr3:149133384 | C | A | 1 | a0001c0003t0009g0239 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.217+3444C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133384 | |||||||
| chr3:149133430 | C | A | 2 | a0001c0002t0008g0050 a0001c0002t0008g0051 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.217+3490C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133430 | |||||||
| chr3:149133446 | G | A | 16 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.217+3506G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133446 | |||||||
| chr3:149133714 | T | C | 3 | a0001c0002t0008g0050 a0001c0002t0008g0051 a0001c0002t0017g0052 |
3 | HG03654.hp2 HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.217+3774T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133714 | |||||||
| chr3:149133720 | G | A | 2 | a0001c0002t0001g0282 a0001c0002t0003g0283 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.217+3780G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133720 | |||||||
| chr3:149133802 | G | T | 1 | a0001c0002t0011g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.217+3862G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133802 | |||||||
| chr3:149133839 | T | TA | 3 | a0001c0002t0001g0140 a0001c0002t0003g0139 a0010c0016t0039g0138 |
3 | NA18952.hp1 NA19075.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.217+3901dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149133839 | ||||||
| chr3:149133844 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0180 |
3 | NA18949.hp2 NA18973.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.217+3904G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133844 | |||||||
| chr3:149133878 | C | T | 4 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+3938C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133878 | |||||||
| chr3:149133988 | T | A | 6 | a0001c0002t0030g0145 a0001c0006t0001g0143 a0001c0006t0001g0144 others(3): Show |
6 | HG02273.hp1 HG02683.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+4048T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133988 | |||||||
| chr3:149133988 | T | TA | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+4056dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149133988 | ||||||
| chr3:149133988 | T | TTA | 7 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(4): Show |
9 | HG01516.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.217+4048_217+4049i others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133988 | |||||||
| chr3:149133989 | A | T | 11 | a0001c0004t0001g0119 a0001c0005t0003g0285 a0001c0005t0006g0290 others(8): Show |
12 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.217+4049A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149133989 | |||||||
| chr3:149134131 | A | G | 1 | a0001c0005t0001g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217+4191A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149134131 | |||||||
| chr3:149134158 | C | T | 1 | a0011c0025t0001g0275 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.217+4218C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149134158 | |||||||
| chr3:149134183 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.217+4243T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149134183 | |||||||
| chr3:149134375 | T | A | 1 | a0003c0008t0001g0240 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217+4435T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149134375 | |||||||
| chr3:149134377 | A | T | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+4437A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149134377 | |||||||
| chr3:149134382 | G | GAGAA | 4 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+4450_217+4453d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149134382 | ||||||
| chr3:149134382 | GAGAA | G | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+4450_217+4453d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149134382 | ||||||
| chr3:149134668 | G | A | 116 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0003g0066 others(113): Show |
129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.217+4728G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149134668 | |||||||
| chr3:149135031 | C | T | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-4973C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135031 | |||||||
| chr3:149135173 | T | C | 2 | a0001c0002t0001g0282 a0001c0002t0003g0283 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-4831T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135173 | |||||||
| chr3:149135177 | T | G | 1 | a0001c0005t0003g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218-4827T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135177 | |||||||
| chr3:149135273 | A | G | 1 | a0001c0003t0001g0274 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.218-4731A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135273 | |||||||
| chr3:149135442 | G | A | 1 | a0001c0004t0004g0122 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.218-4562G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135442 | |||||||
| chr3:149135504 | G | A | 2 | a0001c0004t0002g0076 a0001c0012t0002g0077 |
2 | NA18612.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.218-4500G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135504 | |||||||
| chr3:149135530 | T | C | 2 | a0001c0002t0001g0282 a0001c0002t0003g0283 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-4474T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135530 | |||||||
| chr3:149135532 | A | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(69): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.218-4472A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135532 | |||||||
| chr3:149135557 | A | T | 1 | a0001c0003t0001g0274 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.218-4447A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135557 | |||||||
| chr3:149135690 | T | C | 189 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(186): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.218-4314T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135690 | |||||||
| chr3:149135723 | G | T | 1 | a0001c0004t0002g0118 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.218-4281G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135723 | |||||||
| chr3:149135825 | G | A | 3 | a0001c0002t0006g0148 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02258.hp1 HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.218-4179G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149135825 | |||||||
| chr3:149136129 | C | G | 1 | a0001c0002t0008g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.218-3875C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136129 | |||||||
| chr3:149136177 | C | T | 16 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.218-3827C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136177 | |||||||
| chr3:149136205 | CAT | C | 189 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(186): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.218-3789_218-3788d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149136205 | ||||||
| chr3:149136312 | G | A | 237 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(234): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.218-3692G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136312 | |||||||
| chr3:149136348 | G | A | 66 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(63): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.218-3656G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136348 | |||||||
| chr3:149136418 | C | T | 6 | a0001c0003t0018g0069 a0001c0004t0025g0070 a0001c0005t0018g0072 others(3): Show |
6 | HG01167.hp1 HG01192.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-3586C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136418 | |||||||
| chr3:149136428 | T | G | 175 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(172): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.218-3576T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136428 | |||||||
| chr3:149136482 | G | T | 66 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(63): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.218-3522G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136482 | |||||||
| chr3:149136514 | T | TA | 3 | a0002c0007t0003g0020 a0002c0007t0005g0079 a0002c0007t0005g0238 |
4 | HG02717.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-3487dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149136514 | ||||||
| chr3:149136567 | C | T | 1 | a0001c0003t0001g0273 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.218-3437C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136567 | |||||||
| chr3:149136602 | T | C | 2 | a0001c0002t0001g0282 a0001c0002t0003g0283 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-3402T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136602 | |||||||
| chr3:149136644 | G | A | 237 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(234): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.218-3360G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136644 | |||||||
| chr3:149136718 | A | C | 9 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(6): Show |
12 | HG01516.hp1 HG02055.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-3286A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136718 | |||||||
| chr3:149136881 | G | T | 42 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0040 others(39): Show |
49 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.218-3123G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136881 | |||||||
| chr3:149136942 | G | A | 1 | a0001c0002t0003g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.218-3062G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149136942 | |||||||
| chr3:149137000 | T | A | 6 | a0001c0001t0001g0152 a0001c0002t0001g0140 a0001c0002t0003g0139 others(3): Show |
6 | NA18952.hp1 NA18980.hp1 NA19064.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-3004T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137000 | |||||||
| chr3:149137035 | A | G | 1 | a0001c0002t0011g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-2969A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137035 | |||||||
| chr3:149137317 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.218-2687G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137317 | |||||||
| chr3:149137559 | G | A | 57 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0038 others(54): Show |
66 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.218-2445G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137559 | |||||||
| chr3:149137809 | G | T | 1 | a0001c0001t0005g0235 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.218-2195G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137809 | |||||||
| chr3:149137810 | A | C | 9 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(6): Show |
12 | HG01516.hp1 HG02055.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-2194A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137810 | |||||||
| chr3:149137813 | G | A | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-2191G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137813 | |||||||
| chr3:149137902 | C | G | 1 | a0001c0002t0006g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218-2102C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149137902 | |||||||
| chr3:149137998 | A | AATTT | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.218-1996_218-1993d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149137998 | ||||||
| chr3:149137998 | AATTT | A | 7 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0011g0284 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-1996_218-1993d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 149137998 | ||||||
| chr3:149138191 | G | A | 1 | a0001c0019t0014g0297 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.218-1813G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138191 | |||||||
| chr3:149138331 | T | C | 6 | a0001c0003t0018g0069 a0001c0004t0025g0070 a0001c0005t0018g0072 others(3): Show |
6 | HG01167.hp1 HG01192.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-1673T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138331 | |||||||
| chr3:149138389 | A | T | 4 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-1615A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138389 | |||||||
| chr3:149138417 | G | A | 1 | a0001c0002t0009g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.218-1587G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138417 | |||||||
| chr3:149138534 | G | A | 4 | a0001c0004t0002g0011 a0001c0004t0002g0081 a0001c0004t0002g0082 others(1): Show |
6 | HG00438.hp1 HG00558.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-1470G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138534 | |||||||
| chr3:149138587 | A | C | 3 | a0001c0002t0003g0030 a0001c0002t0016g0030 a0001c0002t0016g0178 |
3 | HG01070.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.218-1417A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138587 | |||||||
| chr3:149138765 | A | G | 2 | a0001c0002t0001g0282 a0001c0002t0003g0283 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-1239A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138765 | |||||||
| chr3:149138954 | A | C | 15 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(12): Show |
18 | HG01167.hp1 HG01192.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-1050A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149138954 | |||||||
| chr3:149139147 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0011g0284 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-857T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139147 | |||||||
| chr3:149139383 | G | A | 1 | a0001c0003t0001g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218-621G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139383 | |||||||
| chr3:149139446 | G | A | 4 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-558G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139446 | |||||||
| chr3:149139464 | C | T | 57 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0038 others(54): Show |
66 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.218-540C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139464 | |||||||
| chr3:149139494 | T | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(60): Show |
80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.218-510T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139494 | |||||||
| chr3:149139535 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0115 others(4): Show |
9 | HG00140.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.218-469A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139535 | |||||||
| chr3:149139648 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.218-356T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139648 | |||||||
| chr3:149139903 | C | T | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-101C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139903 | |||||||
| chr3:149139927 | A | C | 9 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(6): Show |
12 | HG01516.hp1 HG02055.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-77A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 1/16 | chr3 | 149139927 | |||||||
| chr3:149140675 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.712+177T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/16 | chr3 | 149140675 | |||||||
| chr3:149140775 | A | C | 15 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.713-242A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/16 | chr3 | 149140775 | |||||||
| chr3:149140912 | G | A | 2 | a0001c0003t0022g0276 a0001c0003t0022g0277 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.713-105G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 2/16 | chr3 | 149140912 | |||||||
| chr3:149141200 | C | CT | 9 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0001t0002g0233 others(6): Show |
9 | HG02027.hp1 HG02155.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.884+25dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 149141200 | ||||||
| chr3:149141200 | C | CTT | 26 | a0001c0002t0003g0283 a0001c0002t0029g0067 a0001c0002t0032g0128 others(23): Show |
30 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.884+24_884+25dupTT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 149141200 | ||||||
| chr3:149141200 | C | CTTT | 40 | a0001c0001t0001g0068 a0001c0002t0001g0049 a0001c0002t0001g0055 others(37): Show |
43 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.884+23_884+25dupTT others(1): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 149141200 | ||||||
| chr3:149141200 | C | CTTTT | 51 | a0001c0001t0001g0127 a0001c0001t0002g0085 a0001c0002t0006g0046 others(48): Show |
58 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.884+22_884+25dupTT others(2): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 149141200 | ||||||
| chr3:149141200 | C | CTTTTT | 64 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(61): Show |
81 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.884+21_884+25dupTT others(3): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 149141200 | ||||||
| chr3:149141215 | C | A | 1 | a0001c0004t0002g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.884+27C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 3/16 | chr3 | 149141215 | |||||||
| chr3:149141387 | A | G | 6 | a0001c0002t0030g0145 a0001c0006t0001g0143 a0001c0006t0001g0144 others(3): Show |
6 | HG02273.hp1 HG02683.hp2 HG02698.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.970+7A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141387 | |||||||
| chr3:149141403 | G | A | 1 | a0001c0004t0002g0086 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.970+23G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141403 | |||||||
| chr3:149141404 | C | T | 1 | a0001c0005t0023g0074 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.970+24C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141404 | |||||||
| chr3:149141519 | G | GT | 16 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.970+150dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149141519 | ||||||
| chr3:149141531 | G | GT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
11 | HG00438.hp2 HG00738.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.970+172dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149141531 | ||||||
| chr3:149141531 | G | T | 6 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0003g0177 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.970+151G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141531 | |||||||
| chr3:149141531 | GT | G | 83 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(80): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.970+172delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149141531 | ||||||
| chr3:149141531 | GTT | G | 24 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(21): Show |
28 | HG01167.hp1 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.970+171_970+172del others(2): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149141531 | ||||||
| chr3:149141532 | T | G | 5 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0011g0284 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+152T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141532 | |||||||
| chr3:149141538 | T | G | 5 | a0001c0001t0001g0152 a0001c0002t0001g0140 a0001c0002t0003g0139 others(2): Show |
5 | NA18952.hp1 NA19064.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+158T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141538 | |||||||
| chr3:149141539 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0187 a0001c0002t0008g0185 others(1): Show |
6 | HG00099.hp2 HG00673.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.970+159T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141539 | |||||||
| chr3:149141541 | T | G | 59 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0038 others(56): Show |
68 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.970+161T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141541 | |||||||
| chr3:149141542 | T | G | 103 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(100): Show |
121 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.970+162T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141542 | |||||||
| chr3:149141543 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.970+163T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141543 | |||||||
| chr3:149141544 | T | G | 3 | a0001c0002t0003g0030 a0001c0002t0016g0030 a0001c0002t0016g0178 |
3 | HG01070.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.970+164T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141544 | |||||||
| chr3:149141545 | T | G | 15 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(12): Show |
18 | HG01167.hp1 HG01192.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.970+165T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141545 | |||||||
| chr3:149141659 | G | A | 9 | a0001c0003t0001g0018 a0001c0003t0001g0296 a0001c0003t0003g0294 others(6): Show |
12 | HG01516.hp1 HG02055.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.970+279G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141659 | |||||||
| chr3:149141831 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.970+451G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141831 | |||||||
| chr3:149141946 | G | T | 1 | a0001c0005t0003g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.970+566G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141946 | |||||||
| chr3:149141975 | C | T | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.970+595C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141975 | |||||||
| chr3:149141976 | G | A | 3 | a0001c0002t0001g0282 a0001c0002t0003g0283 a0001c0002t0032g0128 |
3 | HG02145.hp1 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.970+596G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149141976 | |||||||
| chr3:149142007 | C | A | 1 | a0001c0004t0002g0086 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.970+627C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142007 | |||||||
| chr3:149142077 | C | T | 3 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 |
3 | HG02109.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.970+697C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142077 | |||||||
| chr3:149142416 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.970+1036C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142416 | |||||||
| chr3:149142425 | G | T | 1 | a0001c0003t0001g0014 | 3 | HG03490.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.970+1045G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142425 | |||||||
| chr3:149142559 | A | G | 2 | a0001c0002t0001g0282 a0001c0002t0032g0128 |
2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.970+1179A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142559 | |||||||
| chr3:149142654 | ATTTT | A | 60 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0038 others(57): Show |
69 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.970+1280_970+1283d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149142654 | ||||||
| chr3:149142753 | G | A | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.970+1373G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142753 | |||||||
| chr3:149142801 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.970+1421T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142801 | |||||||
| chr3:149142949 | T | C | 1 | a0001c0005t0015g0041 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.970+1569T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142949 | |||||||
| chr3:149142962 | G | A | 4 | a0001c0003t0001g0004 a0001c0003t0001g0250 a0001c0003t0004g0004 others(1): Show |
9 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.970+1582G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142962 | |||||||
| chr3:149142980 | T | C | 1 | a0001c0002t0011g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.970+1600T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149142980 | |||||||
| chr3:149143206 | G | T | 114 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0001g0049 others(111): Show |
129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.970+1826G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143206 | |||||||
| chr3:149143320 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.970+1940G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143320 | |||||||
| chr3:149143384 | A | G | 187 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(184): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.971-1970A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143384 | |||||||
| chr3:149143446 | G | C | 4 | a0001c0005t0018g0072 a0001c0005t0023g0074 a0001c0005t0026g0071 others(1): Show |
4 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-1908G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143446 | |||||||
| chr3:149143497 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.971-1857C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143497 | |||||||
| chr3:149143520 | T | G | 2 | a0001c0004t0002g0088 a0001c0004t0002g0089 |
2 | NA18954.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.971-1834T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143520 | |||||||
| chr3:149143650 | A | T | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.971-1704A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143650 | |||||||
| chr3:149143745 | A | G | 7 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 others(4): Show |
7 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.971-1609A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143745 | |||||||
| chr3:149143791 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.971-1563C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143791 | |||||||
| chr3:149143798 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.971-1556A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143798 | |||||||
| chr3:149143908 | A | C | 1 | a0001c0002t0027g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.971-1446A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143908 | |||||||
| chr3:149143944 | A | G | 15 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.971-1410A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149143944 | |||||||
| chr3:149144099 | G | A | 9 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0006g0148 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.971-1255G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144099 | |||||||
| chr3:149144105 | G | A | 1 | a0001c0002t0032g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.971-1249G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144105 | |||||||
| chr3:149144147 | T | C | 29 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(26): Show |
30 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.971-1207T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144147 | |||||||
| chr3:149144173 | G | A | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.971-1181G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144173 | |||||||
| chr3:149144182 | C | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(62): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.971-1172C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144182 | |||||||
| chr3:149144204 | G | T | 14 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(11): Show |
15 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.971-1150G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144204 | |||||||
| chr3:149144214 | G | GA | 142 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(139): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.971-1121dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149144214 | ||||||
| chr3:149144214 | G | GAA | 11 | a0001c0001t0003g0075 a0001c0001t0008g0084 a0001c0003t0001g0252 others(8): Show |
11 | HG01952.hp1 HG02738.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.971-1122_971-1121d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149144214 | ||||||
| chr3:149144214 | GAAAAA | G | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.971-1125_971-1121d others(7): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 149144214 | ||||||
| chr3:149144239 | C | A | 5 | a0001c0003t0001g0242 a0001c0003t0002g0241 a0001c0003t0004g0243 others(2): Show |
6 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.971-1115C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144239 | |||||||
| chr3:149144244 | A | T | 14 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(11): Show |
15 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.971-1110A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144244 | |||||||
| chr3:149144255 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0041g0111 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.971-1099C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144255 | |||||||
| chr3:149144256 | G | A | 63 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.971-1098G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144256 | |||||||
| chr3:149144332 | G | A | 1 | a0001c0003t0001g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.971-1022G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144332 | |||||||
| chr3:149144567 | C | T | 1 | a0001c0002t0032g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.971-787C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144567 | |||||||
| chr3:149144643 | G | T | 14 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(11): Show |
15 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.971-711G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144643 | |||||||
| chr3:149144694 | T | G | 20 | a0001c0005t0003g0285 a0001c0005t0005g0137 a0001c0005t0006g0024 others(17): Show |
21 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.971-660T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144694 | |||||||
| chr3:149144699 | T | C | 1 | a0001c0003t0004g0236 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.971-655T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144699 | |||||||
| chr3:149144711 | A | G | 2 | a0001c0004t0002g0108 a0001c0004t0004g0109 |
2 | NA18960.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.971-643A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144711 | |||||||
| chr3:149144750 | C | T | 20 | a0001c0005t0003g0285 a0001c0005t0005g0137 a0001c0005t0006g0024 others(17): Show |
21 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.971-604C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144750 | |||||||
| chr3:149144751 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.971-603G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144751 | |||||||
| chr3:149144795 | C | A | 8 | a0001c0003t0009g0039 a0001c0003t0009g0228 a0001c0003t0009g0239 others(5): Show |
8 | HG00597.hp1 HG02056.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.971-559C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144795 | |||||||
| chr3:149144818 | G | A | 20 | a0001c0005t0003g0285 a0001c0005t0005g0137 a0001c0005t0006g0024 others(17): Show |
21 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.971-536G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144818 | |||||||
| chr3:149144836 | A | G | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.971-518A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144836 | |||||||
| chr3:149144949 | A | T | 20 | a0001c0005t0003g0285 a0001c0005t0005g0137 a0001c0005t0006g0024 others(17): Show |
21 | HG01167.hp1 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.971-405A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149144949 | |||||||
| chr3:149145069 | C | A | 82 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(79): Show |
94 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.971-285C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149145069 | |||||||
| chr3:149145311 | T | C | 15 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.971-43T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 4/16 | chr3 | 149145311 | |||||||
| chr3:149145608 | T | G | 92 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(89): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1163+62T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149145608 | |||||||
| chr3:149145711 | A | G | 1 | a0001c0002t0003g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1163+165A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149145711 | |||||||
| chr3:149145797 | A | G | 92 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(89): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1163+251A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149145797 | |||||||
| chr3:149145804 | A | C | 92 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(89): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1163+258A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149145804 | |||||||
| chr3:149145985 | T | C | 107 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(104): Show |
122 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1163+439T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149145985 | |||||||
| chr3:149146030 | G | C | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163+484G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146030 | |||||||
| chr3:149146044 | C | G | 3 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 |
3 | HG02109.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1163+498C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146044 | |||||||
| chr3:149146214 | C | T | 1 | a0001c0001t0003g0036 | 2 | NA18970.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1163+668C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146214 | |||||||
| chr3:149146395 | T | C | 1 | a0001c0002t0006g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1163+849T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146395 | |||||||
| chr3:149146435 | A | G | 3 | a0001c0005t0018g0072 a0001c0005t0023g0074 a0006c0020t0024g0073 |
3 | HG01167.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1163+889A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146435 | |||||||
| chr3:149146468 | T | C | 1 | a0001c0006t0011g0141 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1163+922T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146468 | |||||||
| chr3:149146493 | G | T | 1 | a0001c0002t0001g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1163+947G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146493 | |||||||
| chr3:149146532 | G | A | 1 | a0001c0002t0006g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1163+986G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146532 | |||||||
| chr3:149146573 | C | T | 10 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(7): Show |
10 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163+1027C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146573 | |||||||
| chr3:149146586 | G | T | 92 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(89): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1163+1040G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146586 | |||||||
| chr3:149146598 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0234 |
2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1163+1052C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146598 | |||||||
| chr3:149146743 | G | A | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163+1197G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146743 | |||||||
| chr3:149146756 | C | T | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163+1210C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146756 | |||||||
| chr3:149146852 | C | G | 1 | a0001c0003t0004g0243 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1163+1306C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146852 | |||||||
| chr3:149146857 | G | T | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163+1311G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149146857 | |||||||
| chr3:149147020 | G | A | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163+1474G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147020 | |||||||
| chr3:149147064 | C | G | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163+1518C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147064 | |||||||
| chr3:149147091 | A | G | 3 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 |
3 | HG02109.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1163+1545A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147091 | |||||||
| chr3:149147120 | T | G | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163+1574T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147120 | |||||||
| chr3:149147124 | G | A | 2 | a0001c0003t0002g0255 a0001c0003t0002g0256 |
2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1163+1578G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147124 | |||||||
| chr3:149147132 | G | T | 1 | a0001c0005t0019g0135 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1163+1586G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147132 | |||||||
| chr3:149147325 | C | T | 1 | a0001c0002t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1163+1779C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147325 | |||||||
| chr3:149147362 | A | G | 1 | a0001c0003t0001g0271 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1163+1816A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147362 | |||||||
| chr3:149147404 | A | G | 3 | a0001c0001t0001g0127 a0001c0002t0004g0130 a0001c0002t0012g0129 |
3 | HG02109.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1163+1858A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147404 | |||||||
| chr3:149147698 | G | T | 1 | a0001c0002t0027g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1163+2152G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147698 | |||||||
| chr3:149147741 | C | T | 169 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(166): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1163+2195C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147741 | |||||||
| chr3:149147892 | C | T | 73 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(70): Show |
87 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1163+2346C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147892 | |||||||
| chr3:149147932 | G | A | 1 | a0001c0002t0008g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1163+2386G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147932 | |||||||
| chr3:149147961 | C | T | 1 | a0001c0002t0010g0045 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1163+2415C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147961 | |||||||
| chr3:149147978 | C | T | 1 | a0001c0002t0029g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1163+2432C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147978 | |||||||
| chr3:149147989 | A | G | 191 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(188): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1163+2443A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149147989 | |||||||
| chr3:149148000 | C | T | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163+2454C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148000 | |||||||
| chr3:149148023 | G | C | 1 | a0001c0002t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1163+2477G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148023 | |||||||
| chr3:149148069 | C | A | 83 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(80): Show |
98 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1163+2523C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148069 | |||||||
| chr3:149148169 | G | A | 3 | a0002c0007t0003g0020 a0002c0007t0005g0079 a0002c0007t0005g0238 |
4 | HG02717.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164-2430G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148169 | |||||||
| chr3:149148174 | A | G | 1 | a0001c0004t0002g0107 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1164-2425A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148174 | |||||||
| chr3:149148281 | G | A | 1 | a0001c0003t0007g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1164-2318G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148281 | |||||||
| chr3:149148372 | A | G | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1164-2227A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148372 | |||||||
| chr3:149148399 | C | CT | 13 | a0001c0001t0001g0133 a0001c0001t0001g0187 a0001c0001t0004g0171 others(10): Show |
13 | HG00673.hp2 HG01167.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164-2179dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148399 | ||||||
| chr3:149148399 | C | CTT | 35 | a0001c0001t0001g0068 a0001c0002t0008g0060 a0001c0003t0001g0018 others(32): Show |
39 | HG01069.hp1 HG01243.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.1164-2180_1164-217 others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148399 | ||||||
| chr3:149148399 | C | CTTT | 63 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1164-2181_1164-217 others(7): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148399 | ||||||
| chr3:149148399 | CT | C | 14 | a0001c0001t0001g0127 a0001c0001t0001g0192 a0001c0001t0003g0066 others(11): Show |
14 | HG00323.hp1 HG01069.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1164-2179delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148399 | ||||||
| chr3:149148399 | CTT | C | 63 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(60): Show |
81 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1164-2180_1164-217 others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148399 | ||||||
| chr3:149148399 | CTTT | C | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164-2181_1164-217 others(7): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148399 | ||||||
| chr3:149148434 | G | A | 36 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(33): Show |
45 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1164-2165G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148434 | |||||||
| chr3:149148464 | G | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(74): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1164-2135G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148464 | |||||||
| chr3:149148480 | G | A | 6 | a0001c0005t0003g0285 a0001c0005t0010g0288 a0001c0005t0012g0010 others(3): Show |
7 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164-2119G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148480 | |||||||
| chr3:149148552 | A | G | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1164-2047A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148552 | |||||||
| chr3:149148594 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(73): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-2005G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148594 | |||||||
| chr3:149148647 | C | T | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1164-1952C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148647 | |||||||
| chr3:149148713 | T | G | 79 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0001g0049 others(76): Show |
94 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-1886T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148713 | |||||||
| chr3:149148716 | T | G | 222 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0032 others(219): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1164-1883T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148716 | |||||||
| chr3:149148719 | G | A | 2 | a0001c0002t0003g0283 a0001c0002t0032g0128 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1164-1880G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148719 | |||||||
| chr3:149148798 | C | T | 1 | a0001c0002t0004g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1164-1801C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148798 | |||||||
| chr3:149148883 | C | T | 1 | a0001c0004t0004g0105 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1164-1716C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148883 | |||||||
| chr3:149148885 | T | G | 1 | a0001c0003t0004g0243 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1164-1714T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148885 | |||||||
| chr3:149148888 | G | A | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1164-1711G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148888 | |||||||
| chr3:149148898 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1164-1701G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148898 | |||||||
| chr3:149148921 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(187): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1164-1678C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148921 | |||||||
| chr3:149148949 | C | CT | 11 | a0001c0001t0001g0133 a0001c0001t0001g0222 a0001c0001t0001g0223 others(8): Show |
11 | HG01175.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1164-1628dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148949 | ||||||
| chr3:149148949 | CT | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(62): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1164-1628delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148949 | ||||||
| chr3:149148949 | CTTTTT | C | 92 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(89): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1164-1632_1164-162 others(9): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149148949 | ||||||
| chr3:149148995 | C | T | 6 | a0001c0002t0006g0148 a0001c0002t0006g0149 a0001c0002t0006g0150 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164-1604C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149148995 | |||||||
| chr3:149149047 | G | A | 45 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(42): Show |
54 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1164-1552G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149047 | |||||||
| chr3:149149098 | C | T | 93 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1164-1501C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149098 | |||||||
| chr3:149149099 | G | A | 61 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0014 others(58): Show |
72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1164-1500G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149099 | |||||||
| chr3:149149111 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(73): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-1488G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149111 | |||||||
| chr3:149149120 | A | AT | 6 | a0001c0001t0001g0221 a0001c0001t0003g0066 a0001c0002t0027g0121 others(3): Show |
6 | HG00597.hp2 HG02602.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164-1463dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149149120 | ||||||
| chr3:149149161 | C | T | 1 | a0001c0002t0008g0186 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1164-1438C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149161 | |||||||
| chr3:149149255 | G | A | 78 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(75): Show |
97 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1164-1344G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149255 | |||||||
| chr3:149149319 | C | T | 1 | a0001c0004t0002g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1164-1280C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149319 | |||||||
| chr3:149149339 | G | A | 73 | a0001c0001t0001g0068 a0001c0003t0001g0004 a0001c0003t0001g0005 others(70): Show |
87 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164-1260G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149339 | |||||||
| chr3:149149354 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(73): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-1245G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149354 | |||||||
| chr3:149149383 | C | T | 1 | a0001c0004t0002g0089 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1164-1216C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149383 | |||||||
| chr3:149149547 | C | T | 2 | a0001c0001t0003g0066 a0001c0002t0035g0065 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1164-1052C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149547 | |||||||
| chr3:149149575 | A | T | 1 | a0001c0002t0008g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1164-1024A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149575 | |||||||
| chr3:149149644 | C | CT | 76 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(73): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-946dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149149644 | ||||||
| chr3:149149644 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0180 a0001c0001t0001g0220 others(2): Show |
6 | NA18948.hp2 NA18949.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164-955C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149644 | |||||||
| chr3:149149646 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0230 a0001c0001t0001g0232 others(2): Show |
6 | HG00738.hp1 HG01106.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164-953T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149646 | |||||||
| chr3:149149803 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(73): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-796G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149803 | |||||||
| chr3:149149812 | G | A | 10 | a0001c0005t0003g0285 a0001c0005t0006g0290 a0001c0005t0010g0288 others(7): Show |
11 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1164-787G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149812 | |||||||
| chr3:149149858 | A | G | 1 | a0001c0003t0004g0236 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1164-741A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149149858 | |||||||
| chr3:149150053 | G | T | 1 | a0001c0003t0002g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1164-546G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150053 | |||||||
| chr3:149150164 | T | A | 6 | a0001c0001t0001g0188 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG01109.hp1 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164-435T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150164 | |||||||
| chr3:149150201 | C | A | 164 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(161): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1164-398C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150201 | |||||||
| chr3:149150223 | A | G | 11 | a0001c0002t0029g0067 a0001c0005t0003g0285 a0001c0005t0006g0290 others(8): Show |
12 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1164-376A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150223 | |||||||
| chr3:149150266 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0180 |
3 | NA18949.hp2 NA18973.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1164-333A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150266 | |||||||
| chr3:149150374 | C | G | 76 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(73): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1164-225C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150374 | |||||||
| chr3:149150407 | A | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(70): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1164-192A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150407 | |||||||
| chr3:149150413 | T | C | 1 | a0001c0003t0001g0274 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1164-186T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150413 | |||||||
| chr3:149150460 | A | C | 239 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(236): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1164-139A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150460 | |||||||
| chr3:149150492 | G | A | 5 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(2): Show |
5 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164-107G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150492 | |||||||
| chr3:149150505 | GC | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(70): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1164-91delC | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 149150505 | ||||||
| chr3:149150574 | C | T | 66 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(63): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1164-25C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 5/16 | chr3 | 149150574 | |||||||
| chr3:149150739 | C | G | 12 | a0001c0002t0003g0283 a0001c0002t0032g0128 a0001c0005t0003g0285 others(9): Show |
13 | HG01243.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1245+59C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149150739 | |||||||
| chr3:149150767 | A | G | 1 | a0001c0004t0002g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1245+87A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149150767 | |||||||
| chr3:149150792 | T | C | 2 | a0001c0003t0002g0280 a0001c0003t0002g0281 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1245+112T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149150792 | |||||||
| chr3:149150902 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1245+222G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149150902 | |||||||
| chr3:149150911 | C | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(70): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1245+231C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149150911 | |||||||
| chr3:149150987 | T | C | 1 | a0001c0002t0027g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1245+307T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149150987 | |||||||
| chr3:149151004 | G | A | 73 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(70): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1245+324G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151004 | |||||||
| chr3:149151012 | CT | C | 73 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(70): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1245+336delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151012 | ||||||
| chr3:149151062 | C | T | 2 | a0001c0002t0003g0283 a0001c0002t0032g0128 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1245+382C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151062 | |||||||
| chr3:149151183 | G | GTAT | 58 | a0001c0002t0008g0185 a0001c0003t0001g0005 a0001c0003t0001g0014 others(55): Show |
64 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1245+523_1245+525d others(5): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151183 | ||||||
| chr3:149151183 | G | GTATTAT | 4 | a0001c0003t0001g0004 a0001c0003t0001g0250 a0001c0003t0004g0004 others(1): Show |
9 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1245+520_1245+525d others(8): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151183 | ||||||
| chr3:149151197 | A | AT | 3 | a0001c0004t0004g0122 a0001c0004t0004g0124 a0001c0004t0004g0126 |
3 | HG00323.hp2 HG01255.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1245+519dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151197 | ||||||
| chr3:149151200 | A | AT | 58 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(55): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1245+522dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151200 | ||||||
| chr3:149151200 | A | T | 5 | a0001c0004t0004g0122 a0001c0004t0004g0124 a0001c0004t0004g0126 others(2): Show |
5 | HG00323.hp2 HG01255.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245+520A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151200 | |||||||
| chr3:149151203 | A | ATTAT | 6 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+525_1245+526i others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151203 | ||||||
| chr3:149151203 | A | T | 80 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0031 others(77): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1245+523A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151203 | |||||||
| chr3:149151206 | T | A | 73 | a0001c0001t0001g0068 a0001c0001t0001g0133 a0001c0002t0027g0121 others(70): Show |
87 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1245+526T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151206 | |||||||
| chr3:149151237 | C | T | 3 | a0001c0002t0001g0282 a0001c0003t0003g0248 a0001c0003t0004g0249 |
3 | HG01891.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1245+557C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151237 | |||||||
| chr3:149151326 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1245+646C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151326 | |||||||
| chr3:149151422 | A | G | 7 | a0001c0002t0001g0282 a0001c0002t0006g0046 a0001c0002t0010g0043 others(4): Show |
7 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245+742A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151422 | |||||||
| chr3:149151433 | G | A | 89 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0003g0066 others(86): Show |
103 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1245+753G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151433 | |||||||
| chr3:149151522 | G | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(187): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1245+842G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151522 | |||||||
| chr3:149151537 | A | G | 2 | a0001c0005t0006g0024 a0001c0005t0033g0024 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1245+857A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151537 | |||||||
| chr3:149151587 | T | TA | 55 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0034 others(52): Show |
72 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1245+936dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | T | TAA | 9 | a0001c0001t0001g0127 a0001c0001t0001g0229 a0001c0001t0004g0026 others(6): Show |
11 | HG00558.hp1 HG02165.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1245+935_1245+936d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | T | TAAA | 6 | a0001c0002t0001g0282 a0001c0002t0009g0155 a0001c0002t0010g0043 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+934_1245+936d others(5): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | T | TAAAAAAA | 6 | a0001c0002t0002g0058 a0001c0002t0008g0064 a0001c0002t0017g0057 others(3): Show |
6 | HG03139.hp1 HG03453.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+930_1245+936d others(9): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | T | TAAAAAAA others(1): Show |
8 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0008g0050 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1245+929_1245+936d others(10): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | T | TAAAAAAA others(3): Show |
1 | a0001c0002t0008g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1245+927_1245+936d others(12): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | TA | T | 11 | a0001c0001t0001g0131 a0001c0001t0001g0188 a0001c0001t0003g0066 others(8): Show |
11 | HG00558.hp2 HG01074.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1245+936delA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | TAA | T | 6 | a0001c0005t0003g0285 a0001c0005t0010g0288 a0001c0005t0012g0010 others(3): Show |
7 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1245+935_1245+936d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151587 | TAAAAAAA others(3): Show |
T | 3 | a0002c0007t0003g0020 a0002c0007t0005g0079 a0002c0007t0005g0238 |
4 | HG02717.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245+927_1245+936d others(12): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 149151587 | ||||||
| chr3:149151588 | A | T | 2 | a0001c0002t0003g0283 a0001c0002t0032g0128 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1245+908A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151588 | |||||||
| chr3:149151590 | A | T | 6 | a0001c0005t0003g0285 a0001c0005t0010g0288 a0001c0005t0012g0010 others(3): Show |
7 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1245+910A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151590 | |||||||
| chr3:149151591 | A | T | 4 | a0001c0005t0006g0290 a0001c0005t0012g0289 a0001c0005t0031g0286 others(1): Show |
4 | HG01433.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245+911A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151591 | |||||||
| chr3:149151613 | AAAAG | A | 7 | a0001c0003t0001g0014 a0001c0003t0002g0256 a0001c0003t0002g0281 others(4): Show |
9 | HG01516.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1245+934_1245+937d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151613 | |||||||
| chr3:149151614 | AAAG | A | 47 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0038 others(44): Show |
55 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1245+935_1245+937d others(5): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151614 | |||||||
| chr3:149151615 | AAG | A | 8 | a0001c0003t0001g0005 a0001c0003t0001g0242 a0001c0003t0001g0259 others(5): Show |
8 | HG01243.hp1 HG01517.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1245+936_1245+937d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151615 | |||||||
| chr3:149151616 | AG | A | 4 | a0001c0003t0003g0294 a0001c0005t0003g0246 a0001c0005t0015g0041 others(1): Show |
4 | HG02055.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245+937delG | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151616 | |||||||
| chr3:149151617 | G | A | 15 | a0001c0001t0001g0068 a0001c0003t0001g0018 a0001c0003t0001g0296 others(12): Show |
17 | HG01516.hp1 HG02615.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1245+937G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151617 | |||||||
| chr3:149151844 | T | C | 93 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0003g0283 others(90): Show |
108 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1245+1164T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151844 | |||||||
| chr3:149151873 | G | A | 89 | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0002t0003g0283 others(86): Show |
104 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1245+1193G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151873 | |||||||
| chr3:149151892 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1245+1212G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149151892 | |||||||
| chr3:149152045 | G | A | 4 | a0001c0005t0018g0072 a0001c0005t0023g0074 a0001c0005t0026g0071 others(1): Show |
4 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245+1365G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152045 | |||||||
| chr3:149152391 | G | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(85): Show |
106 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1246-1103G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152391 | |||||||
| chr3:149152470 | G | A | 6 | a0001c0002t0002g0163 a0001c0002t0003g0161 a0001c0002t0003g0172 others(3): Show |
6 | HG00280.hp2 HG01123.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1246-1024G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152470 | |||||||
| chr3:149152484 | G | A | 1 | a0001c0002t0006g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1246-1010G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152484 | |||||||
| chr3:149152511 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1246-983C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152511 | |||||||
| chr3:149152572 | C | T | 9 | a0001c0001t0001g0068 a0001c0003t0001g0018 a0001c0003t0001g0296 others(6): Show |
11 | HG01516.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1246-922C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152572 | |||||||
| chr3:149152575 | G | A | 1 | a0001c0002t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1246-919G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152575 | |||||||
| chr3:149152929 | C | T | 1 | a0001c0002t0011g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1246-565C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152929 | |||||||
| chr3:149152962 | T | A | 1 | a0001c0002t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1246-532T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152962 | |||||||
| chr3:149152987 | A | T | 2 | a0001c0003t0002g0280 a0001c0003t0002g0281 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1246-507A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149152987 | |||||||
| chr3:149153024 | C | T | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-470C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149153024 | |||||||
| chr3:149153097 | G | A | 1 | a0001c0004t0002g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1246-397G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149153097 | |||||||
| chr3:149153279 | A | G | 15 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1246-215A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149153279 | |||||||
| chr3:149153337 | C | T | 87 | a0001c0001t0001g0021 a0001c0001t0001g0110 a0001c0001t0003g0066 others(84): Show |
103 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1246-157C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 6/16 | chr3 | 149153337 | |||||||
| chr3:149153689 | G | A | 7 | a0001c0002t0006g0046 a0001c0002t0010g0043 a0001c0002t0010g0044 others(4): Show |
7 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1400+41G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149153689 | |||||||
| chr3:149153745 | A | G | 19 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(16): Show |
19 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1400+97A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149153745 | |||||||
| chr3:149153782 | A | G | 1 | a0001c0004t0002g0086 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1400+134A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149153782 | |||||||
| chr3:149153856 | A | G | 1 | a0001c0002t0032g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1400+208A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149153856 | |||||||
| chr3:149153892 | T | C | 9 | a0001c0005t0003g0285 a0001c0005t0010g0288 a0001c0005t0012g0010 others(6): Show |
10 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1400+244T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149153892 | |||||||
| chr3:149153920 | T | C | 4 | a0001c0003t0007g0293 a0002c0007t0003g0020 a0002c0007t0005g0079 others(1): Show |
5 | HG02717.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+272T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149153920 | |||||||
| chr3:149154082 | A | G | 9 | a0001c0002t0003g0006 a0001c0002t0003g0151 a0001c0002t0003g0168 others(6): Show |
13 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1400+434A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154082 | |||||||
| chr3:149154200 | A | G | 1 | a0001c0003t0001g0296 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1400+552A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154200 | |||||||
| chr3:149154213 | T | C | 161 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0147 others(158): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1400+565T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154213 | |||||||
| chr3:149154223 | T | C | 174 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0031 others(171): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1400+575T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154223 | |||||||
| chr3:149154289 | A | G | 1 | a0001c0002t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1400+641A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154289 | |||||||
| chr3:149154334 | G | A | 110 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0068 others(107): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1400+686G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154334 | |||||||
| chr3:149154595 | A | T | 64 | a0001c0002t0001g0140 a0001c0002t0002g0163 a0001c0002t0002g0219 others(61): Show |
79 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1401-512A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149154595 | |||||||
| chr3:149155004 | T | A | 1 | a0001c0006t0011g0141 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1401-103T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 7/16 | chr3 | 149155004 | |||||||
| chr3:149155463 | G | A | 2 | a0001c0004t0002g0108 a0001c0004t0004g0109 |
2 | NA18960.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1509+248G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149155463 | |||||||
| chr3:149155531 | C | CAAAT | 3 | a0001c0002t0030g0145 a0001c0005t0018g0072 a0001c0005t0023g0074 |
3 | HG01167.hp1 HG01346.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1509+337_1509+340d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 149155531 | ||||||
| chr3:149155576 | C | G | 69 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(66): Show |
84 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1509+361C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149155576 | |||||||
| chr3:149155604 | A | C | 3 | a0001c0002t0011g0284 a0001c0002t0035g0065 a0001c0005t0040g0287 |
3 | HG02257.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1509+389A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149155604 | |||||||
| chr3:149155772 | T | A | 1 | a0001c0003t0020g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1509+557T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149155772 | |||||||
| chr3:149155927 | T | G | 3 | a0001c0002t0011g0284 a0001c0002t0035g0065 a0001c0005t0040g0287 |
3 | HG02257.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1509+712T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149155927 | |||||||
| chr3:149155988 | C | T | 8 | a0001c0002t0012g0129 a0001c0005t0010g0288 a0001c0005t0012g0010 others(5): Show |
9 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+773C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149155988 | |||||||
| chr3:149156162 | A | C | 3 | a0001c0002t0011g0284 a0001c0002t0035g0065 a0001c0005t0040g0287 |
3 | HG02257.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1509+947A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156162 | |||||||
| chr3:149156272 | C | T | 1 | a0001c0018t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1509+1057C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156272 | |||||||
| chr3:149156465 | G | T | 141 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(138): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1510-885G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156465 | |||||||
| chr3:149156551 | G | A | 1 | a0001c0003t0001g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1510-799G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156551 | |||||||
| chr3:149156574 | CT | C | 9 | a0001c0001t0001g0200 a0001c0002t0004g0130 a0001c0002t0010g0043 others(6): Show |
9 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1510-764delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 149156574 | ||||||
| chr3:149156593 | T | A | 1 | a0001c0004t0002g0093 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1510-757T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156593 | |||||||
| chr3:149156773 | A | C | 1 | a0001c0005t0023g0074 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1510-577A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156773 | |||||||
| chr3:149156780 | C | T | 8 | a0001c0002t0012g0129 a0001c0005t0010g0288 a0001c0005t0012g0010 others(5): Show |
9 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510-570C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149156780 | |||||||
| chr3:149157161 | C | T | 2 | a0001c0005t0015g0041 a0001c0005t0036g0292 |
3 | HG02055.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1510-189C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | chr3 | 149157161 | |||||||
| chr3:149157206 | TG | T | 5 | a0001c0002t0030g0145 a0001c0005t0018g0072 a0001c0005t0023g0074 others(2): Show |
5 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-142delG | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 149157206 | ||||||
| chr3:149157838 | T | C | 1 | a0001c0002t0008g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1691+307T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 9/16 | chr3 | 149157838 | |||||||
| chr3:149157896 | C | T | 5 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(2): Show |
5 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1691+365C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 9/16 | chr3 | 149157896 | |||||||
| chr3:149157964 | A | C | 51 | a0001c0004t0001g0012 a0001c0004t0001g0095 a0001c0004t0001g0119 others(48): Show |
66 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1691+433A>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 9/16 | chr3 | 149157964 | |||||||
| chr3:149158313 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1692-353T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 9/16 | chr3 | 149158313 | |||||||
| chr3:149158474 | T | G | 244 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0031 others(241): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1692-192T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 9/16 | chr3 | 149158474 | |||||||
| chr3:149158592 | A | G | 3 | a0001c0002t0011g0284 a0001c0002t0035g0065 a0001c0005t0040g0287 |
3 | HG02257.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1692-74A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 9/16 | chr3 | 149158592 | |||||||
| chr3:149159331 | G | A | 1 | a0001c0004t0004g0105 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1872+485G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159331 | |||||||
| chr3:149159394 | C | T | 1 | a0001c0005t0001g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1872+548C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159394 | |||||||
| chr3:149159415 | T | G | 2 | a0001c0003t0001g0040 a0001c0003t0001g0258 |
3 | NA18992.hp1 NA19002.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1872+569T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159415 | |||||||
| chr3:149159422 | G | A | 47 | a0001c0002t0001g0140 a0001c0002t0002g0163 a0001c0002t0003g0003 others(44): Show |
60 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1872+576G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159422 | |||||||
| chr3:149159486 | C | T | 3 | a0001c0004t0004g0122 a0001c0004t0004g0124 a0001c0004t0004g0126 |
3 | HG00323.hp2 HG01255.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1873-560C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159486 | |||||||
| chr3:149159893 | T | C | 141 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(138): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1873-153T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159893 | |||||||
| chr3:149159909 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1873-137T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 10/16 | chr3 | 149159909 | |||||||
| chr3:149160456 | A | G | 51 | a0001c0004t0001g0012 a0001c0004t0001g0095 a0001c0004t0001g0119 others(48): Show |
66 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2106+177A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149160456 | |||||||
| chr3:149160818 | G | A | 153 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(150): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.2106+539G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149160818 | |||||||
| chr3:149160994 | A | G | 1 | a0001c0003t0001g0271 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2106+715A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149160994 | |||||||
| chr3:149161084 | A | G | 141 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(138): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.2106+805A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161084 | |||||||
| chr3:149161245 | C | G | 1 | a0001c0002t0029g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2107-903C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161245 | |||||||
| chr3:149161316 | T | G | 1 | a0001c0004t0002g0094 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2107-832T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161316 | |||||||
| chr3:149161465 | T | TAAAA | 142 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(139): Show |
172 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.2107-682_2107-679d others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 149161465 | ||||||
| chr3:149161508 | C | CT | 25 | a0001c0001t0001g0116 a0001c0001t0001g0183 a0001c0001t0001g0203 others(22): Show |
30 | HG01081.hp1 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2107-617dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 149161508 | ||||||
| chr3:149161508 | CT | C | 84 | a0001c0001t0001g0115 a0001c0001t0001g0201 a0001c0001t0001g0211 others(81): Show |
100 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2107-617delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 149161508 | ||||||
| chr3:149161508 | CTT | C | 7 | a0001c0002t0010g0045 a0001c0003t0001g0260 a0001c0004t0001g0095 others(4): Show |
7 | HG01884.hp2 HG02896.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2107-618_2107-617d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 149161508 | ||||||
| chr3:149161509 | T | C | 4 | a0001c0002t0030g0145 a0001c0005t0018g0072 a0001c0005t0023g0074 others(1): Show |
4 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107-639T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161509 | |||||||
| chr3:149161513 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2107-635T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161513 | |||||||
| chr3:149161517 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2107-631T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161517 | |||||||
| chr3:149161540 | C | T | 1 | a0001c0003t0007g0295 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2107-608C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161540 | |||||||
| chr3:149161705 | T | G | 5 | a0001c0002t0030g0145 a0001c0005t0018g0072 a0001c0005t0023g0074 others(2): Show |
5 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2107-443T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161705 | |||||||
| chr3:149161712 | GT | G | 5 | a0001c0006t0001g0143 a0001c0006t0001g0144 a0001c0006t0011g0141 others(2): Show |
5 | HG02273.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-434delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 149161712 | ||||||
| chr3:149161815 | G | A | 3 | a0001c0002t0003g0168 a0001c0002t0003g0169 a0001c0002t0003g0170 |
3 | HG02630.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2107-333G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161815 | |||||||
| chr3:149161972 | A | G | 5 | a0001c0003t0001g0242 a0001c0003t0001g0244 a0001c0003t0002g0241 others(2): Show |
6 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107-176A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149161972 | |||||||
| chr3:149162091 | A | G | 142 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(139): Show |
172 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.2107-57A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149162091 | |||||||
| chr3:149162096 | A | G | 58 | a0001c0002t0001g0140 a0001c0002t0002g0163 a0001c0002t0002g0219 others(55): Show |
73 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2107-52A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 11/16 | chr3 | 149162096 | |||||||
| chr3:149162396 | C | A | 5 | a0001c0002t0030g0145 a0001c0005t0018g0072 a0001c0005t0023g0074 others(2): Show |
5 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2292+63C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 12/16 | chr3 | 149162396 | |||||||
| chr3:149162442 | CAG | C | 56 | a0001c0002t0001g0140 a0001c0002t0002g0163 a0001c0002t0002g0219 others(53): Show |
71 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.2292+111_2292+112d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 149162442 | ||||||
| chr3:149162621 | C | T | 1 | a0001c0003t0001g0273 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2293-69C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 12/16 | chr3 | 149162621 | |||||||
| chr3:149162650 | A | G | 1 | a0001c0002t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2293-40A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 12/16 | chr3 | 149162650 | |||||||
| chr3:149162883 | G | A | 1 | a0001c0003t0009g0254 | 1 | NA18942.hp2 | splice_region_variant&intron_variant | LOW | c.2481+5G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 13/16 | chr3 | 149162883 | |||||||
| chr3:149163082 | T | C | 1 | a0001c0002t0011g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2481+204T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 13/16 | chr3 | 149163082 | |||||||
| chr3:149163299 | C | T | 1 | a0001c0005t0006g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2481+421C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 13/16 | chr3 | 149163299 | |||||||
| chr3:149163303 | C | G | 2 | a0001c0005t0015g0041 a0001c0005t0036g0292 |
3 | HG02055.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2481+425C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 13/16 | chr3 | 149163303 | |||||||
| chr3:149163339 | G | A | 45 | a0001c0002t0002g0163 a0001c0002t0003g0003 a0001c0002t0003g0006 others(42): Show |
58 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.2481+461G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 13/16 | chr3 | 149163339 | |||||||
| chr3:149163813 | T | G | 6 | a0001c0005t0005g0137 a0001c0005t0006g0024 a0001c0005t0006g0136 others(3): Show |
6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-29T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 13/16 | chr3 | 149163813 | |||||||
| chr3:149164153 | G | T | 3 | a0001c0002t0011g0284 a0001c0002t0035g0065 a0001c0005t0040g0287 |
3 | HG02257.hp1 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2589+204G>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149164153 | |||||||
| chr3:149164259 | A | G | 1 | a0001c0002t0029g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2589+310A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149164259 | |||||||
| chr3:149164697 | G | A | 1 | a0001c0004t0002g0097 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2589+748G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149164697 | |||||||
| chr3:149164773 | C | T | 1 | a0001c0002t0004g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2589+824C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149164773 | |||||||
| chr3:149164783 | G | A | 1 | a0001c0005t0026g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2589+834G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149164783 | |||||||
| chr3:149164913 | C | T | 1 | a0001c0002t0004g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2589+964C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149164913 | |||||||
| chr3:149165379 | A | G | 1 | a0001c0003t0001g0266 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2589+1430A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149165379 | |||||||
| chr3:149165484 | A | AT | 142 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(139): Show |
172 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.2590-1539dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 149165484 | ||||||
| chr3:149165509 | C | T | 6 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2590-1525C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149165509 | |||||||
| chr3:149165721 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0180 a0001c0001t0001g0220 others(2): Show |
6 | NA18948.hp2 NA18949.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2590-1313C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149165721 | |||||||
| chr3:149165762 | C | T | 2 | a0001c0002t0003g0156 a0001c0005t0003g0246 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2590-1272C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149165762 | |||||||
| chr3:149165880 | A | G | 1 | a0001c0002t0032g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2590-1154A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149165880 | |||||||
| chr3:149166092 | A | G | 1 | a0001c0012t0002g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2590-942A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166092 | |||||||
| chr3:149166411 | C | G | 1 | a0001c0003t0001g0265 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2590-623C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166411 | |||||||
| chr3:149166684 | G | A | 136 | a0001c0002t0001g0049 a0001c0002t0001g0055 a0001c0002t0001g0056 others(133): Show |
166 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2590-350G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166684 | |||||||
| chr3:149166692 | T | C | 1 | a0001c0002t0027g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2590-342T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166692 | |||||||
| chr3:149166734 | T | A | 1 | a0001c0005t0040g0287 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2590-300T>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166734 | |||||||
| chr3:149166759 | A | G | 5 | a0001c0002t0030g0145 a0001c0005t0018g0072 a0001c0005t0023g0074 others(2): Show |
5 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2590-275A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166759 | |||||||
| chr3:149166769 | A | G | 4 | a0001c0003t0001g0154 a0001c0003t0001g0259 a0001c0003t0001g0264 others(1): Show |
4 | NA18963.hp2 NA18980.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2590-265A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 14/16 | chr3 | 149166769 | |||||||
| chr3:149167279 | G | A | 47 | a0001c0002t0002g0163 a0001c0002t0003g0003 a0001c0002t0003g0006 others(44): Show |
60 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2796+39G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 15/16 | chr3 | 149167279 | |||||||
| chr3:149167290 | C | T | 156 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0113 others(153): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2796+50C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 15/16 | chr3 | 149167290 | |||||||
| chr3:149167441 | TATC | T | 56 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(53): Show |
71 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.2796+207_2796+209d others(5): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 149167441 | ||||||
| chr3:149167574 | A | T | 1 | a0001c0002t0003g0169 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2797-319A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 15/16 | chr3 | 149167574 | |||||||
| chr3:149167992 | A | AT | 143 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(140): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.2887+19dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149167992 | ||||||
| chr3:149168064 | G | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(320): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.2887+81G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168064 | |||||||
| chr3:149168230 | A | G | 4 | a0001c0002t0002g0219 a0001c0002t0004g0195 a0001c0003t0002g0280 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2887+247A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168230 | |||||||
| chr3:149168246 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2887+263A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168246 | |||||||
| chr3:149168265 | A | G | 2 | a0001c0002t0003g0162 a0001c0002t0003g0173 |
2 | HG00558.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2887+282A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168265 | |||||||
| chr3:149168403 | T | C | 1 | a0001c0004t0002g0094 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2887+420T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168403 | |||||||
| chr3:149168502 | T | C | 3 | a0001c0001t0004g0026 a0001c0001t0004g0171 a0001c0003t0004g0249 |
4 | HG02257.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2887+519T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168502 | |||||||
| chr3:149168536 | C | T | 54 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(51): Show |
67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.2887+553C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168536 | |||||||
| chr3:149168602 | GTT | G | 4 | a0001c0002t0010g0043 a0001c0002t0010g0045 a0001c0002t0010g0048 others(1): Show |
4 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2887+622_2887+623d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149168602 | ||||||
| chr3:149168661 | A | G | 1 | a0001c0003t0001g0014 | 3 | HG03490.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2887+678A>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168661 | |||||||
| chr3:149168727 | A | T | 4 | a0001c0002t0030g0145 a0001c0005t0023g0074 a0001c0005t0026g0071 others(1): Show |
4 | HG01346.hp2 HG01358.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2887+744A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149168727 | |||||||
| chr3:149168906 | CATT | C | 2 | a0001c0002t0009g0029 a0001c0002t0009g0160 |
3 | HG00323.hp1 HG01081.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2887+926_2887+928d others(5): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149168906 | ||||||
| chr3:149169038 | C | CGTGT | 11 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(8): Show |
11 | HG00738.hp2 HG01346.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.2887+1072_2887+107 others(8): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149169038 | ||||||
| chr3:149169038 | C | CGTGTGTG others(1): Show |
8 | a0001c0002t0012g0129 a0001c0005t0010g0288 a0001c0005t0012g0010 others(5): Show |
9 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2887+1068_2887+107 others(12): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149169038 | ||||||
| chr3:149169038 | C | CGTGTGTG others(3): Show |
2 | a0001c0002t0035g0065 a0001c0019t0014g0297 |
2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2887+1066_2887+107 others(14): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149169038 | ||||||
| chr3:149169038 | C | CGTGTGTG others(5): Show |
6 | a0001c0002t0013g0009 a0001c0003t0015g0120 a0001c0005t0015g0041 others(3): Show |
9 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2887+1064_2887+107 others(16): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149169038 | ||||||
| chr3:149169038 | C | T | 1 | a0001c0002t0008g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2887+1055C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169038 | |||||||
| chr3:149169140 | AT | A | 16 | a0001c0002t0012g0129 a0001c0002t0013g0009 a0001c0002t0035g0065 others(13): Show |
20 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2887+1163delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149169140 | ||||||
| chr3:149169224 | G | C | 6 | a0001c0002t0006g0148 a0001c0002t0006g0149 a0001c0002t0006g0150 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2887+1241G>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169224 | |||||||
| chr3:149169385 | T | C | 43 | a0001c0001t0003g0036 a0001c0001t0003g0066 a0001c0001t0003g0075 others(40): Show |
56 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2887+1402T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169385 | |||||||
| chr3:149169443 | A | T | 16 | a0001c0002t0012g0129 a0001c0002t0013g0009 a0001c0002t0035g0065 others(13): Show |
20 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2887+1460A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169443 | |||||||
| chr3:149169702 | A | T | 7 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(4): Show |
7 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2887+1719A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169702 | |||||||
| chr3:149169937 | T | C | 4 | a0001c0003t0001g0038 a0001c0003t0001g0245 a0001c0003t0001g0247 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2887+1954T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169937 | |||||||
| chr3:149169965 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2887+1982G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169965 | |||||||
| chr3:149169979 | G | A | 1 | a0001c0002t0006g0148 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2887+1996G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149169979 | |||||||
| chr3:149170028 | C | A | 20 | a0001c0001t0001g0110 a0001c0001t0008g0084 a0001c0001t0041g0111 others(17): Show |
20 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2887+2045C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170028 | |||||||
| chr3:149170034 | T | G | 3 | a0001c0003t0015g0120 a0001c0005t0015g0041 a0001c0005t0036g0292 |
4 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2887+2051T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170034 | |||||||
| chr3:149170217 | T | G | 13 | a0001c0002t0012g0129 a0001c0002t0013g0009 a0001c0002t0035g0065 others(10): Show |
16 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2888-1878T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170217 | |||||||
| chr3:149170355 | G | A | 1 | a0001c0005t0031g0286 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2888-1740G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170355 | |||||||
| chr3:149170435 | C | T | 1 | a0001c0004t0025g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2888-1660C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170435 | |||||||
| chr3:149170521 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2888-1574T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170521 | |||||||
| chr3:149170801 | C | T | 3 | a0001c0003t0015g0120 a0001c0005t0015g0041 a0001c0005t0036g0292 |
4 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2888-1294C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170801 | |||||||
| chr3:149170802 | G | A | 4 | a0001c0002t0013g0009 a0001c0002t0035g0065 a0001c0005t0040g0287 others(1): Show |
6 | HG02622.hp2 HG03195.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2888-1293G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170802 | |||||||
| chr3:149170832 | A | T | 1 | a0001c0003t0001g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2888-1263A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170832 | |||||||
| chr3:149170873 | G | A | 54 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(51): Show |
67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.2888-1222G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149170873 | |||||||
| chr3:149171008 | G | A | 1 | a0001c0005t0023g0074 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2888-1087G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171008 | |||||||
| chr3:149171017 | C | T | 4 | a0001c0002t0030g0145 a0001c0005t0023g0074 a0001c0005t0026g0071 others(1): Show |
4 | HG01346.hp2 HG01358.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2888-1078C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171017 | |||||||
| chr3:149171018 | G | A | 1 | a0005c0010t0002g0013 | 3 | NA18962.hp2 NA19063.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2888-1077G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171018 | |||||||
| chr3:149171054 | C | T | 2 | a0001c0001t0003g0036 a0001c0002t0003g0165 |
3 | NA18970.hp1 NA19064.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2888-1041C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171054 | |||||||
| chr3:149171104 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2888-991C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171104 | |||||||
| chr3:149171149 | G | A | 54 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(51): Show |
67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.2888-946G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171149 | |||||||
| chr3:149171194 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2888-901C>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171194 | |||||||
| chr3:149171233 | G | A | 1 | a0001c0002t0002g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2888-862G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171233 | |||||||
| chr3:149171264 | G | A | 3 | a0001c0003t0015g0120 a0001c0005t0015g0041 a0001c0005t0036g0292 |
4 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2888-831G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171264 | |||||||
| chr3:149171276 | C | CA | 50 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(47): Show |
63 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2888-807dupA | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149171276 | ||||||
| chr3:149171287 | A | T | 5 | a0001c0002t0030g0145 a0001c0005t0023g0074 a0001c0005t0026g0071 others(2): Show |
5 | HG01346.hp2 HG01358.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.2888-808A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171287 | |||||||
| chr3:149171398 | C | T | 2 | a0001c0005t0019g0134 a0001c0005t0019g0135 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2888-697C>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171398 | |||||||
| chr3:149171426 | T | TCAAA | 124 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(121): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2888-666_2888-665i others(6): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149171426 | ||||||
| chr3:149171440 | T | G | 54 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0209 others(51): Show |
67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.2888-655T>G | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171440 | |||||||
| chr3:149171448 | G | A | 1 | a0001c0003t0001g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2888-647G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171448 | |||||||
| chr3:149171660 | T | C | 1 | a0001c0002t0003g0161 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2888-435T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171660 | |||||||
| chr3:149171698 | C | CT | 16 | a0001c0001t0001g0110 a0001c0001t0001g0184 a0001c0001t0011g0215 others(13): Show |
17 | HG00735.hp2 HG01169.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2888-378dupT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149171698 | ||||||
| chr3:149171698 | C | CTT | 10 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(7): Show |
12 | HG02109.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2888-379_2888-378d others(4): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149171698 | ||||||
| chr3:149171698 | C | CTTT | 9 | a0001c0002t0010g0048 a0001c0002t0012g0129 a0001c0005t0010g0288 others(6): Show |
10 | HG00738.hp2 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.2888-380_2888-378d others(5): Show |
HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149171698 | ||||||
| chr3:149171698 | CT | C | 62 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0002g0035 others(59): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2888-378delT | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 149171698 | ||||||
| chr3:149171717 | T | C | 1 | a0001c0006t0001g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2888-378T>C | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171717 | |||||||
| chr3:149171812 | C | A | 1 | a0001c0004t0002g0088 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2888-283C>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171812 | |||||||
| chr3:149171817 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2888-278G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171817 | |||||||
| chr3:149171854 | G | A | 11 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(8): Show |
13 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2888-241G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171854 | |||||||
| chr3:149171862 | G | A | 1 | a0001c0015t0001g0213 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2888-233G>A | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149171862 | |||||||
| chr3:149172040 | A | T | 7 | a0001c0002t0010g0043 a0001c0002t0010g0044 a0001c0002t0010g0045 others(4): Show |
7 | HG00738.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2888-55A>T | HPS3 | ENSG00000163755.9 | transcript | ENST00000296051.7 | protein_coding | 16/16 | chr3 | 149172040 |