| geneid | 55023 |
|---|---|
| ensemblid | ENSG00000146247.15 |
| hgncid | 15673 |
| symbol | PHIP |
| name | pleckstrin homology domain interacting protein |
| refseq_nuc | NM_017934.7 |
| refseq_prot | NP_060404.4 |
| ensembl_nuc | ENST00000275034.5 |
| ensembl_prot | ENSP00000275034.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 78934419 |
| end | 79078254 |
| strand | - |
| ver | v1.2 |
| region | chr6:78934419-79078254 |
| region5000 | chr6:78929419-79083254 |
| regionname0 | PHIP_chr6_78934419_79078254 |
| regionname5000 | PHIP_chr6_78929419_79083254 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1821 | 178 | 72 | 24 | 62 | 2 | 17 | 52 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002 | 0/0 | 1821 | 85 | 14 | 16 | 39 | 6 | 10 | 32 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003 | 0/0 | 1821 | 33 | 2 | 5 | 19 | 4 | 3 | 13 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0004 | 1/0 | 1821 | 18 | 5 | 9 | 0 | 0 | 3 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0005 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0006 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0007 | 0/0 | 1821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0008 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 5466 | 123 | 30 | 21 | 52 | 2 | 17 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0002 | 0/0 | 5466 | 79 | 14 | 11 | 38 | 6 | 10 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0003 | 0/0 | 5466 | 33 | 2 | 5 | 19 | 4 | 3 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0004 | 1/0 | 5466 | 18 | 5 | 9 | 0 | 0 | 3 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0005 | 0/0 | 5466 | 17 | 16 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0006 | 0/0 | 5466 | 17 | 9 | 1 | 7 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0007 | 0/0 | 5466 | 7 | 7 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0008 | 0/0 | 5466 | 4 | 4 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0009 | 0/0 | 5466 | 4 | 0 | 4 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0010 | 0/0 | 5466 | 3 | 2 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0011 | 0/0 | 5466 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0012 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0013 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0014 | 0/0 | 5466 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0015 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0016 | 0/0 | 5466 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0017 | 0/0 | 5466 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0018 | 0/0 | 5466 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0019 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0020 | 0/0 | 5466 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| c0021 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 6462 | 61 | 5 | 12 | 32 | 1 | 10 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0002 | 0/0 | 6459 | 34 | 8 | 4 | 18 | 3 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0003 | 0/0 | 6463 | 30 | 8 | 5 | 12 | 1 | 4 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0004 | 0/0 | 6459 | 23 | 1 | 5 | 11 | 2 | 4 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0005 | 0/0 | 6463 | 22 | 2 | 3 | 13 | 0 | 4 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0006 | 0/0 | 6461 | 12 | 0 | 9 | 0 | 0 | 3 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0007 | 0/0 | 6462 | 11 | 5 | 3 | 0 | 3 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0008 | 0/0 | 6464 | 9 | 4 | 0 | 4 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0009 | 0/0 | 6460 | 7 | 2 | 0 | 3 | 1 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0010 | 0/0 | 6460 | 7 | 0 | 0 | 6 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0011 | 0/0 | 6463 | 6 | 6 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0012 | 0/0 | 6463 | 6 | 6 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0013 | 0/0 | 6461 | 5 | 5 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0014 | 0/0 | 6465 | 4 | 1 | 1 | 0 | 0 | 2 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0015 | 0/0 | 6464 | 4 | 1 | 1 | 0 | 0 | 2 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0016 | 0/0 | 6472 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0017 | 0/0 | 6464 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0018 | 0/0 | 6464 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0019 | 0/0 | 6463 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0020 | 0/0 | 6462 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0021 | 0/0 | 6463 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0022 | 0/0 | 6459 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0023 | 0/0 | 6465 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0024 | 0/0 | 6466 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0025 | 0/0 | 6463 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0026 | 0/0 | 6463 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0027 | 0/0 | 6465 | 2 | 0 | 1 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0028 | 0/0 | 6463 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0029 | 0/0 | 6463 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0030 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0031 | 0/0 | 6458 | 2 | 0 | 1 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0032 | 0/0 | 6464 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0033 | 0/0 | 6464 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0034 | 0/0 | 6463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0035 | 0/0 | 6463 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0036 | 0/0 | 6463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0037 | 0/0 | 6462 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0038 | 0/0 | 6463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0039 | 0/0 | 6462 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0040 | 0/0 | 6462 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0041 | 0/0 | 6462 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0042 | 0/0 | 6462 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0043 | 0/0 | 6458 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0044 | 0/0 | 6461 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0045 | 0/0 | 6462 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0046 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0047 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0048 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0049 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0050 | 0/0 | 6463 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0051 | 0/0 | 6464 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0052 | 0/0 | 6461 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0053 | 0/0 | 6463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0054 | 0/0 | 6463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0055 | 0/0 | 6463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0056 | 0/0 | 6465 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0057 | 0/0 | 6462 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0058 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0059 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0060 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0061 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0062 | 0/0 | 6461 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0063 | 0/0 | 6461 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0064 | 1/0 | 6461 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0065 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0066 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0067 | 0/0 | 6458 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0068 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| t0069 | 0/0 | 6448 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5466 | 123 | 30 | 21 | 52 | 2 | 17 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005 | 0/0 | 5466 | 17 | 16 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0006 | 0/0 | 5466 | 17 | 9 | 1 | 7 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0007 | 0/0 | 5466 | 7 | 7 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0008 | 0/0 | 5466 | 4 | 4 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0010 | 0/0 | 5466 | 3 | 2 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0011 | 0/0 | 5466 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0012 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0013 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0015 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0021 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002 | 0/0 | 5466 | 79 | 14 | 11 | 38 | 6 | 10 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0009 | 0/0 | 5466 | 4 | 0 | 4 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0014 | 0/0 | 5466 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0020 | 0/0 | 5466 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003 | 0/0 | 5466 | 33 | 2 | 5 | 19 | 4 | 3 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0004c0004 | 1/0 | 5466 | 18 | 5 | 9 | 0 | 0 | 3 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0005c0016 | 0/0 | 5466 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0006c0017 | 0/0 | 5466 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0007c0018 | 0/0 | 5466 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0008c0019 | 0/0 | 5466 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 11927 | 59 | 5 | 12 | 31 | 1 | 9 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0005 | 0/0 | 11928 | 22 | 2 | 3 | 13 | 0 | 4 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0011 | 0/0 | 11928 | 6 | 6 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0014 | 0/0 | 11930 | 4 | 1 | 1 | 0 | 0 | 2 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0015 | 0/0 | 11929 | 4 | 1 | 1 | 0 | 0 | 2 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0017 | 0/0 | 11929 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0018 | 0/0 | 11929 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0021 | 0/0 | 11928 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0025 | 0/0 | 11928 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0026 | 0/0 | 11928 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0032 | 0/0 | 11929 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0033 | 0/0 | 11929 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0034 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0035 | 0/0 | 11928 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0037 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0039 | 0/0 | 11927 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0040 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0041 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0042 | 0/0 | 11927 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0043 | 0/0 | 11923 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0044 | 0/0 | 11926 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0050 | 0/0 | 11928 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0059 | 0/0 | 11924 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0067 | 0/0 | 11923 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0001t0069 | 0/0 | 11913 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0003 | 0/0 | 11928 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0019 | 0/0 | 11928 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0023 | 0/0 | 11930 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0027 | 0/0 | 11930 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0030 | 0/0 | 11924 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0038 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0045 | 0/0 | 11927 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0046 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0049 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0054 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0005t0055 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0006t0002 | 0/0 | 11924 | 11 | 6 | 1 | 4 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0006t0008 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0006t0009 | 0/0 | 11925 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0006t0020 | 0/0 | 11927 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0007t0012 | 0/0 | 11928 | 6 | 6 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0007t0047 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0008t0003 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0008t0007 | 0/0 | 11927 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0010t0029 | 0/0 | 11928 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0010t0057 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0011t0016 | 0/0 | 11937 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0012t0024 | 0/0 | 11931 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0013t0007 | 0/0 | 11927 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0015t0024 | 0/0 | 11931 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0001c0021t0036 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0003 | 0/0 | 11928 | 25 | 4 | 4 | 12 | 1 | 4 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0004 | 0/0 | 11924 | 18 | 1 | 1 | 10 | 2 | 4 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0007 | 0/0 | 11927 | 7 | 1 | 3 | 0 | 3 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0008 | 0/0 | 11929 | 8 | 3 | 0 | 4 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0010 | 0/0 | 11925 | 7 | 0 | 0 | 6 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0022 | 0/0 | 11924 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0027 | 0/0 | 11930 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0028 | 0/0 | 11928 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0048 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0051 | 0/0 | 11929 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0053 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0056 | 0/0 | 11930 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0058 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0062 | 0/0 | 11926 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0063 | 0/0 | 11926 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0066 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0002t0068 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0009t0004 | 0/0 | 11924 | 4 | 0 | 4 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0014t0003 | 0/0 | 11928 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0002c0020t0022 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003t0002 | 0/0 | 11924 | 23 | 2 | 3 | 14 | 3 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003t0009 | 0/0 | 11925 | 5 | 0 | 0 | 3 | 1 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003t0031 | 0/0 | 11923 | 2 | 0 | 1 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003t0052 | 0/0 | 11926 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003t0060 | 0/0 | 11924 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0003c0003t0061 | 0/0 | 11924 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0004c0004t0006 | 0/0 | 11926 | 12 | 0 | 9 | 0 | 0 | 3 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0004c0004t0013 | 0/0 | 11926 | 4 | 4 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0004c0004t0064 | 1/0 | 11926 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0004c0004t0065 | 0/0 | 11925 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0005c0016t0001 | 0/0 | 11927 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0006c0017t0004 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0007c0018t0001 | 0/0 | 11927 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| a0008c0019t0013 | 0/0 | 11926 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | copy fasta | chr6 | 78929419 | 79083254 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0014g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0014g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0015g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0015g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0017g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0018g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0021g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0021g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0025g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0026g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0026g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0032g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0033g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0034g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0035g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0037g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0039g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0040g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0041g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0042g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0043g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0044g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0050g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0059g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0067g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0001t0069g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0019g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0019g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0023g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0027g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0030g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0030g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0038g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0045g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0046g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0049g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0054g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0005t0055g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0020g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0006t0020g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0007t0047g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0008t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0008t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0008t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0008t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0010t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0010t0029g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0010t0057g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0011t0016g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0011t0016g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0011t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0012t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0013t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0015t0024g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0001c0021t0036g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0007g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0007g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0022g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0022g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0027g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0028g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0028g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0048g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0051g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0053g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0056g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0058g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0062g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0063g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0066g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0002t0068g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0009t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0009t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0009t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0014t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0002c0020t0022g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0009g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0009g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0009g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0031g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0031g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0052g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0060g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0003c0003t0061g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0064g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0004c0004t0065g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0005c0016t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0006c0017t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0007c0018t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| a0008c0019t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0007 | g0004 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0286 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00140 | hp2 | a0002 | c0002 | t0007 | g0004 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00280 | hp1 | a0002 | c0002 | t0007 | g0003 | EUR | FIN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00280 | hp2 | a0001 | c0001 | t0033 | g0021 | EUR | FIN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00438 | hp2 | a0003 | c0003 | t0052 | g0298 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00558 | hp1 | a0002 | c0002 | t0010 | g0224 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00558 | hp2 | a0005 | c0016 | t0001 | g0126 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00621 | hp1 | a0002 | c0002 | t0004 | g0198 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00639 | hp1 | a0001 | c0001 | t0015 | g0159 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00639 | hp2 | a0001 | c0001 | t0037 | g0055 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00642 | hp1 | a0001 | c0001 | t0040 | g0079 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00642 | hp2 | a0002 | c0014 | t0003 | g0210 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00673 | hp2 | a0002 | c0002 | t0008 | g0240 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00733 | hp1 | a0002 | c0002 | t0004 | g0216 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00735 | hp1 | a0003 | c0003 | t0002 | g0279 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00735 | hp2 | a0004 | c0004 | t0006 | g0008 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00738 | hp1 | a0002 | c0009 | t0004 | g0259 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01069 | hp1 | a0002 | c0002 | t0007 | g0039 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01070 | hp1 | a0003 | c0003 | t0031 | g0273 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01071 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0059 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01106 | hp1 | a0002 | c0009 | t0004 | g0214 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01106 | hp2 | a0004 | c0004 | t0006 | g0008 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0193 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01109 | hp2 | a0001 | c0005 | t0027 | g0033 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01175 | hp1 | a0001 | c0001 | t0014 | g0160 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0288 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01255 | hp2 | a0004 | c0004 | t0006 | g0185 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01257 | hp2 | a0002 | c0009 | t0004 | g0009 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01258 | hp1 | a0001 | c0001 | t0044 | g0056 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01258 | hp2 | a0002 | c0009 | t0004 | g0009 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01261 | hp1 | a0002 | c0002 | t0007 | g0040 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01261 | hp2 | a0003 | c0003 | t0060 | g0280 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01346 | hp2 | a0003 | c0003 | t0002 | g0274 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01358 | hp1 | a0001 | c0010 | t0057 | g0163 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01358 | hp2 | a0004 | c0004 | t0006 | g0187 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01496 | hp1 | a0001 | c0001 | t0041 | g0135 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01496 | hp2 | a0004 | c0004 | t0006 | g0180 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0015 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01516 | hp2 | a0002 | c0002 | t0004 | g0232 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01517 | hp1 | a0002 | c0002 | t0004 | g0215 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01517 | hp2 | a0003 | c0003 | t0002 | g0015 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01884 | hp1 | a0004 | c0004 | t0013 | g0165 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01884 | hp2 | a0001 | c0005 | t0030 | g0048 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0031 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01891 | hp2 | a0001 | c0006 | t0009 | g0266 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01934 | hp1 | a0004 | c0004 | t0006 | g0007 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01952 | hp2 | a0004 | c0004 | t0006 | g0007 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01975 | hp1 | a0004 | c0004 | t0006 | g0181 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0249 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01978 | hp2 | a0004 | c0004 | t0006 | g0189 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01981 | hp2 | a0002 | c0002 | t0028 | g0261 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02004 | hp1 | a0002 | c0002 | t0028 | g0260 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02027 | hp1 | a0001 | c0001 | t0035 | g0067 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0287 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0152 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0246 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0281 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02080 | hp2 | a0002 | c0002 | t0010 | g0206 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0162 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02145 | hp2 | a0001 | c0001 | t0034 | g0132 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02148 | hp1 | a0002 | c0002 | t0051 | g0248 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02155 | hp2 | a0003 | c0003 | t0002 | g0292 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02165 | hp1 | a0001 | c0001 | t0032 | g0090 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0290 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02257 | hp1 | a0004 | c0004 | t0013 | g0166 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02258 | hp1 | a0001 | c0006 | t0002 | g0014 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0255 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02280 | hp1 | a0001 | c0005 | t0003 | g0001 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02280 | hp2 | a0001 | c0008 | t0007 | g0168 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0041 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02523 | hp1 | a0003 | c0003 | t0002 | g0296 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02523 | hp2 | a0002 | c0002 | t0004 | g0221 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02572 | hp1 | a0001 | c0006 | t0008 | g0037 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02572 | hp2 | a0002 | c0002 | t0048 | g0020 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0205 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02622 | hp1 | a0001 | c0008 | t0007 | g0167 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02622 | hp2 | a0001 | c0007 | t0012 | g0177 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0294 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02683 | hp2 | a0002 | c0002 | t0010 | g0222 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0211 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02717 | hp1 | a0002 | c0002 | t0008 | g0192 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02723 | hp1 | a0001 | c0005 | t0054 | g0038 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02723 | hp2 | a0001 | c0006 | t0002 | g0265 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0245 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02809 | hp1 | a0001 | c0007 | t0047 | g0178 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0151 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02818 | hp1 | a0001 | c0005 | t0038 | g0047 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02818 | hp2 | a0002 | c0002 | t0063 | g0179 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02886 | hp1 | a0001 | c0006 | t0009 | g0297 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02886 | hp2 | a0001 | c0005 | t0045 | g0046 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02895 | hp1 | a0004 | c0004 | t0065 | g0183 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02895 | hp2 | a0001 | c0006 | t0002 | g0267 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0256 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02896 | hp2 | a0001 | c0007 | t0012 | g0175 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02897 | hp1 | a0004 | c0004 | t0013 | g0182 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02897 | hp2 | a0001 | c0007 | t0012 | g0174 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02922 | hp1 | a0001 | c0007 | t0012 | g0172 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0028 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02965 | hp1 | a0001 | c0005 | t0003 | g0001 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02965 | hp2 | a0001 | c0010 | t0029 | g0054 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02970 | hp1 | a0002 | c0002 | t0008 | g0197 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02970 | hp2 | a0001 | c0001 | t0018 | g0258 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02976 | hp1 | a0001 | c0005 | t0023 | g0049 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0149 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03017 | hp1 | a0004 | c0004 | t0006 | g0186 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03041 | hp1 | a0001 | c0005 | t0019 | g0012 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03041 | hp2 | a0001 | c0013 | t0007 | g0169 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0026 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03098 | hp2 | a0002 | c0002 | t0003 | g0042 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03130 | hp1 | a0001 | c0005 | t0019 | g0012 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03139 | hp2 | a0002 | c0002 | t0053 | g0194 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03195 | hp1 | a0002 | c0002 | t0058 | g0043 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03195 | hp2 | a0001 | c0006 | t0002 | g0269 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03209 | hp1 | a0001 | c0006 | t0002 | g0270 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03209 | hp2 | a0001 | c0015 | t0024 | g0035 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03225 | hp1 | a0001 | c0005 | t0055 | g0045 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03225 | hp2 | a0002 | c0002 | t0056 | g0196 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0233 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0254 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0257 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03492 | hp1 | a0001 | c0001 | t0015 | g0156 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03516 | hp1 | a0001 | c0005 | t0046 | g0263 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03540 | hp1 | a0001 | c0007 | t0012 | g0176 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03540 | hp2 | a0003 | c0003 | t0002 | g0295 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03579 | hp1 | a0001 | c0010 | t0029 | g0053 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03579 | hp2 | a0001 | c0001 | t0026 | g0154 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03654 | hp1 | a0004 | c0004 | t0006 | g0191 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03654 | hp2 | a0001 | c0001 | t0014 | g0161 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03669 | hp1 | a0002 | c0002 | t0008 | g0209 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0095 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03831 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0091 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03834 | hp1 | a0004 | c0004 | t0006 | g0188 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0065 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03942 | hp2 | a0001 | c0001 | t0015 | g0155 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04115 | hp2 | a0001 | c0001 | t0014 | g0158 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0244 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0052 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0010 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04199 | hp2 | a0003 | c0003 | t0009 | g0272 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04204 | hp2 | a0002 | c0002 | t0004 | g0207 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04228 | hp1 | a0007 | c0018 | t0001 | g0085 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG04228 | hp2 | a0003 | c0003 | t0061 | g0283 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0153 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18522 | hp2 | a0001 | c0005 | t0023 | g0051 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18612 | hp2 | a0002 | c0002 | t0004 | g0229 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18747 | hp2 | a0002 | c0002 | t0004 | g0213 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18906 | hp1 | a0001 | c0001 | t0021 | g0030 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18906 | hp2 | a0001 | c0005 | t0030 | g0050 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18941 | hp2 | a0002 | c0002 | t0004 | g0227 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18943 | hp1 | a0003 | c0003 | t0002 | g0282 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18944 | hp1 | a0001 | c0006 | t0020 | g0006 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18944 | hp2 | a0001 | c0001 | t0043 | g0104 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18945 | hp1 | a0001 | c0001 | t0042 | g0088 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18950 | hp2 | a0003 | c0003 | t0009 | g0277 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18959 | hp2 | a0002 | c0002 | t0004 | g0236 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18962 | hp1 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18964 | hp2 | a0003 | c0003 | t0002 | g0289 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18965 | hp1 | a0002 | c0002 | t0004 | g0223 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18965 | hp2 | a0001 | c0006 | t0020 | g0148 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0202 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0284 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18978 | hp2 | a0002 | c0002 | t0008 | g0204 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0201 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18982 | hp2 | a0002 | c0002 | t0022 | g0225 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18984 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18984 | hp2 | a0001 | c0001 | t0050 | g0061 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18985 | hp2 | a0002 | c0002 | t0010 | g0234 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0278 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18988 | hp1 | a0002 | c0002 | t0022 | g0235 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18989 | hp1 | a0002 | c0002 | t0010 | g0228 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18989 | hp2 | a0003 | c0003 | t0031 | g0293 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18991 | hp2 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18995 | hp1 | a0001 | c0001 | t0067 | g0063 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18995 | hp2 | a0006 | c0017 | t0004 | g0226 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18998 | hp1 | a0001 | c0006 | t0020 | g0006 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18999 | hp2 | a0002 | c0002 | t0008 | g0247 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19000 | hp1 | a0002 | c0002 | t0008 | g0200 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19002 | hp1 | a0003 | c0003 | t0009 | g0016 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19002 | hp2 | a0002 | c0002 | t0010 | g0218 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19003 | hp1 | a0001 | c0011 | t0016 | g0017 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19007 | hp1 | a0002 | c0002 | t0010 | g0212 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0237 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19011 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19012 | hp1 | a0002 | c0002 | t0003 | g0252 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19012 | hp2 | a0001 | c0001 | t0069 | g0117 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19030 | hp1 | a0001 | c0008 | t0003 | g0170 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19030 | hp2 | a0001 | c0005 | t0049 | g0036 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19043 | hp1 | a0001 | c0005 | t0019 | g0264 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19043 | hp2 | a0001 | c0005 | t0003 | g0001 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19056 | hp2 | a0002 | c0002 | t0068 | g0220 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19057 | hp1 | a0001 | c0006 | t0002 | g0268 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19058 | hp1 | a0002 | c0002 | t0066 | g0230 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19060 | hp1 | a0003 | c0003 | t0002 | g0285 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19064 | hp2 | a0002 | c0002 | t0027 | g0239 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19065 | hp1 | a0001 | c0001 | t0039 | g0083 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19065 | hp2 | a0001 | c0011 | t0016 | g0018 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19068 | hp1 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19070 | hp1 | a0001 | c0006 | t0002 | g0275 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19079 | hp1 | a0002 | c0002 | t0004 | g0219 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19081 | hp1 | a0002 | c0020 | t0022 | g0253 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19081 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0238 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19085 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19089 | hp2 | a0002 | c0002 | t0062 | g0199 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19090 | hp1 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19091 | hp1 | a0002 | c0002 | t0004 | g0231 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19091 | hp2 | a0001 | c0011 | t0016 | g0019 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19240 | hp1 | a0001 | c0006 | t0002 | g0014 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA19240 | hp2 | a0001 | c0008 | t0007 | g0171 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA20129 | hp1 | a0001 | c0001 | t0025 | g0024 | AFR | ASW | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA20129 | hp2 | a0001 | c0001 | t0021 | g0027 | AFR | ASW | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA20752 | hp1 | a0003 | c0003 | t0009 | g0276 | EUR | TSI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0251 | EUR | TSI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01123 | hp1 | a0001 | c0006 | t0002 | g0271 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0250 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02109 | hp1 | a0001 | c0001 | t0025 | g0025 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02109 | hp2 | a0002 | c0002 | t0007 | g0044 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02486 | hp1 | a0003 | c0003 | t0002 | g0291 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0195 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02559 | hp1 | a0001 | c0001 | t0059 | g0118 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG02559 | hp2 | a0001 | c0007 | t0012 | g0173 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0157 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG03471 | hp2 | a0001 | c0012 | t0024 | g0034 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG06807 | hp1 | a0004 | c0004 | t0013 | g0184 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| HG06807 | hp2 | a0002 | c0002 | t0004 | g0217 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18955 | hp1 | a0003 | c0003 | t0009 | g0016 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA20300 | hp1 | a0001 | c0021 | t0036 | g0070 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| NA21309 | hp2 | a0008 | c0019 | t0013 | g0190 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0128 | REF | REF | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| homoSapiens_grch38 | hp1 | a0004 | c0004 | t0064 | g0164 | REF | REF | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:78946145
|
C | T | 1 | a0006 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.4486G>A | p.Gly1496Ser | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 38/40 | 4672/11926 | 4486/5466 | 1496/1821 | chr6 | 78946145 | ||
| chr6:78963145
|
C | T | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.3487G>A | p.Glu1163Lys | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/40 | 3673/11926 | 3487/5466 | 1163/1821 | chr6 | 78963145 | ||
| chr6:78965984
|
A | G | 2 | a0002a0006 | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
missense_variant | MODERATE | c.3278T>C | p.Leu1093Pro | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 28/40 | 3464/11926 | 3278/5466 | 1093/1821 | chr6 | 78965984 | ||
| chr6:78983034
|
G | A | 1 | a0003 | 33 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(30): Show |
missense_variant | MODERATE | c.2621C>T | p.Thr874Ile | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/40 | 2807/11926 | 2621/5466 | 874/1821 | chr6 | 78983034 | ||
| chr6:78997475
|
G | A | 1 | a0007 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2140C>T | p.Arg714Trp | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/40 | 2326/11926 | 2140/5466 | 714/1821 | chr6 | 78997475 | ||
| chr6:78998283
|
A | C | 6 | a0001a0002a0003others(3): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
missense_variant | MODERATE | c.1988T>G | p.Val663Gly | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/40 | 2174/11926 | 1988/5466 | 663/1821 | chr6 | 78998283 | ||
| chr6:79015709
|
T | C | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1310A>G | p.Asn437Ser | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 14/40 | 1496/11926 | 1310/5466 | 437/1821 | chr6 | 79015709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:78946760
|
T | G | 1 | a0001c0011 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
synonymous_variant | LOW | c.4321A>C | p.Arg1441Arg | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4507/11926 | 4321/5466 | 1441/1821 | chr6 | 78946760 | ||
| chr6:78946800
|
A | G | 1 | a0001c0013 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.4281T>C | p.Ser1427Ser | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4467/11926 | 4281/5466 | 1427/1821 | chr6 | 78946800 | ||
| chr6:78946845
|
A | T | 7 | a0001c0008a0001c0013a0002c0002others(4): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
synonymous_variant | LOW | c.4236T>A | p.Ala1412Ala | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4422/11926 | 4236/5466 | 1412/1821 | chr6 | 78946845 | ||
| chr6:78946853
|
G | A | 9 | a0001c0007a0001c0008a0001c0010others(6): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
synonymous_variant | LOW | c.4228C>T | p.Leu1410Leu | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4414/11926 | 4228/5466 | 1410/1821 | chr6 | 78946853 | ||
| chr6:78947674
|
G | A | 4 | a0001c0001a0001c0021a0005c0016others(1): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
synonymous_variant | LOW | c.4155C>T | p.Val1385Val | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/40 | 4341/11926 | 4155/5466 | 1385/1821 | chr6 | 78947674 | ||
| chr6:78969860
|
A | G | 8 | a0001c0001a0001c0005a0001c0011others(5): Show | 148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
synonymous_variant | LOW | c.3180T>C | p.Asp1060Asp | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/40 | 3366/11926 | 3180/5466 | 1060/1821 | chr6 | 78969860 | ||
| chr6:78978649
|
T | C | 1 | a0002c0009 | 4 | HG00738.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.2832A>G | p.Thr944Thr | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/40 | 3018/11926 | 2832/5466 | 944/1821 | chr6 | 78978649 | ||
| chr6:78990931
|
C | T | 2 | a0001c0012a0001c0015 | 2 | HG03209.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2256G>A | p.Arg752Arg | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/40 | 2442/11926 | 2256/5466 | 752/1821 | chr6 | 78990931 | ||
| chr6:78997467
|
C | A | 1 | a0001c0011 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
synonymous_variant | LOW | c.2148G>T | p.Leu716Leu | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/40 | 2334/11926 | 2148/5466 | 716/1821 | chr6 | 78997467 | ||
| chr6:79017564
|
C | T | 1 | a0001c0007 | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.1014G>A | p.Thr338Thr | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 11/40 | 1200/11926 | 1014/5466 | 338/1821 | chr6 | 79017564 | ||
| chr6:79019114
|
T | C | 1 | a0002c0020 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.969A>G | p.Gln323Gln | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/40 | 1155/11926 | 969/5466 | 323/1821 | chr6 | 79019114 | ||
| chr6:79026042
|
T | C | 1 | a0001c0021 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.723A>G | p.Ala241Ala | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 8/40 | 909/11926 | 723/5466 | 241/1821 | chr6 | 79026042 | ||
| chr6:79026162
|
A | G | 1 | a0002c0014 | 1 | HG00642.hp2 | splice_region_variant&synonymous_variant | LOW | c.603T>C | p.Gly201Gly | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 8/40 | 789/11926 | 603/5466 | 201/1821 | chr6 | 79026162 | ||
| chr6:79042879
|
A | G | 2 | a0001c0008a0001c0013 | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.564T>C | p.Cys188Cys | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/40 | 750/11926 | 564/5466 | 188/1821 | chr6 | 79042879 | ||
| chr6:79042993
|
C | G | 1 | a0001c0012 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.450G>C | p.Leu150Leu | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/40 | 636/11926 | 450/5466 | 150/1821 | chr6 | 79042993 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:78934770
|
C | G | 1 | a0001c0001t0059 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5923G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5923 | chr6 | 78934770 | |||||
| chr6:78935410
|
ATT | A | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5281_*5282delAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5281 | chr6 | 78935410 | |||||
| chr6:78935440
|
C | CCCTTT | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5252_*5253insAAAG others(1): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5252 | chr6 | 78935440 | |||||
| chr6:78935449
|
CTTT | C | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5241_*5243delAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5241 | chr6 | 78935449 | |||||
| chr6:78935505
|
G | A | 1 | a0001c0001t0035 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5188C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5188 | chr6 | 78935505 | |||||
| chr6:78936028
|
G | A | 1 | a0001c0001t0026 | 2 | HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4665C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4665 | chr6 | 78936028 | |||||
| chr6:78936060
|
C | T | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4633G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4633 | chr6 | 78936060 | |||||
| chr6:78936203
|
A | C | 2 | a0001c0001t0037a0001c0001t0044 | 2 | HG00639.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4490T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4490 | chr6 | 78936203 | |||||
| chr6:78936330
|
A | G | 2 | a0002c0002t0022a0002c0020t0022 | 3 | NA18982.hp2 NA18988.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4363T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4363 | chr6 | 78936330 | |||||
| chr6:78936406
|
A | C | 3 | a0001c0001t0059a0001c0005t0023a0001c0005t0030 | 5 | HG01884.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4287T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4287 | chr6 | 78936406 | |||||
| chr6:78936437
|
T | C | 1 | a0002c0002t0028 | 2 | HG01981.hp2 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4256A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4256 | chr6 | 78936437 | |||||
| chr6:78936723
|
T | C | 1 | a0001c0005t0049 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3970A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3970 | chr6 | 78936723 | |||||
| chr6:78936816
|
A | G | 1 | a0001c0001t0034 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3877T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3877 | chr6 | 78936816 | |||||
| chr6:78936846
|
G | T | 1 | a0001c0001t0033 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3847C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3847 | chr6 | 78936846 | |||||
| chr6:78936858
|
A | G | 30 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(27): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3835T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3835 | chr6 | 78936858 | |||||
| chr6:78937114
|
C | T | 1 | a0001c0021t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3579G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3579 | chr6 | 78937114 | |||||
| chr6:78937256
|
T | C | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3437A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3437 | chr6 | 78937256 | |||||
| chr6:78937530
|
A | G | 1 | a0001c0021t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3163T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3163 | chr6 | 78937530 | |||||
| chr6:78937646
|
G | A | 3 | a0001c0001t0014a0001c0001t0015a0001c0001t0033 | 9 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3047C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3047 | chr6 | 78937646 | |||||
| chr6:78937678
|
G | A | 1 | a0001c0010t0029 | 2 | HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3015C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3015 | chr6 | 78937678 | |||||
| chr6:78937690
|
GT | G | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0032others(14): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3002delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3002 | chr6 | 78937690 | |||||
| chr6:78937695
|
T | C | 1 | a0004c0004t0006 | 12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2998A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2998 | chr6 | 78937695 | |||||
| chr6:78937727
|
T | C | 2 | a0001c0005t0038a0001c0005t0045 | 2 | HG02818.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2966A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2966 | chr6 | 78937727 | |||||
| chr6:78937732
|
G | C | 1 | a0001c0001t0039 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2961C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2961 | chr6 | 78937732 | |||||
| chr6:78937869
|
G | A | 2 | a0001c0005t0054a0001c0005t0055 | 2 | HG02723.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2824C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2824 | chr6 | 78937869 | |||||
| chr6:78937959
|
G | A | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2734C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2734 | chr6 | 78937959 | |||||
| chr6:78937994
|
A | G | 1 | a0003c0003t0061 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2699T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2699 | chr6 | 78937994 | |||||
| chr6:78938311
|
A | G | 2 | a0001c0001t0017a0001c0001t0025 | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2382T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2382 | chr6 | 78938311 | |||||
| chr6:78938315
|
G | A | 1 | a0001c0005t0055 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2378C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2378 | chr6 | 78938315 | |||||
| chr6:78938333
|
A | G | 1 | a0001c0010t0057 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2360 | chr6 | 78938333 | |||||
| chr6:78938547
|
A | G | 2 | a0001c0007t0012a0001c0007t0047 | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2146T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2146 | chr6 | 78938547 | |||||
| chr6:78938667
|
T | G | 1 | a0002c0002t0053 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2026A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2026 | chr6 | 78938667 | |||||
| chr6:78938953
|
T | G | 1 | a0001c0001t0040 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1740 | chr6 | 78938953 | |||||
| chr6:78938975
|
T | C | 1 | a0002c0002t0051 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1718 | chr6 | 78938975 | |||||
| chr6:78939079
|
A | T | 4 | a0004c0004t0006a0004c0004t0013a0004c0004t0065others(1): Show | 18 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1614T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1614 | chr6 | 78939079 | |||||
| chr6:78939085
|
A | T | 2 | a0002c0002t0048a0002c0002t0053 | 2 | HG02572.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1608T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1608 | chr6 | 78939085 | |||||
| chr6:78939361
|
G | A | 1 | a0001c0006t0020 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1332C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1332 | chr6 | 78939361 | |||||
| chr6:78939524
|
A | T | 1 | a0002c0002t0066 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1169 | chr6 | 78939524 | |||||
| chr6:78939595
|
A | G | 1 | a0003c0003t0060 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1098T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1098 | chr6 | 78939595 | |||||
| chr6:78939894
|
C | A | 1 | a0002c0002t0063 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 799 | chr6 | 78939894 | |||||
| chr6:78939908
|
A | C | 2 | a0001c0007t0012a0001c0007t0047 | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*785T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 785 | chr6 | 78939908 | |||||
| chr6:78939994
|
T | C | 1 | a0001c0001t0041 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*699A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 699 | chr6 | 78939994 | |||||
| chr6:78939996
|
T | C | 1 | a0002c0002t0068 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 697 | chr6 | 78939996 | |||||
| chr6:78940076
|
T | TAA | 76 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(73): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*616_*617insTT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 616 | chr6 | 78940076 | |||||
| chr6:78940120
|
T | C | 1 | a0001c0001t0042 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 573 | chr6 | 78940120 | |||||
| chr6:78940165
|
C | T | 2 | a0001c0005t0019a0001c0005t0046 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 528 | chr6 | 78940165 | |||||
| chr6:78940496
|
TTA | T | 51 | a0001c0001t0050a0001c0001t0067a0001c0005t0003others(48): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*195_*196delTA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 195 | chr6 | 78940496 | |||||
| chr6:78940496
|
TTATA | T | 31 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(28): Show | 133 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*193_*196delTATA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 193 | chr6 | 78940496 | |||||
| chr6:78940543
|
A | AGTTT | 1 | a0001c0001t0021 | 3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*146_*149dupAAAC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 149 | chr6 | 78940543 | |||||
| chr6:78940548
|
G | GT | 8 | a0001c0006t0009a0001c0006t0020a0001c0008t0007others(5): Show | 23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*144dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
G | GTT | 13 | a0001c0005t0003a0001c0005t0019a0001c0005t0054others(10): Show | 48 | HG00438.hp2 HG00642.hp2 HG01074.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*143_*144dupAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
G | GTTT | 10 | a0001c0001t0044a0001c0001t0050a0001c0005t0045others(7): Show | 17 | HG00673.hp2 HG01258.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*142_*144dupAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
G | GTTTT | 15 | a0001c0001t0001a0001c0001t0011a0001c0001t0025others(12): Show | 80 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*141_*144dupAAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
G | GTTTTT | 9 | a0001c0001t0005a0001c0001t0015a0001c0001t0017others(6): Show | 37 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*140_*144dupAAAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
G | GTTTTTT | 3 | a0001c0001t0014a0001c0001t0032a0001c0005t0023 | 7 | HG01175.hp1 HG02145.hp1 HG02165.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*144dupAAAAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
G | T | 1 | a0001c0001t0043 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 145 | chr6 | 78940548 | |||||
| chr6:78940548
|
GT | G | 3 | a0002c0002t0010a0003c0003t0031a0004c0004t0065 | 10 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*144delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | |||||
| chr6:78940548
|
GTT | G | 8 | a0001c0001t0067a0002c0002t0004a0002c0002t0022others(5): Show | 29 | HG00621.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*143_*144delAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 143 | chr6 | 78940548 | |||||
| chr6:78940548
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0069 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135_*144delAAAAAA others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 135 | chr6 | 78940548 | |||||
| chr6:78940551
|
T | G | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 142 | chr6 | 78940551 | |||||
| chr6:78940558
|
T | TTTTGTTT others(6): Show |
1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134_*135insCAAAAC others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 134 | chr6 | 78940558 | |||||
| chr6:79078252
|
A | G | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-184T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/40 | 184 | chr6 | 79078252 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:78941559
|
T | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4829-229A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941559 | ||||||
| chr6:78941599
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-269C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941599 | ||||||
| chr6:78941685
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-355A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941685 | ||||||
| chr6:78941727
|
T | C | 4 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(1): Show | 4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4829-397A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941727 | ||||||
| chr6:78941760
|
G | A | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4829-430C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941760 | ||||||
| chr6:78941955
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4829-625A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941955 | ||||||
| chr6:78942016
|
C | CAGT | 10 | a0004c0004t0006g0007a0004c0004t0006g0008a0004c0004t0006g0180others(7): Show | 12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.4829-689_4829-687d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942016 | ||||||
| chr6:78942202
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4829-872C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942202 | ||||||
| chr6:78942258
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-928C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942258 | ||||||
| chr6:78942311
|
C | T | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.4829-981G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942311 | ||||||
| chr6:78942313
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4829-983A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942313 | ||||||
| chr6:78942616
|
T | C | 10 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(7): Show | 13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.4829-1286A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942616 | ||||||
| chr6:78942665
|
G | C | 1 | a0001c0001t0005g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4829-1335C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942665 | ||||||
| chr6:78942678
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4829-1348A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942678 | ||||||
| chr6:78942751
|
A | C | 1 | a0001c0001t0017g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4829-1421T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942751 | ||||||
| chr6:78942946
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-1616T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942946 | ||||||
| chr6:78943061
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-1731G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943061 | ||||||
| chr6:78943126
|
T | C | 1 | a0004c0004t0013g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4829-1796A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943126 | ||||||
| chr6:78943159
|
G | A | 4 | a0001c0006t0002g0265a0001c0006t0002g0267a0001c0006t0009g0266others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4829-1829C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943159 | ||||||
| chr6:78943171
|
A | C | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4829-1841T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943171 | ||||||
| chr6:78943182
|
C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4829-1852G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943182 | ||||||
| chr6:78943481
|
G | A | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4828+1819C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943481 | ||||||
| chr6:78943490
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4828+1810G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943490 | ||||||
| chr6:78943752
|
C | T | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4828+1548G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943752 | ||||||
| chr6:78943823
|
T | C | 2 | a0004c0004t0006g0187a0004c0004t0006g0188 | 2 | HG01358.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4828+1477A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943823 | ||||||
| chr6:78943889
|
G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4828+1411C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943889 | ||||||
| chr6:78943962
|
G | A | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4828+1338C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943962 | ||||||
| chr6:78943983
|
C | CT | 6 | a0001c0005t0049g0036a0001c0005t0055g0045a0001c0006t0002g0265others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4828+1316dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943983 | ||||||
| chr6:78943988
|
T | TA | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.4828+1311_4828+131 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943988 | ||||||
| chr6:78943988
|
T | TAA | 13 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0092others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.4828+1311_4828+131 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943988 | ||||||
| chr6:78943988
|
T | TAAA | 3 | a0001c0001t0011g0255a0001c0001t0037g0055a0001c0001t0044g0056 | 3 | HG00639.hp2 HG01258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.4828+1311_4828+131 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943988 | ||||||
| chr6:78943989
|
T | A | 127 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.4828+1311A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943989 | ||||||
| chr6:78943989
|
T | TA | 83 | a0001c0001t0001g0089a0001c0007t0012g0173a0001c0007t0012g0174others(80): Show | 87 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.4828+1310_4828+131 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943989 | ||||||
| chr6:78943989
|
T | TAA | 4 | a0001c0010t0057g0163a0002c0002t0003g0262a0002c0002t0008g0246others(1): Show | 4 | HG01358.hp1 HG02055.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828+1310_4828+131 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943989 | ||||||
| chr6:78943990
|
T | A | 222 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(219): Show | 227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.4828+1310A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | ||||||
| chr6:78943990
|
T | TA | 38 | a0001c0006t0002g0013a0001c0006t0002g0268a0001c0006t0002g0269others(35): Show | 44 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.4828+1309dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | ||||||
| chr6:78943990
|
T | TAA | 6 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263others(3): Show | 8 | HG02258.hp1 HG03041.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.4828+1308_4828+130 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | ||||||
| chr6:78943990
|
T | TTA | 2 | a0001c0005t0003g0001a0001c0005t0054g0038 | 4 | HG02280.hp1 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4828+1309_4828+131 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | ||||||
| chr6:78944014
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4828+1286C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944014 | ||||||
| chr6:78944043
|
A | C | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828+1257T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944043 | ||||||
| chr6:78944084
|
G | A | 2 | a0001c0006t0002g0265a0001c0006t0009g0266 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4828+1216C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944084 | ||||||
| chr6:78944437
|
A | T | 96 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.4828+863T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944437 | ||||||
| chr6:78944447
|
G | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828+853C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944447 | ||||||
| chr6:78944852
|
T | G | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4828+448A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944852 | ||||||
| chr6:78944938
|
A | G | 28 | a0001c0001t0011g0029a0001c0001t0011g0150a0001c0001t0011g0151others(25): Show | 28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4828+362T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944938 | ||||||
| chr6:78944939
|
T | C | 1 | a0004c0004t0006g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4828+361A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944939 | ||||||
| chr6:78944968
|
G | GA | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.4828+331dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944968 | ||||||
| chr6:78945082
|
CT | C | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.4828+217delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78945082 | ||||||
| chr6:78945166
|
A | G | 1 | a0002c0002t0003g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4828+134T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78945166 | ||||||
| chr6:78945760
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.4630+241C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 38/39 | chr6 | 78945760 | ||||||
| chr6:78946308
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4371-48G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/39 | chr6 | 78946308 | ||||||
| chr6:78946926
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4207-52A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78946926 | ||||||
| chr6:78947163
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4207-289G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947163 | ||||||
| chr6:78947230
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4207-356G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947230 | ||||||
| chr6:78947231
|
G | A | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4207-357C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947231 | ||||||
| chr6:78947247
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0005g0107a0001c0001t0039g0083 | 3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.4207-373G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947247 | ||||||
| chr6:78947311
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0119 | 2 | HG02735.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.4206+312C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947311 | ||||||
| chr6:78947325
|
C | T | 72 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0193others(69): Show | 75 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.4206+298G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947325 | ||||||
| chr6:78947602
|
G | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4206+21C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947602 | ||||||
| chr6:78947614
|
ATTAT | A | 10 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(7): Show | 13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.4206+5_4206+8delAT others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947614 | ||||||
| chr6:78947935
|
C | T | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4054-160G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78947935 | ||||||
| chr6:78947951
|
T | TC | 100 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(97): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.4054-177dupG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78947951 | ||||||
| chr6:78948352
|
T | C | 1 | a0003c0003t0002g0284 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4054-577A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948352 | ||||||
| chr6:78948398
|
C | G | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.4054-623G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948398 | ||||||
| chr6:78948412
|
A | C | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4054-637T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948412 | ||||||
| chr6:78948505
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-730G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948505 | ||||||
| chr6:78948588
|
A | G | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4054-813T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948588 | ||||||
| chr6:78948767
|
T | C | 1 | a0001c0005t0038g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4054-992A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948767 | ||||||
| chr6:78948811
|
C | T | 6 | a0004c0004t0006g0007a0004c0004t0006g0008a0004c0004t0006g0180others(3): Show | 8 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.4054-1036G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948811 | ||||||
| chr6:78948818
|
T | C | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.4054-1043A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948818 | ||||||
| chr6:78948841
|
G | GT | 5 | a0001c0001t0059g0118a0001c0005t0023g0049a0001c0005t0023g0051others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4054-1067dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948841 | ||||||
| chr6:78948887
|
C | T | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.4054-1112G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948887 | ||||||
| chr6:78948937
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1162T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948937 | ||||||
| chr6:78949116
|
G | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4054-1341C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949116 | ||||||
| chr6:78949168
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1393C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949168 | ||||||
| chr6:78949174
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1399C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949174 | ||||||
| chr6:78949200
|
T | C | 1 | a0001c0001t0011g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4054-1425A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949200 | ||||||
| chr6:78949315
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0005g0095others(1): Show | 4 | HG00642.hp1 HG02698.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.4054-1540C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949315 | ||||||
| chr6:78949325
|
G | A | 1 | a0002c0002t0008g0200 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4054-1550C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949325 | ||||||
| chr6:78949367
|
A | G | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4054-1592T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949367 | ||||||
| chr6:78949453
|
A | G | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.4054-1678T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949453 | ||||||
| chr6:78949488
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1713C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949488 | ||||||
| chr6:78949662
|
C | T | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4054-1887G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949662 | ||||||
| chr6:78949696
|
T | G | 87 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0001t0001g0131others(84): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.4054-1921A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949696 | ||||||
| chr6:78949696
|
T | TG | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1922_4054-192 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949696 | ||||||
| chr6:78949737
|
A | G | 1 | a0001c0010t0029g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4054-1962T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949737 | ||||||
| chr6:78949950
|
A | G | 1 | a0001c0001t0005g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4054-2175T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949950 | ||||||
| chr6:78950174
|
A | T | 1 | a0001c0001t0005g0077 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4054-2399T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950174 | ||||||
| chr6:78950455
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4054-2680T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950455 | ||||||
| chr6:78950688
|
ATGC | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-2916_4054-291 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950688 | ||||||
| chr6:78950759
|
C | G | 1 | a0001c0001t0005g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4054-2984G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950759 | ||||||
| chr6:78950818
|
ATTG | A | 28 | a0001c0001t0011g0029a0001c0001t0011g0150a0001c0001t0011g0151others(25): Show | 28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4054-3046_4054-304 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950818 | ||||||
| chr6:78950882
|
T | C | 1 | a0002c0002t0003g0243 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4054-3107A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950882 | ||||||
| chr6:78950930
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0105 | 2 | NA18941.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4054-3155G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950930 | ||||||
| chr6:78951018
|
C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4054-3243G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951018 | ||||||
| chr6:78951195
|
G | T | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.4054-3420C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951195 | ||||||
| chr6:78951219
|
T | G | 1 | a0002c0002t0004g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4054-3444A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951219 | ||||||
| chr6:78951235
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-3460A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951235 | ||||||
| chr6:78951336
|
A | T | 2 | a0001c0008t0003g0170a0001c0008t0007g0168 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4053+3478T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951336 | ||||||
| chr6:78951341
|
C | T | 1 | a0002c0002t0004g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4053+3473G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951341 | ||||||
| chr6:78951408
|
T | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.4053+3406A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951408 | ||||||
| chr6:78951434
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+3380A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951434 | ||||||
| chr6:78951464
|
G | A | 6 | a0002c0002t0004g0219a0002c0002t0004g0223a0002c0002t0004g0227others(3): Show | 6 | NA18941.hp2 NA18959.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4053+3350C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951464 | ||||||
| chr6:78951535
|
G | A | 7 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(4): Show | 10 | HG02280.hp1 HG02723.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4053+3279C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951535 | ||||||
| chr6:78951580
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+3234T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951580 | ||||||
| chr6:78951739
|
T | C | 1 | a0001c0005t0030g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4053+3075A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951739 | ||||||
| chr6:78951913
|
T | C | 2 | a0002c0002t0004g0208a0002c0002t0008g0209 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.4053+2901A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951913 | ||||||
| chr6:78951925
|
T | C | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4053+2889A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951925 | ||||||
| chr6:78951948
|
G | C | 5 | a0001c0001t0059g0118a0001c0005t0023g0049a0001c0005t0023g0051others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4053+2866C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951948 | ||||||
| chr6:78951979
|
C | G | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4053+2835G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951979 | ||||||
| chr6:78952009
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4053+2805T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952009 | ||||||
| chr6:78952053
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4053+2761T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952053 | ||||||
| chr6:78952060
|
G | T | 72 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0193others(69): Show | 75 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.4053+2754C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952060 | ||||||
| chr6:78952176
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2638A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952176 | ||||||
| chr6:78952213
|
G | A | 6 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4053+2601C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952213 | ||||||
| chr6:78952312
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2502C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952312 | ||||||
| chr6:78952417
|
CAAAAAAA others(6): Show |
C | 11 | a0001c0001t0014g0160a0001c0001t0015g0156a0001c0001t0015g0159others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.4053+2384_4053+239 others(17): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952417 | ||||||
| chr6:78952426
|
A | G | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4053+2388T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952426 | ||||||
| chr6:78952428
|
G | A | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4053+2386C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952428 | ||||||
| chr6:78952429
|
A | G | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4053+2385T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952429 | ||||||
| chr6:78952611
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2203T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952611 | ||||||
| chr6:78952667
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2147C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952667 | ||||||
| chr6:78952776
|
A | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4053+2038T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952776 | ||||||
| chr6:78952827
|
ACTAT | A | 3 | a0004c0004t0013g0182a0004c0004t0013g0184a0004c0004t0065g0183 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4053+1983_4053+198 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952827 | ||||||
| chr6:78953057
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+1757G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953057 | ||||||
| chr6:78953246
|
G | A | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4053+1568C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953246 | ||||||
| chr6:78953344
|
T | C | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4053+1470A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953344 | ||||||
| chr6:78953352
|
C | A | 96 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.4053+1462G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953352 | ||||||
| chr6:78953391
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+1423A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953391 | ||||||
| chr6:78953488
|
C | A | 14 | a0002c0002t0003g0201a0002c0002t0003g0202a0002c0002t0003g0203others(11): Show | 14 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.4053+1326G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953488 | ||||||
| chr6:78953707
|
C | T | 36 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0268others(33): Show | 42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.4053+1107G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953707 | ||||||
| chr6:78953923
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+891A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953923 | ||||||
| chr6:78954016
|
T | A | 1 | a0001c0006t0002g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4053+798A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954016 | ||||||
| chr6:78954033
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+781A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954033 | ||||||
| chr6:78954157
|
G | A | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4053+657C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954157 | ||||||
| chr6:78954195
|
G | A | 2 | a0001c0001t0026g0149a0001c0001t0026g0154 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4053+619C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954195 | ||||||
| chr6:78954268
|
A | AT | 90 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.4053+545dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954268 | ||||||
| chr6:78954308
|
G | A | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4053+506C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954308 | ||||||
| chr6:78954366
|
A | G | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4053+448T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954366 | ||||||
| chr6:78954401
|
C | T | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.4053+413G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954401 | ||||||
| chr6:78954446
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+368G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954446 | ||||||
| chr6:78954462
|
C | T | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4053+352G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954462 | ||||||
| chr6:78954723
|
T | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.4053+91A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954723 | ||||||
| chr6:78954727
|
CATAAAAA others(52): Show |
C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+28_4053+86del others(59): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954727 | ||||||
| chr6:78954977
|
G | T | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3904-14C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 34/39 | chr6 | 78954977 | ||||||
| chr6:78955031
|
T | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.3904-68A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 34/39 | chr6 | 78955031 | ||||||
| chr6:78955124
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3903+108A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 34/39 | chr6 | 78955124 | ||||||
| chr6:78955350
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3853-68G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955350 | ||||||
| chr6:78955402
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3853-120G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955402 | ||||||
| chr6:78955402
|
C | G | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3853-120G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955402 | ||||||
| chr6:78955442
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3853-160T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955442 | ||||||
| chr6:78955481
|
GT | G | 9 | a0001c0006t0008g0037a0002c0002t0003g0041a0002c0002t0003g0042others(6): Show | 11 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3852+131delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955481 | ||||||
| chr6:78955491
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3852+122A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955491 | ||||||
| chr6:78955493
|
T | A | 133 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.3852+120A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955493 | ||||||
| chr6:78955496
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3852+117T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955496 | ||||||
| chr6:78955513
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3852+100T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955513 | ||||||
| chr6:78955571
|
T | C | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3852+42A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955571 | ||||||
| chr6:78955724
|
GATA | G | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3783-45_3783-43del others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78955724 | ||||||
| chr6:78955860
|
A | G | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3783-178T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78955860 | ||||||
| chr6:78956030
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3783-348A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956030 | ||||||
| chr6:78956076
|
T | C | 1 | a0003c0003t0002g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3783-394A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956076 | ||||||
| chr6:78956148
|
C | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3783-466G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956148 | ||||||
| chr6:78956166
|
G | A | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3783-484C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956166 | ||||||
| chr6:78956170
|
A | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3783-488T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956170 | ||||||
| chr6:78956210
|
C | G | 1 | a0003c0003t0060g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3783-528G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956210 | ||||||
| chr6:78956408
|
A | G | 7 | a0002c0002t0004g0022a0002c0002t0004g0221a0002c0002t0004g0229others(4): Show | 7 | HG02080.hp2 HG02523.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.3783-726T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956408 | ||||||
| chr6:78956492
|
T | G | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3783-810A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956492 | ||||||
| chr6:78956605
|
T | C | 2 | a0002c0002t0048g0020a0002c0002t0053g0194 | 2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3783-923A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956605 | ||||||
| chr6:78956639
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3783-957T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956639 | ||||||
| chr6:78956735
|
C | T | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.3783-1053G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956735 | ||||||
| chr6:78956778
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3783-1096G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956778 | ||||||
| chr6:78956944
|
T | C | 2 | a0001c0007t0012g0174a0001c0007t0012g0175 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3783-1262A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956944 | ||||||
| chr6:78956963
|
A | G | 1 | a0002c0002t0056g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3783-1281T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956963 | ||||||
| chr6:78957159
|
T | C | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+1316A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957159 | ||||||
| chr6:78957579
|
T | TA | 5 | a0001c0001t0001g0134a0001c0005t0019g0012a0001c0005t0019g0264others(2): Show | 6 | HG02723.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+895dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957579 | ||||||
| chr6:78957642
|
C | T | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3782+833G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957642 | ||||||
| chr6:78957645
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3782+830G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957645 | ||||||
| chr6:78957996
|
T | C | 4 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(1): Show | 4 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782+479A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957996 | ||||||
| chr6:78958020
|
T | C | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3782+455A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78958020 | ||||||
| chr6:78958032
|
C | G | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782+443G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78958032 | ||||||
| chr6:78958248
|
C | T | 1 | a0002c0002t0004g0215 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3782+227G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78958248 | ||||||
| chr6:78959086
|
A | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3657-486T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959086 | ||||||
| chr6:78959180
|
A | G | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3657-580T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959180 | ||||||
| chr6:78959194
|
G | T | 1 | a0002c0002t0004g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3657-594C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959194 | ||||||
| chr6:78959211
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0100 | 2 | HG01978.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.3657-611G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959211 | ||||||
| chr6:78959419
|
C | T | 1 | a0007c0018t0001g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3657-819G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959419 | ||||||
| chr6:78959496
|
TA | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3657-897delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959496 | ||||||
| chr6:78959523
|
C | T | 4 | a0002c0002t0003g0010a0002c0002t0003g0244a0002c0002t0003g0245others(1): Show | 5 | HG01074.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.3657-923G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959523 | ||||||
| chr6:78959597
|
T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3657-997A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959597 | ||||||
| chr6:78959818
|
T | G | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.3657-1218A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959818 | ||||||
| chr6:78959842
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3657-1242A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959842 | ||||||
| chr6:78960078
|
T | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3657-1478A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960078 | ||||||
| chr6:78960450
|
C | CT | 8 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(5): Show | 8 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.3656+1239dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960450 | ||||||
| chr6:78960450
|
CT | C | 10 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(7): Show | 10 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3656+1239delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960450 | ||||||
| chr6:78960465
|
T | C | 1 | a0007c0018t0001g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3656+1225A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960465 | ||||||
| chr6:78960484
|
C | A | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3656+1206G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960484 | ||||||
| chr6:78960507
|
G | A | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3656+1183C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960507 | ||||||
| chr6:78960642
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3656+1048C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960642 | ||||||
| chr6:78960895
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3656+795A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960895 | ||||||
| chr6:78960914
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3656+776C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960914 | ||||||
| chr6:78960948
|
A | G | 1 | a0001c0005t0019g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3656+742T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960948 | ||||||
| chr6:78961242
|
T | C | 1 | a0002c0009t0004g0214 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3656+448A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961242 | ||||||
| chr6:78961256
|
C | T | 284 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(281): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.3656+434G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961256 | ||||||
| chr6:78961285
|
C | T | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3656+405G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961285 | ||||||
| chr6:78961366
|
C | T | 2 | a0002c0002t0003g0201a0002c0002t0003g0202 | 2 | NA18974.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3656+324G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961366 | ||||||
| chr6:78961383
|
A | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3656+307T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961383 | ||||||
| chr6:78961428
|
G | A | 7 | a0004c0004t0006g0007a0004c0004t0006g0008a0004c0004t0006g0180others(4): Show | 9 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.3656+262C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961428 | ||||||
| chr6:78961635
|
G | C | 15 | a0002c0002t0003g0201a0002c0002t0003g0202a0002c0002t0003g0203others(12): Show | 15 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.3656+55C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961635 | ||||||
| chr6:78961914
|
C | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3536-104G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78961914 | ||||||
| chr6:78962016
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3536-206A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962016 | ||||||
| chr6:78962028
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3536-218A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962028 | ||||||
| chr6:78962196
|
C | G | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.3536-386G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962196 | ||||||
| chr6:78962416
|
G | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.3536-606C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962416 | ||||||
| chr6:78962502
|
CTCT | C | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3535+592_3535+594d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962502 | ||||||
| chr6:78962578
|
C | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3535+519G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962578 | ||||||
| chr6:78962586
|
A | C | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3535+511T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962586 | ||||||
| chr6:78962630
|
G | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3535+467C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962630 | ||||||
| chr6:78962721
|
T | C | 96 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3535+376A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962721 | ||||||
| chr6:78962805
|
A | G | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.3535+292T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962805 | ||||||
| chr6:78962928
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3535+169A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962928 | ||||||
| chr6:78963064
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3535+33C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78963064 | ||||||
| chr6:78963287
|
G | A | 1 | a0001c0001t0005g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3380-35C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963287 | ||||||
| chr6:78963576
|
C | T | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3380-324G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963576 | ||||||
| chr6:78963796
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-544C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963796 | ||||||
| chr6:78963816
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-564G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963816 | ||||||
| chr6:78963954
|
GAAC | G | 11 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(8): Show | 12 | HG00738.hp1 HG01106.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3380-705_3380-703d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963954 | ||||||
| chr6:78963973
|
C | T | 1 | a0003c0003t0002g0279 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3380-721G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963973 | ||||||
| chr6:78964024
|
C | A | 1 | a0002c0002t0066g0230 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3380-772G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964024 | ||||||
| chr6:78964070
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-818G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964070 | ||||||
| chr6:78964148
|
A | G | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3380-896T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964148 | ||||||
| chr6:78964171
|
A | G | 1 | a0001c0001t0025g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3380-919T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964171 | ||||||
| chr6:78964176
|
A | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3380-924T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964176 | ||||||
| chr6:78964225
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-973T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964225 | ||||||
| chr6:78964355
|
T | C | 1 | a0002c0002t0004g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3380-1103A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964355 | ||||||
| chr6:78964459
|
G | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.3380-1207C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964459 | ||||||
| chr6:78964545
|
C | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.3379+1158G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964545 | ||||||
| chr6:78964692
|
C | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3379+1011G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964692 | ||||||
| chr6:78964700
|
T | C | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3379+1003A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964700 | ||||||
| chr6:78964706
|
T | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3379+997A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964706 | ||||||
| chr6:78964716
|
C | T | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3379+987G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964716 | ||||||
| chr6:78964721
|
G | A | 7 | a0004c0004t0006g0007a0004c0004t0006g0008a0004c0004t0006g0180others(4): Show | 9 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.3379+982C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964721 | ||||||
| chr6:78964808
|
T | C | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3379+895A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964808 | ||||||
| chr6:78964916
|
T | A | 1 | a0001c0006t0009g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3379+787A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964916 | ||||||
| chr6:78964993
|
T | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3379+710A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964993 | ||||||
| chr6:78965103
|
GAC | G | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379+598_3379+599d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965103 | ||||||
| chr6:78965139
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3379+564A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965139 | ||||||
| chr6:78965212
|
T | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(97): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.3379+491A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965212 | ||||||
| chr6:78965552
|
ACTT | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3379+148_3379+150d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965552 | ||||||
| chr6:78965558
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3379+145T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965558 | ||||||
| chr6:78965910
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3317+35G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 28/39 | chr6 | 78965910 | ||||||
| chr6:78966228
|
A | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3206-172T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966228 | ||||||
| chr6:78966230
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-174C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966230 | ||||||
| chr6:78966231
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-175T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966231 | ||||||
| chr6:78966322
|
G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3206-266C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966322 | ||||||
| chr6:78966345
|
G | A | 96 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3206-289C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966345 | ||||||
| chr6:78966539
|
A | G | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3206-483T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966539 | ||||||
| chr6:78966611
|
A | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.3206-555T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966611 | ||||||
| chr6:78966711
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-655T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966711 | ||||||
| chr6:78966728
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3206-672A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966728 | ||||||
| chr6:78966741
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-685T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966741 | ||||||
| chr6:78966862
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.3206-806G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966862 | ||||||
| chr6:78966895
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-839T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966895 | ||||||
| chr6:78966996
|
A | G | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3206-940T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966996 | ||||||
| chr6:78967328
|
AC | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-1273delG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967328 | ||||||
| chr6:78967483
|
C | T | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3206-1427G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967483 | ||||||
| chr6:78967533
|
C | T | 2 | a0001c0001t0005g0107a0001c0001t0033g0021 | 2 | HG00280.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.3206-1477G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967533 | ||||||
| chr6:78967534
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-1478C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967534 | ||||||
| chr6:78967653
|
T | C | 1 | a0001c0001t0040g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3206-1597A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967653 | ||||||
| chr6:78967927
|
G | A | 5 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0050others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3206-1871C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967927 | ||||||
| chr6:78967963
|
T | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3205+1872A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967963 | ||||||
| chr6:78967969
|
C | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3205+1866G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967969 | ||||||
| chr6:78968072
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+1763A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968072 | ||||||
| chr6:78968122
|
G | A | 1 | a0003c0003t0002g0032 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3205+1713C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968122 | ||||||
| chr6:78968214
|
T | C | 2 | a0001c0001t0026g0149a0001c0001t0026g0154 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3205+1621A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968214 | ||||||
| chr6:78968239
|
C | T | 2 | a0004c0004t0013g0182a0004c0004t0065g0183 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3205+1596G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968239 | ||||||
| chr6:78968254
|
CT | C | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3205+1580delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968254 | ||||||
| chr6:78968379
|
T | C | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205+1456A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968379 | ||||||
| chr6:78968405
|
G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3205+1430C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968405 | ||||||
| chr6:78968446
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+1389C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968446 | ||||||
| chr6:78968494
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.3205+1341C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968494 | ||||||
| chr6:78968550
|
G | A | 1 | a0001c0001t0005g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3205+1285C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968550 | ||||||
| chr6:78968610
|
A | G | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3205+1225T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968610 | ||||||
| chr6:78968613
|
A | G | 1 | a0003c0003t0002g0295 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3205+1222T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968613 | ||||||
| chr6:78968667
|
A | C | 5 | a0002c0002t0003g0201a0002c0002t0003g0202a0002c0002t0003g0203others(2): Show | 5 | NA18945.hp2 NA18974.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.3205+1168T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968667 | ||||||
| chr6:78968731
|
AAATT | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.3205+1100_3205+110 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968731 | ||||||
| chr6:78968952
|
T | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3205+883A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968952 | ||||||
| chr6:78968960
|
A | G | 1 | a0001c0001t0021g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3205+875T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968960 | ||||||
| chr6:78969089
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3205+746A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969089 | ||||||
| chr6:78969242
|
C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3205+593G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969242 | ||||||
| chr6:78969282
|
C | T | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3205+553G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969282 | ||||||
| chr6:78969376
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3205+459A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969376 | ||||||
| chr6:78969403
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3205+432G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969403 | ||||||
| chr6:78969404
|
A | T | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3205+431T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969404 | ||||||
| chr6:78969406
|
A | C | 1 | a0003c0003t0002g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3205+429T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969406 | ||||||
| chr6:78969646
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+189C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969646 | ||||||
| chr6:78969810
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+25C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969810 | ||||||
| chr6:78970043
|
C | T | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3122+6G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 26/39 | chr6 | 78970043 | ||||||
| chr6:78970287
|
G | T | 1 | a0001c0001t0034g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2998-114C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970287 | ||||||
| chr6:78970346
|
T | C | 28 | a0001c0001t0011g0029a0001c0001t0011g0150a0001c0001t0011g0151others(25): Show | 28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.2998-173A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970346 | ||||||
| chr6:78970352
|
T | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2998-179A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970352 | ||||||
| chr6:78970506
|
G | A | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2997+275C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970506 | ||||||
| chr6:78970581
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2997+200A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970581 | ||||||
| chr6:78970703
|
T | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2997+78A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970703 | ||||||
| chr6:78970989
|
C | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-101G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78970989 | ||||||
| chr6:78971040
|
C | G | 3 | a0003c0003t0002g0292a0003c0003t0009g0016a0003c0003t0052g0298 | 4 | HG00438.hp2 HG02155.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.2890-152G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971040 | ||||||
| chr6:78971047
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2890-159A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971047 | ||||||
| chr6:78971134
|
C | A | 1 | a0001c0006t0002g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2890-246G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971134 | ||||||
| chr6:78971274
|
C | A | 1 | a0001c0011t0016g0018 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2890-386G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971274 | ||||||
| chr6:78971475
|
C | T | 2 | a0002c0002t0004g0208a0002c0002t0008g0209 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2890-587G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971475 | ||||||
| chr6:78971516
|
G | A | 1 | a0001c0005t0038g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2890-628C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971516 | ||||||
| chr6:78971652
|
C | T | 96 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2890-764G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971652 | ||||||
| chr6:78971658
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-770A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971658 | ||||||
| chr6:78971663
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-775C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971663 | ||||||
| chr6:78971668
|
C | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2890-780G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971668 | ||||||
| chr6:78971670
|
C | T | 2 | a0001c0001t0001g0129a0001c0006t0008g0037 | 2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2890-782G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971670 | ||||||
| chr6:78971671
|
G | A | 96 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2890-783C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971671 | ||||||
| chr6:78971678
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2890-790C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971678 | ||||||
| chr6:78971679
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2890-791A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971679 | ||||||
| chr6:78971682
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2890-794C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971682 | ||||||
| chr6:78971766
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-878G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971766 | ||||||
| chr6:78971809
|
C | T | 1 | a0003c0003t0002g0274 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2890-921G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971809 | ||||||
| chr6:78971833
|
C | A | 1 | a0004c0004t0006g0188 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2890-945G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971833 | ||||||
| chr6:78971843
|
C | T | 3 | a0001c0006t0002g0265a0001c0006t0009g0266a0001c0006t0009g0297 | 3 | HG01891.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2890-955G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971843 | ||||||
| chr6:78971844
|
G | A | 2 | a0002c0002t0010g0206a0002c0002t0010g0234 | 2 | HG02080.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2890-956C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971844 | ||||||
| chr6:78971857
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-969C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971857 | ||||||
| chr6:78971872
|
G | T | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2890-984C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971872 | ||||||
| chr6:78971884
|
C | T | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2890-996G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971884 | ||||||
| chr6:78971933
|
C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1045G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971933 | ||||||
| chr6:78971934
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2890-1046C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971934 | ||||||
| chr6:78971997
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1109G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971997 | ||||||
| chr6:78971998
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0040g0079 | 3 | HG00642.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2890-1110C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971998 | ||||||
| chr6:78972007
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1119C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972007 | ||||||
| chr6:78972164
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1276A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972164 | ||||||
| chr6:78972166
|
C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1278G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972166 | ||||||
| chr6:78972168
|
C | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1280G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972168 | ||||||
| chr6:78972221
|
C | T | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2890-1333G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972221 | ||||||
| chr6:78972292
|
C | T | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2890-1404G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972292 | ||||||
| chr6:78972330
|
A | C | 9 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0086others(6): Show | 9 | HG00673.hp1 HG02165.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.2890-1442T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972330 | ||||||
| chr6:78972470
|
C | T | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2890-1582G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972470 | ||||||
| chr6:78972519
|
C | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2890-1631G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972519 | ||||||
| chr6:78972566
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2890-1678C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972566 | ||||||
| chr6:78972566
|
G | T | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2890-1678C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972566 | ||||||
| chr6:78972587
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1699T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972587 | ||||||
| chr6:78972609
|
C | G | 5 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG00673.hp1 NA18943.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2890-1721G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972609 | ||||||
| chr6:78972649
|
G | A | 3 | a0004c0004t0013g0182a0004c0004t0013g0184a0004c0004t0065g0183 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2890-1761C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972649 | ||||||
| chr6:78972649
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1761C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972649 | ||||||
| chr6:78972650
|
T | C | 86 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(83): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2890-1762A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972650 | ||||||
| chr6:78972692
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1804A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972692 | ||||||
| chr6:78972721
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1833A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972721 | ||||||
| chr6:78972754
|
G | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2890-1866C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972754 | ||||||
| chr6:78972757
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2890-1869C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972757 | ||||||
| chr6:78972780
|
A | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2890-1892T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972780 | ||||||
| chr6:78972789
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1901A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972789 | ||||||
| chr6:78972804
|
G | T | 1 | a0004c0004t0006g0181 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2890-1916C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972804 | ||||||
| chr6:78972808
|
C | T | 1 | a0001c0001t0014g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2890-1920G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972808 | ||||||
| chr6:78972823
|
A | G | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2890-1935T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972823 | ||||||
| chr6:78972848
|
G | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2890-1960C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972848 | ||||||
| chr6:78972850
|
G | A | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2890-1962C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972850 | ||||||
| chr6:78972897
|
G | A | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2890-2009C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972897 | ||||||
| chr6:78972903
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2015A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972903 | ||||||
| chr6:78972950
|
A | ACT | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2064_2890-206 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972950 | ||||||
| chr6:78972980
|
CA | C | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2890-2093delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972980 | ||||||
| chr6:78973150
|
G | T | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2890-2262C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973150 | ||||||
| chr6:78973171
|
C | T | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2890-2283G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973171 | ||||||
| chr6:78973181
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2293T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973181 | ||||||
| chr6:78973206
|
G | A | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2890-2318C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973206 | ||||||
| chr6:78973306
|
A | C | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2890-2418T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973306 | ||||||
| chr6:78973315
|
A | G | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2890-2427T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973315 | ||||||
| chr6:78973359
|
C | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2890-2471G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973359 | ||||||
| chr6:78973378
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2490G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973378 | ||||||
| chr6:78973412
|
G | A | 81 | a0001c0010t0057g0163a0002c0002t0003g0010a0002c0002t0003g0011others(78): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2890-2524C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973412 | ||||||
| chr6:78973430
|
A | C | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2890-2542T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973430 | ||||||
| chr6:78973443
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2555A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973443 | ||||||
| chr6:78973473
|
T | C | 283 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(280): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2890-2585A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973473 | ||||||
| chr6:78973474
|
G | A | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2890-2586C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973474 | ||||||
| chr6:78973544
|
C | A | 297 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(294): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2890-2656G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973544 | ||||||
| chr6:78973548
|
G | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2890-2660C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973548 | ||||||
| chr6:78973557
|
T | G | 297 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(294): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2890-2669A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973557 | ||||||
| chr6:78973586
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(293): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2890-2698A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973586 | ||||||
| chr6:78973595
|
C | G | 297 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(294): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2890-2707G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973595 | ||||||
| chr6:78973624
|
A | G | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2890-2736T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973624 | ||||||
| chr6:78973640
|
C | G | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2890-2752G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973640 | ||||||
| chr6:78973696
|
A | C | 1 | a0003c0003t0061g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2890-2808T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973696 | ||||||
| chr6:78973778
|
A | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2890-2890T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973778 | ||||||
| chr6:78973945
|
C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-3057G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973945 | ||||||
| chr6:78973980
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3092A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973980 | ||||||
| chr6:78973983
|
C | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3095G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973983 | ||||||
| chr6:78974030
|
T | C | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2890-3142A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974030 | ||||||
| chr6:78974070
|
T | C | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2890-3182A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974070 | ||||||
| chr6:78974107
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3219T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974107 | ||||||
| chr6:78974119
|
C | G | 3 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0044 | 3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2890-3231G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974119 | ||||||
| chr6:78974119
|
C | T | 1 | a0001c0001t0021g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2890-3231G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974119 | ||||||
| chr6:78974174
|
A | G | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2890-3286T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974174 | ||||||
| chr6:78974190
|
A | T | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2890-3302T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974190 | ||||||
| chr6:78974280
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2890-3392C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974280 | ||||||
| chr6:78974296
|
A | G | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2890-3408T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974296 | ||||||
| chr6:78974330
|
A | G | 1 | a0001c0001t0035g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2890-3442T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974330 | ||||||
| chr6:78974365
|
G | A | 2 | a0001c0001t0026g0149a0001c0001t0026g0154 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2890-3477C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974365 | ||||||
| chr6:78974391
|
A | G | 1 | a0002c0014t0003g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2890-3503T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974391 | ||||||
| chr6:78974418
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3530A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974418 | ||||||
| chr6:78974445
|
C | T | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2890-3557G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974445 | ||||||
| chr6:78974521
|
A | C | 9 | a0001c0001t0014g0158a0001c0001t0014g0160a0001c0001t0014g0161others(6): Show | 9 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2890-3633T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974521 | ||||||
| chr6:78974621
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3733T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974621 | ||||||
| chr6:78974623
|
C | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2890-3735G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974623 | ||||||
| chr6:78974700
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2890-3812C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974700 | ||||||
| chr6:78974728
|
G | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2890-3840C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974728 | ||||||
| chr6:78974856
|
A | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2889+3736T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974856 | ||||||
| chr6:78974985
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+3607A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974985 | ||||||
| chr6:78975014
|
C | G | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2889+3578G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975014 | ||||||
| chr6:78975052
|
T | C | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2889+3540A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975052 | ||||||
| chr6:78975068
|
C | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2889+3524G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975068 | ||||||
| chr6:78975077
|
T | G | 3 | a0001c0005t0003g0001a0001c0010t0029g0053a0001c0010t0029g0054 | 5 | HG02280.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+3515A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975077 | ||||||
| chr6:78975142
|
G | A | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2889+3450C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975142 | ||||||
| chr6:78975164
|
G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2889+3428C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975164 | ||||||
| chr6:78975223
|
G | A | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2889+3369C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975223 | ||||||
| chr6:78975259
|
C | G | 2 | a0002c0002t0004g0208a0002c0002t0008g0209 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2889+3333G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975259 | ||||||
| chr6:78975316
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+3276T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975316 | ||||||
| chr6:78975364
|
G | T | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2889+3228C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975364 | ||||||
| chr6:78975398
|
C | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2889+3194G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975398 | ||||||
| chr6:78975505
|
T | G | 1 | a0003c0003t0002g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2889+3087A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975505 | ||||||
| chr6:78975530
|
TAGGC | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+3058_2889+306 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975530 | ||||||
| chr6:78975606
|
A | G | 1 | a0002c0002t0003g0201 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2889+2986T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975606 | ||||||
| chr6:78975732
|
G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2889+2860C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975732 | ||||||
| chr6:78975741
|
G | A | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2889+2851C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975741 | ||||||
| chr6:78975774
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0110 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2889+2818T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975774 | ||||||
| chr6:78975821
|
T | C | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2889+2771A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975821 | ||||||
| chr6:78975832
|
T | C | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2889+2760A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975832 | ||||||
| chr6:78975887
|
A | T | 28 | a0001c0001t0011g0029a0001c0001t0011g0150a0001c0001t0011g0151others(25): Show | 28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.2889+2705T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975887 | ||||||
| chr6:78975932
|
G | T | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2889+2660C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975932 | ||||||
| chr6:78975977
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2615G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975977 | ||||||
| chr6:78976060
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2532A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976060 | ||||||
| chr6:78976100
|
C | A | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+2492G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976100 | ||||||
| chr6:78976164
|
G | T | 4 | a0001c0001t0005g0098a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 5 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2889+2428C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976164 | ||||||
| chr6:78976166
|
C | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+2426G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976166 | ||||||
| chr6:78976172
|
C | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+2420G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976172 | ||||||
| chr6:78976219
|
C | T | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2889+2373G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976219 | ||||||
| chr6:78976256
|
GA | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(93): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.2889+2335delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976256 | ||||||
| chr6:78976426
|
A | G | 3 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0044 | 3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2889+2166T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976426 | ||||||
| chr6:78976428
|
G | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2889+2164C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976428 | ||||||
| chr6:78976436
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2156T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976436 | ||||||
| chr6:78976455
|
A | G | 274 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(271): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2889+2137T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976455 | ||||||
| chr6:78976488
|
A | C | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2889+2104T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976488 | ||||||
| chr6:78976494
|
G | A | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2889+2098C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976494 | ||||||
| chr6:78976559
|
A | G | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+2033T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976559 | ||||||
| chr6:78976580
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2012C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976580 | ||||||
| chr6:78976597
|
A | C | 1 | a0001c0001t0011g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2889+1995T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976597 | ||||||
| chr6:78976614
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2889+1978C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976614 | ||||||
| chr6:78976618
|
T | C | 4 | a0001c0006t0002g0271a0001c0011t0016g0017a0001c0011t0016g0018others(1): Show | 4 | HG01123.hp1 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+1974A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976618 | ||||||
| chr6:78976644
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1948A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976644 | ||||||
| chr6:78976718
|
C | T | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2889+1874G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976718 | ||||||
| chr6:78976791
|
C | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1801G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976791 | ||||||
| chr6:78976845
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1747T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976845 | ||||||
| chr6:78976874
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1718G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976874 | ||||||
| chr6:78976940
|
A | G | 1 | a0004c0004t0013g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2889+1652T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976940 | ||||||
| chr6:78976941
|
A | G | 282 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(279): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2889+1651T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976941 | ||||||
| chr6:78976980
|
G | T | 124 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(121): Show | 125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2889+1612C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976980 | ||||||
| chr6:78977024
|
G | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+1568C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977024 | ||||||
| chr6:78977089
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1503A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977089 | ||||||
| chr6:78977136
|
A | T | 1 | a0004c0004t0013g0166 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2889+1456T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977136 | ||||||
| chr6:78977147
|
C | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(274): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2889+1445G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977147 | ||||||
| chr6:78977318
|
T | C | 3 | a0001c0001t0021g0027a0001c0001t0021g0028a0001c0001t0021g0030 | 3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2889+1274A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977318 | ||||||
| chr6:78977389
|
G | A | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2889+1203C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977389 | ||||||
| chr6:78977472
|
G | A | 3 | a0001c0001t0011g0151a0001c0001t0018g0152a0001c0005t0003g0001 | 5 | HG02055.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+1120C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977472 | ||||||
| chr6:78977513
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1079G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977513 | ||||||
| chr6:78977521
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1071T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977521 | ||||||
| chr6:78977530
|
C | A | 1 | a0001c0001t0032g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2889+1062G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977530 | ||||||
| chr6:78977587
|
G | GACCTTCA others(3): Show |
132 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(129): Show | 133 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2889+995_2889+1004 others(13): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977587 | ||||||
| chr6:78977628
|
T | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2889+964A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977628 | ||||||
| chr6:78977629
|
T | G | 4 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(1): Show | 4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+963A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977629 | ||||||
| chr6:78977677
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0001t0001g0131 | 3 | HG00140.hp1 HG01175.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2889+915C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977677 | ||||||
| chr6:78977705
|
T | C | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+887A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977705 | ||||||
| chr6:78977760
|
T | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2889+832A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977760 | ||||||
| chr6:78977867
|
T | C | 1 | a0002c0002t0010g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2889+725A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977867 | ||||||
| chr6:78977999
|
G | A | 2 | a0003c0003t0002g0278a0003c0003t0009g0277 | 2 | NA18950.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2889+593C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977999 | ||||||
| chr6:78978200
|
C | G | 1 | a0002c0002t0028g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2889+392G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978200 | ||||||
| chr6:78978259
|
A | C | 6 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2889+333T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978259 | ||||||
| chr6:78978262
|
A | G | 1 | a0001c0005t0023g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2889+330T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978262 | ||||||
| chr6:78978334
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+258T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978334 | ||||||
| chr6:78978373
|
C | G | 4 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(1): Show | 4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+219G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978373 | ||||||
| chr6:78978431
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+161G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978431 | ||||||
| chr6:78978460
|
C | T | 1 | a0001c0005t0045g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2889+132G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978460 | ||||||
| chr6:78978462
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+130A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978462 | ||||||
| chr6:78978823
|
T | C | 3 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0044 | 3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2770-112A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78978823 | ||||||
| chr6:78978914
|
A | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2770-203T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78978914 | ||||||
| chr6:78978915
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2770-204T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78978915 | ||||||
| chr6:78979036
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-325G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979036 | ||||||
| chr6:78979045
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2770-334A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979045 | ||||||
| chr6:78979115
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-404C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979115 | ||||||
| chr6:78979613
|
G | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2770-902C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979613 | ||||||
| chr6:78979733
|
C | T | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.2770-1022G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979733 | ||||||
| chr6:78979753
|
T | G | 1 | a0001c0001t0005g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2770-1042A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979753 | ||||||
| chr6:78979778
|
CTTGT | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-1071_2770-106 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979778 | ||||||
| chr6:78979786
|
T | C | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2770-1075A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979786 | ||||||
| chr6:78979950
|
C | T | 1 | a0001c0011t0016g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2770-1239G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979950 | ||||||
| chr6:78980251
|
G | GA | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2770-1541dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980251 | ||||||
| chr6:78980330
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-1619T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980330 | ||||||
| chr6:78980442
|
C | A | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2770-1731G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980442 | ||||||
| chr6:78980573
|
G | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.2770-1862C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980573 | ||||||
| chr6:78980710
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2770-1999G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980710 | ||||||
| chr6:78980859
|
C | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2769+2027G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980859 | ||||||
| chr6:78980935
|
A | T | 1 | a0001c0005t0030g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2769+1951T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980935 | ||||||
| chr6:78981151
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+1735A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981151 | ||||||
| chr6:78981186
|
A | C | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2769+1700T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981186 | ||||||
| chr6:78981187
|
G | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2769+1699C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981187 | ||||||
| chr6:78981367
|
C | T | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2769+1519G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981367 | ||||||
| chr6:78981381
|
C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2769+1505G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981381 | ||||||
| chr6:78981440
|
A | G | 1 | a0002c0002t0010g0222 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2769+1446T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981440 | ||||||
| chr6:78981458
|
A | G | 36 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0268others(33): Show | 42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2769+1428T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981458 | ||||||
| chr6:78981525
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+1361C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981525 | ||||||
| chr6:78981676
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0141a0001c0001t0005g0140others(1): Show | 5 | HG02257.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2769+1210G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981676 | ||||||
| chr6:78981857
|
T | C | 1 | a0001c0001t0005g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2769+1029A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981857 | ||||||
| chr6:78982002
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2769+884A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982002 | ||||||
| chr6:78982015
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+871A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982015 | ||||||
| chr6:78982029
|
G | A | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2769+857C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982029 | ||||||
| chr6:78982249
|
A | G | 3 | a0001c0010t0029g0053a0001c0010t0029g0054a0002c0002t0010g0224 | 3 | HG00558.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2769+637T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982249 | ||||||
| chr6:78982372
|
A | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2769+514T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982372 | ||||||
| chr6:78982459
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+427C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982459 | ||||||
| chr6:78982481
|
T | C | 1 | a0001c0010t0029g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2769+405A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982481 | ||||||
| chr6:78982682
|
A | C | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2769+204T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982682 | ||||||
| chr6:78982731
|
T | G | 1 | a0002c0002t0004g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2769+155A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982731 | ||||||
| chr6:78983377
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2538-260G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983377 | ||||||
| chr6:78983745
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2538-628C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983745 | ||||||
| chr6:78983902
|
T | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2538-785A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983902 | ||||||
| chr6:78983939
|
G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2538-822C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983939 | ||||||
| chr6:78983946
|
TTTAC | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2538-833_2538-830d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983946 | ||||||
| chr6:78984193
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2538-1076T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984193 | ||||||
| chr6:78984235
|
T | C | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2537+1117A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984235 | ||||||
| chr6:78984252
|
G | C | 3 | a0001c0001t0001g0082a0001c0001t0005g0107a0001c0001t0039g0083 | 3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2537+1100C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984252 | ||||||
| chr6:78984391
|
C | CT | 4 | a0003c0003t0002g0015a0003c0003t0002g0286a0003c0003t0009g0276others(1): Show | 5 | HG00099.hp2 HG01070.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2537+960_2537+961i others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984391 | ||||||
| chr6:78984418
|
A | AGT | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2537+932_2537+933d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984418 | ||||||
| chr6:78984442
|
T | A | 1 | a0001c0010t0029g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2537+910A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984442 | ||||||
| chr6:78984498
|
C | T | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2537+854G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984498 | ||||||
| chr6:78984617
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2537+735C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984617 | ||||||
| chr6:78984753
|
T | C | 2 | a0004c0004t0013g0182a0004c0004t0065g0183 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2537+599A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984753 | ||||||
| chr6:78984759
|
G | C | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2537+593C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984759 | ||||||
| chr6:78984769
|
A | G | 2 | a0001c0001t0014g0160a0001c0001t0015g0159 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2537+583T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984769 | ||||||
| chr6:78984882
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0146a0001c0001t0005g0145 | 3 | NA18612.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2537+470A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984882 | ||||||
| chr6:78984932
|
C | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2537+420G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984932 | ||||||
| chr6:78985012
|
A | G | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2537+340T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985012 | ||||||
| chr6:78985014
|
GA | G | 6 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0197others(3): Show | 6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2537+337delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985014 | ||||||
| chr6:78985016
|
T | G | 6 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0197others(3): Show | 6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2537+336A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985016 | ||||||
| chr6:78985019
|
TTAACTCA | T | 6 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0197others(3): Show | 6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2537+326_2537+332d others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985019 | ||||||
| chr6:78985087
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2537+265G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985087 | ||||||
| chr6:78985099
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0105 | 2 | NA18941.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2537+253T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985099 | ||||||
| chr6:78985286
|
T | TA | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2537+65dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985286 | ||||||
| chr6:78985312
|
C | T | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.2537+40G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985312 | ||||||
| chr6:78985569
|
T | C | 1 | a0002c0002t0022g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2461-141A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985569 | ||||||
| chr6:78985607
|
A | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2461-179T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985607 | ||||||
| chr6:78985614
|
G | A | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2461-186C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985614 | ||||||
| chr6:78985656
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2461-228G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985656 | ||||||
| chr6:78985746
|
G | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2461-318C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985746 | ||||||
| chr6:78985751
|
G | A | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2461-323C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985751 | ||||||
| chr6:78986314
|
T | C | 1 | a0001c0001t0005g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2461-886A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986314 | ||||||
| chr6:78986398
|
T | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2461-970A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986398 | ||||||
| chr6:78986481
|
T | C | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2461-1053A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986481 | ||||||
| chr6:78986552
|
C | T | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2461-1124G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986552 | ||||||
| chr6:78986756
|
T | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2461-1328A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986756 | ||||||
| chr6:78986948
|
GAAT | G | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2460+1258_2460+126 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986948 | ||||||
| chr6:78986957
|
C | A | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460+1252G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986957 | ||||||
| chr6:78986986
|
C | T | 1 | a0003c0003t0002g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2460+1223G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986986 | ||||||
| chr6:78987089
|
A | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460+1120T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987089 | ||||||
| chr6:78987222
|
A | G | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2460+987T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987222 | ||||||
| chr6:78987313
|
T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2460+896A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987313 | ||||||
| chr6:78987468
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2460+741A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987468 | ||||||
| chr6:78987594
|
A | G | 1 | a0001c0007t0012g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2460+615T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987594 | ||||||
| chr6:78987732
|
A | C | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2460+477T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987732 | ||||||
| chr6:78987960
|
G | C | 2 | a0001c0001t0059g0118a0001c0010t0057g0163 | 2 | HG01358.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2460+249C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987960 | ||||||
| chr6:78988138
|
G | A | 10 | a0004c0004t0006g0007a0004c0004t0006g0008a0004c0004t0006g0180others(7): Show | 12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2460+71C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78988138 | ||||||
| chr6:78988155
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2460+54A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78988155 | ||||||
| chr6:78988479
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2320-130A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988479 | ||||||
| chr6:78988528
|
T | A | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2320-179A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988528 | ||||||
| chr6:78988528
|
T | C | 1 | a0001c0006t0002g0014 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2320-179A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988528 | ||||||
| chr6:78988663
|
C | T | 128 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.2320-314G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988663 | ||||||
| chr6:78988665
|
T | C | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2320-316A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988665 | ||||||
| chr6:78988698
|
G | A | 6 | a0001c0005t0030g0048a0001c0008t0003g0170a0001c0008t0007g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2320-349C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988698 | ||||||
| chr6:78988699
|
A | T | 6 | a0001c0005t0030g0048a0001c0008t0003g0170a0001c0008t0007g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2320-350T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988699 | ||||||
| chr6:78988735
|
GT | G | 59 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0005g0116others(56): Show | 65 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2320-387delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988735 | ||||||
| chr6:78988748
|
C | T | 1 | a0001c0001t0005g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2320-399G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988748 | ||||||
| chr6:78988806
|
T | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2320-457A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988806 | ||||||
| chr6:78988928
|
A | C | 4 | a0002c0002t0003g0010a0002c0002t0003g0244a0002c0002t0003g0245others(1): Show | 5 | HG01074.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-579T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988928 | ||||||
| chr6:78989083
|
C | T | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2320-734G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989083 | ||||||
| chr6:78989094
|
C | CA | 128 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.2320-746dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989094 | ||||||
| chr6:78989220
|
C | A | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2320-871G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989220 | ||||||
| chr6:78989228
|
G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2320-879C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989228 | ||||||
| chr6:78989430
|
C | T | 1 | a0002c0002t0022g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2320-1081G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989430 | ||||||
| chr6:78989632
|
T | C | 4 | a0001c0001t0011g0029a0001c0001t0021g0027a0001c0001t0021g0028others(1): Show | 4 | HG02922.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+1236A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989632 | ||||||
| chr6:78989640
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2319+1228G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989640 | ||||||
| chr6:78989689
|
G | C | 8 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0003others(5): Show | 10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2319+1179C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989689 | ||||||
| chr6:78989802
|
T | C | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2319+1066A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989802 | ||||||
| chr6:78990044
|
GAGA | G | 7 | a0001c0005t0030g0048a0001c0008t0003g0170a0001c0008t0007g0167others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2319+821_2319+823d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990044 | ||||||
| chr6:78990120
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2319+748G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990120 | ||||||
| chr6:78990190
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2319+678T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990190 | ||||||
| chr6:78990321
|
G | A | 274 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(271): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2319+547C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990321 | ||||||
| chr6:78990440
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2319+428A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990440 | ||||||
| chr6:78990442
|
A | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2319+426T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990442 | ||||||
| chr6:78990472
|
A | G | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+396T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990472 | ||||||
| chr6:78990608
|
G | C | 96 | a0001c0005t0030g0048a0001c0007t0012g0172a0001c0007t0012g0173others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2319+260C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990608 | ||||||
| chr6:78990635
|
A | C | 1 | a0002c0002t0004g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2319+233T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990635 | ||||||
| chr6:78990721
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2319+147A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990721 | ||||||
| chr6:78991013
|
T | A | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2202-28A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991013 | ||||||
| chr6:78991121
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-136T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991121 | ||||||
| chr6:78991147
|
C | G | 1 | a0001c0005t0019g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2202-162G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991147 | ||||||
| chr6:78991149
|
G | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2202-164C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991149 | ||||||
| chr6:78991156
|
C | T | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2202-171G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991156 | ||||||
| chr6:78991263
|
T | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.2202-278A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991263 | ||||||
| chr6:78991302
|
T | A | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2202-317A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991302 | ||||||
| chr6:78991352
|
CTGT | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2202-370_2202-368d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991352 | ||||||
| chr6:78991392
|
T | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2202-407A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991392 | ||||||
| chr6:78991442
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0110 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2202-457A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991442 | ||||||
| chr6:78991560
|
G | GAGA | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-578_2202-576d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991560 | ||||||
| chr6:78991615
|
T | C | 5 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0050others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2202-630A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991615 | ||||||
| chr6:78991853
|
AT | A | 33 | a0001c0001t0001g0096a0001c0001t0001g0110a0001c0001t0011g0029others(30): Show | 36 | HG01109.hp2 HG01358.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.2202-869delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991853 | ||||||
| chr6:78991854
|
T | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2202-869A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991854 | ||||||
| chr6:78991865
|
T | A | 2 | a0001c0011t0016g0017a0001c0011t0016g0018 | 2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2202-880A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991865 | ||||||
| chr6:78991960
|
G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2202-975C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991960 | ||||||
| chr6:78992035
|
C | A | 2 | a0002c0002t0028g0260a0002c0002t0028g0261 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2202-1050G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992035 | ||||||
| chr6:78992054
|
C | T | 1 | a0004c0004t0006g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2202-1069G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992054 | ||||||
| chr6:78992058
|
G | T | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2202-1073C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992058 | ||||||
| chr6:78992136
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2202-1151C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992136 | ||||||
| chr6:78992183
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2202-1198G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992183 | ||||||
| chr6:78992184
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2202-1199C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992184 | ||||||
| chr6:78992203
|
C | T | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2202-1218G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992203 | ||||||
| chr6:78992207
|
C | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2202-1222G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992207 | ||||||
| chr6:78992245
|
G | C | 27 | a0002c0002t0004g0022a0002c0002t0004g0198a0002c0002t0004g0207others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.2202-1260C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992245 | ||||||
| chr6:78992255
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2202-1270C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992255 | ||||||
| chr6:78992257
|
C | T | 1 | a0003c0003t0009g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2202-1272G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992257 | ||||||
| chr6:78992482
|
AT | A | 7 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0050others(4): Show | 7 | HG02976.hp1 NA18522.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.2202-1498delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992482 | ||||||
| chr6:78992496
|
C | G | 1 | a0003c0003t0002g0274 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2202-1511G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992496 | ||||||
| chr6:78992583
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-1598C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992583 | ||||||
| chr6:78992631
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-1646A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992631 | ||||||
| chr6:78992813
|
A | T | 2 | a0001c0001t0014g0160a0001c0001t0015g0159 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2202-1828T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992813 | ||||||
| chr6:78992891
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-1906G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992891 | ||||||
| chr6:78992966
|
C | T | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2202-1981G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992966 | ||||||
| chr6:78993018
|
G | A | 36 | a0002c0002t0004g0022a0002c0002t0004g0198a0002c0002t0004g0207others(33): Show | 37 | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.2202-2033C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993018 | ||||||
| chr6:78993079
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2202-2094G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993079 | ||||||
| chr6:78993161
|
T | G | 1 | a0002c0002t0062g0199 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2202-2176A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993161 | ||||||
| chr6:78993180
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2202-2195C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993180 | ||||||
| chr6:78993220
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-2235C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993220 | ||||||
| chr6:78993495
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-2510T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993495 | ||||||
| chr6:78993688
|
A | T | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2202-2703T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993688 | ||||||
| chr6:78993774
|
G | C | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2202-2789C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993774 | ||||||
| chr6:78994011
|
C | T | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2202-3026G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994011 | ||||||
| chr6:78994015
|
A | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0144 | 2 | NA18999.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2202-3030T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994015 | ||||||
| chr6:78994053
|
C | G | 1 | a0002c0009t0004g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2202-3068G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994053 | ||||||
| chr6:78994104
|
G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2202-3119C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994104 | ||||||
| chr6:78994187
|
G | A | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2202-3202C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994187 | ||||||
| chr6:78994230
|
C | T | 10 | a0004c0004t0006g0007a0004c0004t0006g0008a0004c0004t0006g0180others(7): Show | 12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2201+3184G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994230 | ||||||
| chr6:78994305
|
C | T | 1 | a0002c0002t0056g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2201+3109G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994305 | ||||||
| chr6:78994347
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+3067C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994347 | ||||||
| chr6:78994449
|
C | T | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2201+2965G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994449 | ||||||
| chr6:78994450
|
G | A | 1 | a0001c0001t0021g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2201+2964C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994450 | ||||||
| chr6:78994518
|
G | A | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2201+2896C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994518 | ||||||
| chr6:78994577
|
A | AAAAAG | 275 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(272): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.2201+2832_2201+283 others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994577 | ||||||
| chr6:78994615
|
G | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2201+2799C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994615 | ||||||
| chr6:78994746
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+2668T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994746 | ||||||
| chr6:78994983
|
A | G | 1 | a0004c0004t0006g0008 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2201+2431T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994983 | ||||||
| chr6:78995070
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2201+2344C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995070 | ||||||
| chr6:78995183
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+2231G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995183 | ||||||
| chr6:78995212
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0005g0107a0001c0001t0039g0083 | 3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2201+2202A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995212 | ||||||
| chr6:78995267
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+2147T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995267 | ||||||
| chr6:78995418
|
T | C | 6 | a0001c0005t0030g0048a0001c0008t0003g0170a0001c0008t0007g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2201+1996A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995418 | ||||||
| chr6:78995495
|
A | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2201+1919T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995495 | ||||||
| chr6:78995541
|
C | G | 2 | a0002c0002t0004g0208a0002c0002t0008g0209 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2201+1873G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995541 | ||||||
| chr6:78995804
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0141a0001c0001t0005g0140others(1): Show | 5 | HG02257.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2201+1610C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995804 | ||||||
| chr6:78995866
|
G | C | 95 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(92): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.2201+1548C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995866 | ||||||
| chr6:78995890
|
A | G | 4 | a0001c0006t0002g0265a0001c0006t0002g0267a0001c0006t0009g0266others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2201+1524T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995890 | ||||||
| chr6:78996128
|
C | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2201+1286G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996128 | ||||||
| chr6:78996200
|
C | A | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2201+1214G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996200 | ||||||
| chr6:78996257
|
T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2201+1157A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996257 | ||||||
| chr6:78996380
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+1034C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996380 | ||||||
| chr6:78996413
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+1001C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996413 | ||||||
| chr6:78996499
|
C | T | 3 | a0003c0003t0002g0279a0003c0003t0002g0288a0003c0003t0060g0280 | 3 | HG00735.hp1 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2201+915G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996499 | ||||||
| chr6:78996554
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+860C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996554 | ||||||
| chr6:78996579
|
C | T | 1 | a0001c0011t0016g0019 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2201+835G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996579 | ||||||
| chr6:78996713
|
T | C | 2 | a0001c0007t0012g0172a0001c0007t0012g0173 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2201+701A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996713 | ||||||
| chr6:78996821
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+593G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996821 | ||||||
| chr6:78996892
|
C | T | 2 | a0001c0006t0002g0265a0001c0006t0009g0266 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2201+522G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996892 | ||||||
| chr6:78996919
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+495A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996919 | ||||||
| chr6:78996996
|
C | A | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2201+418G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996996 | ||||||
| chr6:78997184
|
A | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2201+230T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997184 | ||||||
| chr6:78997276
|
C | G | 1 | a0001c0001t0001g0124 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2201+138G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997276 | ||||||
| chr6:78997297
|
G | A | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2201+117C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997297 | ||||||
| chr6:78997386
|
G | C | 1 | a0001c0001t0005g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2201+28C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997386 | ||||||
| chr6:78997814
|
T | A | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2018-217A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78997814 | ||||||
| chr6:78997853
|
T | TA | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2018-257dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78997853 | ||||||
| chr6:78997868
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2018-271A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78997868 | ||||||
| chr6:78998023
|
T | C | 4 | a0002c0002t0007g0003a0002c0002t0007g0004a0002c0002t0007g0039others(1): Show | 6 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017+231A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78998023 | ||||||
| chr6:78998147
|
T | C | 1 | a0001c0015t0024g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2017+107A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78998147 | ||||||
| chr6:78998206
|
C | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(93): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.2017+48G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78998206 | ||||||
| chr6:78998435
|
T | G | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1880-44A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998435 | ||||||
| chr6:78998536
|
T | TA | 7 | a0001c0001t0001g0096a0001c0001t0011g0150a0001c0001t0011g0151others(4): Show | 7 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1880-146dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998536 | ||||||
| chr6:78998725
|
A | T | 1 | a0003c0003t0002g0284 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1880-334T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998725 | ||||||
| chr6:78998816
|
T | A | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-425A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998816 | ||||||
| chr6:78998917
|
C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1880-526G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998917 | ||||||
| chr6:78998958
|
ACAATAAC | A | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1880-574_1880-568d others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998958 | ||||||
| chr6:78998974
|
T | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1880-583A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998974 | ||||||
| chr6:78999182
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1880-791C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999182 | ||||||
| chr6:78999220
|
C | T | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1880-829G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999220 | ||||||
| chr6:78999257
|
G | C | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1880-866C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999257 | ||||||
| chr6:78999517
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1880-1126G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999517 | ||||||
| chr6:78999641
|
A | G | 1 | a0002c0009t0004g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1880-1250T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999641 | ||||||
| chr6:78999740
|
G | A | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1880-1349C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999740 | ||||||
| chr6:78999795
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1880-1404A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999795 | ||||||
| chr6:79000249
|
T | G | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1879+1650A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000249 | ||||||
| chr6:79000382
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+1517C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000382 | ||||||
| chr6:79000396
|
T | C | 3 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0044 | 3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1879+1503A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000396 | ||||||
| chr6:79000441
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+1458G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000441 | ||||||
| chr6:79000632
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1879+1267A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000632 | ||||||
| chr6:79000771
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+1128A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000771 | ||||||
| chr6:79000908
|
C | T | 1 | a0001c0007t0012g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1879+991G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000908 | ||||||
| chr6:79000939
|
C | T | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1879+960G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000939 | ||||||
| chr6:79001089
|
C | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(93): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1879+810G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001089 | ||||||
| chr6:79001228
|
C | A | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1879+671G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001228 | ||||||
| chr6:79001461
|
A | G | 6 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0197others(3): Show | 6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1879+438T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001461 | ||||||
| chr6:79001627
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+272A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001627 | ||||||
| chr6:79001724
|
T | A | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1879+175A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001724 | ||||||
| chr6:79002224
|
C | T | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1654-100G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002224 | ||||||
| chr6:79002255
|
A | G | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1654-131T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002255 | ||||||
| chr6:79002284
|
G | C | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1654-160C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002284 | ||||||
| chr6:79002294
|
T | C | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1654-170A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002294 | ||||||
| chr6:79002412
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1654-288A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002412 | ||||||
| chr6:79002481
|
C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1654-357G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002481 | ||||||
| chr6:79002637
|
G | A | 4 | a0001c0006t0002g0265a0001c0006t0002g0267a0001c0006t0009g0266others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-513C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002637 | ||||||
| chr6:79002895
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1654-771C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002895 | ||||||
| chr6:79003222
|
T | C | 2 | a0001c0001t0014g0160a0001c0001t0015g0159 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1653+508A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003222 | ||||||
| chr6:79003321
|
A | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0133others(4): Show | 7 | HG02145.hp2 NA18960.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1653+409T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003321 | ||||||
| chr6:79003331
|
G | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1653+399C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003331 | ||||||
| chr6:79003429
|
C | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1653+301G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003429 | ||||||
| chr6:79003448
|
T | C | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1653+282A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003448 | ||||||
| chr6:79003485
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1653+245C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003485 | ||||||
| chr6:79003536
|
C | T | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1653+194G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003536 | ||||||
| chr6:79003569
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1653+161G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003569 | ||||||
| chr6:79003673
|
C | A | 2 | a0003c0003t0002g0286a0003c0003t0031g0273 | 2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1653+57G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003673 | ||||||
| chr6:79003895
|
T | G | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-37A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79003895 | ||||||
| chr6:79004224
|
C | T | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1525-366G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004224 | ||||||
| chr6:79004228
|
T | G | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1525-370A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004228 | ||||||
| chr6:79004313
|
G | A | 1 | a0001c0001t0050g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1525-455C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004313 | ||||||
| chr6:79004350
|
G | A | 2 | a0002c0002t0004g0219a0002c0002t0010g0218 | 2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1525-492C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004350 | ||||||
| chr6:79004991
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(141): Show | 148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1525-1133G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004991 | ||||||
| chr6:79005070
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-1212A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005070 | ||||||
| chr6:79005150
|
T | C | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1525-1292A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005150 | ||||||
| chr6:79005213
|
T | C | 5 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0050others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-1355A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005213 | ||||||
| chr6:79005236
|
T | C | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1525-1378A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005236 | ||||||
| chr6:79005252
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-1394A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005252 | ||||||
| chr6:79005308
|
A | G | 1 | a0001c0001t0040g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1525-1450T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005308 | ||||||
| chr6:79005776
|
T | C | 8 | a0001c0001t0014g0158a0001c0001t0014g0160a0001c0001t0014g0161others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-1918A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005776 | ||||||
| chr6:79005881
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1525-2023G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005881 | ||||||
| chr6:79005903
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(141): Show | 148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1525-2045C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005903 | ||||||
| chr6:79006050
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1525-2192A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006050 | ||||||
| chr6:79006380
|
C | CTGGTTTT others(8): Show |
3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-2537_1525-252 others(19): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006380 | ||||||
| chr6:79006396
|
T | C | 5 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0050others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-2538A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006396 | ||||||
| chr6:79006407
|
A | G | 1 | a0001c0001t0018g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1525-2549T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006407 | ||||||
| chr6:79006493
|
A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1525-2635T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006493 | ||||||
| chr6:79006523
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-2665A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006523 | ||||||
| chr6:79006623
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-2765C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006623 | ||||||
| chr6:79006945
|
A | AAAAG | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3088_1525-308 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006945 | ||||||
| chr6:79007000
|
G | A | 6 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-3142C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007000 | ||||||
| chr6:79007047
|
T | A | 4 | a0001c0001t0011g0029a0001c0001t0021g0027a0001c0001t0021g0028others(1): Show | 4 | HG02922.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-3189A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007047 | ||||||
| chr6:79007603
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3745A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007603 | ||||||
| chr6:79007609
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1525-3751A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007609 | ||||||
| chr6:79007613
|
G | C | 1 | a0001c0001t0069g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1525-3755C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007613 | ||||||
| chr6:79007654
|
C | CT | 11 | a0001c0006t0002g0013a0001c0006t0002g0268a0001c0008t0003g0170others(8): Show | 12 | HG01358.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1525-3797dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | ||||||
| chr6:79007654
|
CT | C | 27 | a0001c0001t0011g0029a0001c0001t0011g0255a0001c0001t0014g0158others(24): Show | 27 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1525-3797delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | ||||||
| chr6:79007654
|
CTT | C | 8 | a0001c0001t0011g0256a0001c0001t0017g0023a0001c0001t0017g0026others(5): Show | 8 | HG00642.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-3798_1525-379 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | ||||||
| chr6:79007654
|
CTTT | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(89): Show | 93 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1525-3799_1525-379 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | ||||||
| chr6:79007686
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3828C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007686 | ||||||
| chr6:79007698
|
A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1525-3840T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007698 | ||||||
| chr6:79007766
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3908A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007766 | ||||||
| chr6:79007783
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3925G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007783 | ||||||
| chr6:79007807
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3949C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007807 | ||||||
| chr6:79007870
|
CT | C | 3 | a0001c0001t0021g0027a0001c0001t0021g0028a0001c0001t0021g0030 | 3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1525-4013delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007870 | ||||||
| chr6:79007883
|
G | A | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1525-4025C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007883 | ||||||
| chr6:79007941
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1525-4083A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007941 | ||||||
| chr6:79008021
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0141a0001c0001t0005g0140others(2): Show | 6 | HG01358.hp1 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-4163G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008021 | ||||||
| chr6:79008026
|
G | A | 2 | a0001c0001t0026g0149a0001c0001t0026g0154 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1525-4168C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008026 | ||||||
| chr6:79008066
|
A | AG | 283 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(280): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1525-4209_1525-420 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008066 | ||||||
| chr6:79008088
|
G | A | 1 | a0001c0001t0011g0256 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1525-4230C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008088 | ||||||
| chr6:79008199
|
A | T | 1 | a0001c0007t0012g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1525-4341T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008199 | ||||||
| chr6:79008205
|
C | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-4347G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008205 | ||||||
| chr6:79008355
|
T | C | 4 | a0002c0002t0003g0201a0002c0002t0003g0202a0002c0002t0003g0203others(1): Show | 4 | NA18945.hp2 NA18974.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-4497A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008355 | ||||||
| chr6:79008374
|
T | C | 1 | a0001c0001t0014g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1525-4516A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008374 | ||||||
| chr6:79008584
|
CT | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1525-4727delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008584 | ||||||
| chr6:79008780
|
C | T | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1525-4922G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008780 | ||||||
| chr6:79008797
|
C | T | 15 | a0002c0002t0003g0201a0002c0002t0003g0202a0002c0002t0003g0203others(12): Show | 15 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1525-4939G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008797 | ||||||
| chr6:79009013
|
TCCTA | T | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1525-5159_1525-515 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009013 | ||||||
| chr6:79009078
|
T | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1525-5220A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009078 | ||||||
| chr6:79009121
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1525-5263G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009121 | ||||||
| chr6:79009132
|
G | A | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1525-5274C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009132 | ||||||
| chr6:79009411
|
C | G | 3 | a0001c0006t0002g0013a0001c0006t0002g0268a0001c0006t0002g0275 | 4 | NA19011.hp1 NA19057.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-5553G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009411 | ||||||
| chr6:79009496
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1524+5586A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009496 | ||||||
| chr6:79009739
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+5343C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009739 | ||||||
| chr6:79009818
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+5264G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009818 | ||||||
| chr6:79009877
|
A | T | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+5205T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009877 | ||||||
| chr6:79009878
|
G | A | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+5204C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009878 | ||||||
| chr6:79009906
|
C | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1524+5176G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009906 | ||||||
| chr6:79009908
|
T | TGAAA | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1524+5170_1524+517 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009908 | ||||||
| chr6:79010042
|
T | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1524+5040A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010042 | ||||||
| chr6:79010052
|
TAGGAAGA others(4): Show |
T | 5 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0050others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+5019_1524+502 others(15): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010052 | ||||||
| chr6:79010220
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+4862A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010220 | ||||||
| chr6:79010403
|
T | A | 37 | a0001c0005t0054g0038a0001c0006t0002g0013a0001c0006t0002g0014others(34): Show | 43 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1524+4679A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010403 | ||||||
| chr6:79010505
|
C | CA | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1524+4576dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010505 | ||||||
| chr6:79010862
|
G | A | 5 | a0001c0001t0005g0095a0001c0006t0002g0265a0001c0006t0002g0267others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+4220C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010862 | ||||||
| chr6:79011023
|
AG | A | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1524+4058delC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011023 | ||||||
| chr6:79011090
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+3992C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011090 | ||||||
| chr6:79011150
|
T | A | 127 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1524+3932A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011150 | ||||||
| chr6:79011150
|
T | G | 1 | a0001c0001t0014g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1524+3932A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011150 | ||||||
| chr6:79011151
|
G | A | 2 | a0002c0002t0004g0216a0002c0002t0004g0217 | 2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1524+3931C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011151 | ||||||
| chr6:79011152
|
T | G | 2 | a0001c0001t0014g0158a0001c0001t0015g0155 | 2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1524+3930A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011152 | ||||||
| chr6:79011322
|
AGTTT | A | 3 | a0001c0001t0001g0082a0001c0001t0005g0107a0001c0001t0039g0083 | 3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1524+3756_1524+375 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011322 | ||||||
| chr6:79011445
|
C | T | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+3637G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011445 | ||||||
| chr6:79011505
|
G | A | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+3577C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011505 | ||||||
| chr6:79011623
|
C | G | 1 | a0002c0002t0008g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1524+3459G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011623 | ||||||
| chr6:79011692
|
C | A | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1524+3390G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011692 | ||||||
| chr6:79011905
|
AG | A | 4 | a0001c0006t0002g0265a0001c0006t0002g0267a0001c0006t0009g0266others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+3176delC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011905 | ||||||
| chr6:79012183
|
T | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1524+2899A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012183 | ||||||
| chr6:79012236
|
G | T | 8 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0003others(5): Show | 10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2846C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012236 | ||||||
| chr6:79012266
|
G | C | 1 | a0002c0002t0004g0215 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1524+2816C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012266 | ||||||
| chr6:79012307
|
T | C | 1 | a0002c0002t0003g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1524+2775A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012307 | ||||||
| chr6:79012318
|
T | C | 1 | a0002c0002t0004g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1524+2764A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012318 | ||||||
| chr6:79012329
|
C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1524+2753G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012329 | ||||||
| chr6:79012354
|
T | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+2728A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012354 | ||||||
| chr6:79012922
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1524+2160T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012922 | ||||||
| chr6:79012955
|
A | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1524+2127T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012955 | ||||||
| chr6:79013112
|
CA | C | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+1969delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013112 | ||||||
| chr6:79013135
|
T | C | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1524+1947A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013135 | ||||||
| chr6:79013298
|
G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1524+1784C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013298 | ||||||
| chr6:79013372
|
C | A | 1 | a0004c0004t0006g0008 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1524+1710G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013372 | ||||||
| chr6:79013437
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1524+1645T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013437 | ||||||
| chr6:79013719
|
C | T | 1 | a0001c0001t0011g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1524+1363G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013719 | ||||||
| chr6:79013934
|
C | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(141): Show | 148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1524+1148G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013934 | ||||||
| chr6:79014038
|
T | A | 98 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(95): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1524+1044A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014038 | ||||||
| chr6:79014039
|
T | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(95): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1524+1043A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014039 | ||||||
| chr6:79014058
|
T | C | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1524+1024A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014058 | ||||||
| chr6:79014067
|
T | TTACAAAC others(208): Show |
4 | a0001c0006t0002g0013a0001c0006t0002g0268a0001c0006t0002g0271others(1): Show | 5 | HG01123.hp1 NA19011.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(219): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | ||||||
| chr6:79014067
|
T | TTACAAAC others(216): Show |
1 | a0001c0006t0002g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1524+1014_1524+101 others(227): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | ||||||
| chr6:79014067
|
T | TTACAAAC others(217): Show |
29 | a0001c0006t0002g0014a0001c0006t0002g0267a0001c0006t0002g0269others(26): Show | 33 | HG00099.hp2 HG01070.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(228): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | ||||||
| chr6:79014067
|
T | TTACAAAC others(217): Show |
3 | a0003c0003t0002g0279a0003c0003t0002g0288a0003c0003t0060g0280 | 3 | HG00735.hp1 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(228): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | ||||||
| chr6:79014067
|
T | TTACAAAC others(218): Show |
2 | a0003c0003t0002g0032a0003c0003t0009g0016 | 3 | NA18955.hp1 NA19002.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(229): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | ||||||
| chr6:79014067
|
T | TTACAAAC others(219): Show |
1 | a0003c0003t0052g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1524+1014_1524+101 others(230): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | ||||||
| chr6:79014171
|
G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1524+911C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014171 | ||||||
| chr6:79014354
|
A | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1524+728T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014354 | ||||||
| chr6:79014489
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0108a0001c0001t0069g0117 | 3 | NA18950.hp1 NA19012.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1524+593A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014489 | ||||||
| chr6:79014569
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+513T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014569 | ||||||
| chr6:79014662
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+420C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014662 | ||||||
| chr6:79014707
|
C | CCAT | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+374_1524+375i others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014707 | ||||||
| chr6:79014709
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+373T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014709 | ||||||
| chr6:79014712
|
G | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1524+370C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014712 | ||||||
| chr6:79014983
|
A | C | 1 | a0001c0001t0043g0104 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1524+99T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014983 | ||||||
| chr6:79015023
|
C | A | 36 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0268others(33): Show | 42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1524+59G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79015023 | ||||||
| chr6:79015395
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1390-179G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 14/39 | chr6 | 79015395 | ||||||
| chr6:79015905
|
G | A | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1236-122C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79015905 | ||||||
| chr6:79015943
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0005g0140 | 3 | HG02257.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1236-160G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79015943 | ||||||
| chr6:79016008
|
T | A | 5 | a0002c0002t0004g0022a0002c0002t0004g0221a0002c0002t0004g0229others(2): Show | 5 | HG02523.hp2 NA18612.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236-225A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016008 | ||||||
| chr6:79016018
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1236-235T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016018 | ||||||
| chr6:79016423
|
T | C | 1 | a0001c0001t0005g0107 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1235+121A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016423 | ||||||
| chr6:79016535
|
A | T | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235+9T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016535 | ||||||
| chr6:79016722
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0108a0001c0001t0005g0076others(2): Show | 5 | NA18950.hp1 NA18975.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-80A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79016722 | ||||||
| chr6:79016791
|
A | C | 4 | a0002c0002t0004g0022a0002c0002t0004g0221a0002c0002t0004g0229others(1): Show | 4 | HG02523.hp2 NA18612.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-149T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79016791 | ||||||
| chr6:79016889
|
C | T | 4 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(1): Show | 4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-247G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79016889 | ||||||
| chr6:79017033
|
T | A | 72 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0193others(69): Show | 75 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1136+313A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79017033 | ||||||
| chr6:79017306
|
A | C | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1136+40T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79017306 | ||||||
| chr6:79017422
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1096-36C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 11/39 | chr6 | 79017422 | ||||||
| chr6:79017621
|
T | C | 1 | a0002c0002t0028g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.995-38A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017621 | ||||||
| chr6:79017661
|
C | T | 2 | a0001c0001t0005g0064a0001c0001t0014g0158 | 2 | HG04115.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.995-78G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017661 | ||||||
| chr6:79017671
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.995-88C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017671 | ||||||
| chr6:79017739
|
T | G | 1 | a0002c0002t0004g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.995-156A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017739 | ||||||
| chr6:79017770
|
C | CTT | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.995-188_995-187ins others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017770 | ||||||
| chr6:79017976
|
A | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.995-393T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017976 | ||||||
| chr6:79018180
|
C | A | 1 | a0003c0003t0002g0274 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.995-597G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018180 | ||||||
| chr6:79018361
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.994+728C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018361 | ||||||
| chr6:79018431
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0005g0299 | 2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.994+658G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018431 | ||||||
| chr6:79018495
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.994+594G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018495 | ||||||
| chr6:79018588
|
T | C | 2 | a0001c0005t0049g0036a0001c0005t0054g0038 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.994+501A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018588 | ||||||
| chr6:79018611
|
T | G | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.994+478A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018611 | ||||||
| chr6:79018671
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.994+418G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018671 | ||||||
| chr6:79018721
|
ACTATAGA others(4): Show |
A | 1 | a0003c0003t0002g0289 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.994+357_994+367del others(11): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018721 | ||||||
| chr6:79018778
|
T | C | 1 | a0003c0003t0009g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.994+311A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018778 | ||||||
| chr6:79018867
|
T | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.994+222A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018867 | ||||||
| chr6:79019016
|
A | T | 2 | a0001c0011t0016g0017a0001c0011t0016g0018 | 2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.994+73T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79019016 | ||||||
| chr6:79019189
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.924-30A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019189 | ||||||
| chr6:79019286
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.924-127T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019286 | ||||||
| chr6:79019321
|
G | T | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.924-162C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019321 | ||||||
| chr6:79019381
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-222T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019381 | ||||||
| chr6:79019665
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-506T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019665 | ||||||
| chr6:79019736
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-577G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019736 | ||||||
| chr6:79019772
|
A | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.924-613T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019772 | ||||||
| chr6:79019772
|
A | G | 1 | a0004c0004t0006g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.924-613T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019772 | ||||||
| chr6:79019856
|
T | C | 1 | a0003c0003t0031g0273 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.924-697A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019856 | ||||||
| chr6:79019867
|
C | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-708G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019867 | ||||||
| chr6:79019931
|
A | G | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.924-772T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019931 | ||||||
| chr6:79019947
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-788C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019947 | ||||||
| chr6:79020170
|
T | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0060others(132): Show | 142 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.924-1011A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020170 | ||||||
| chr6:79020171
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-1012T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020171 | ||||||
| chr6:79020286
|
A | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.924-1127T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020286 | ||||||
| chr6:79020333
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.924-1174A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020333 | ||||||
| chr6:79020495
|
A | G | 1 | a0001c0006t0002g0268 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.924-1336T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020495 | ||||||
| chr6:79020573
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-1414T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020573 | ||||||
| chr6:79021286
|
A | G | 1 | a0001c0001t0005g0098 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.924-2127T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021286 | ||||||
| chr6:79021356
|
C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924-2197G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021356 | ||||||
| chr6:79021482
|
C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924-2323G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021482 | ||||||
| chr6:79021524
|
C | A | 1 | a0001c0001t0011g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.924-2365G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021524 | ||||||
| chr6:79022045
|
A | C | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.924-2886T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022045 | ||||||
| chr6:79022085
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-2926C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022085 | ||||||
| chr6:79022123
|
G | A | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.924-2964C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022123 | ||||||
| chr6:79022170
|
G | A | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.924-3011C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022170 | ||||||
| chr6:79022269
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-3110C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022269 | ||||||
| chr6:79022332
|
T | C | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.924-3173A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022332 | ||||||
| chr6:79022365
|
A | G | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.923+3154T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022365 | ||||||
| chr6:79022473
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+3046G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022473 | ||||||
| chr6:79022484
|
C | T | 5 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0197others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+3035G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022484 | ||||||
| chr6:79022534
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+2985C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022534 | ||||||
| chr6:79022881
|
G | C | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.923+2638C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022881 | ||||||
| chr6:79022965
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+2554A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022965 | ||||||
| chr6:79023123
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+2396C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023123 | ||||||
| chr6:79023459
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.923+2060T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023459 | ||||||
| chr6:79023631
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.923+1888A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023631 | ||||||
| chr6:79023701
|
T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.923+1818A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023701 | ||||||
| chr6:79023965
|
C | G | 2 | a0001c0005t0038g0047a0001c0005t0045g0046 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.923+1554G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023965 | ||||||
| chr6:79024049
|
C | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1470G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024049 | ||||||
| chr6:79024050
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+1469C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024050 | ||||||
| chr6:79024247
|
C | T | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+1272G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024247 | ||||||
| chr6:79024326
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+1193G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024326 | ||||||
| chr6:79024514
|
T | C | 1 | a0002c0002t0010g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.923+1005A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024514 | ||||||
| chr6:79024527
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.923+992C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024527 | ||||||
| chr6:79024530
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+989G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024530 | ||||||
| chr6:79024532
|
C | T | 91 | a0001c0005t0038g0047a0001c0005t0045g0046a0001c0008t0003g0170others(88): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.923+987G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024532 | ||||||
| chr6:79024579
|
C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.923+940G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024579 | ||||||
| chr6:79024652
|
A | C | 130 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(127): Show | 131 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.923+867T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024652 | ||||||
| chr6:79024661
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.923+858G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024661 | ||||||
| chr6:79024667
|
T | C | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+852A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024667 | ||||||
| chr6:79024713
|
G | A | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.923+806C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024713 | ||||||
| chr6:79024760
|
G | A | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.923+759C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024760 | ||||||
| chr6:79024806
|
A | AAAAT | 11 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(8): Show | 11 | HG01496.hp2 HG02055.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+709_923+712dup others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024806 | ||||||
| chr6:79024836
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+683T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024836 | ||||||
| chr6:79025009
|
C | T | 132 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(129): Show | 133 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.923+510G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025009 | ||||||
| chr6:79025226
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.923+293A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025226 | ||||||
| chr6:79025281
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+238C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025281 | ||||||
| chr6:79025306
|
G | GA | 253 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0060others(250): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.923+212dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025306 | ||||||
| chr6:79025437
|
C | T | 5 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(2): Show | 5 | HG02258.hp2 HG02602.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+82G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025437 | ||||||
| chr6:79025460
|
T | C | 1 | a0003c0003t0002g0294 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.923+59A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025460 | ||||||
| chr6:79025899
|
T | TAACAACA others(5): Show |
3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.822+32_822+43dupGT others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 8/39 | chr6 | 79025899 | ||||||
| chr6:79026239
|
C | T | 1 | a0002c0002t0004g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.601-75G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026239 | ||||||
| chr6:79026369
|
C | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.601-205G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026369 | ||||||
| chr6:79026397
|
C | T | 1 | a0003c0003t0002g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601-233G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026397 | ||||||
| chr6:79026467
|
TA | T | 283 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(280): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.601-304delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026467 | ||||||
| chr6:79026722
|
G | GT | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-559dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026722 | ||||||
| chr6:79026889
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-725T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026889 | ||||||
| chr6:79026892
|
G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-728C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026892 | ||||||
| chr6:79027121
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-957A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027121 | ||||||
| chr6:79027169
|
A | G | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.601-1005T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027169 | ||||||
| chr6:79027306
|
C | T | 2 | a0002c0002t0010g0206a0002c0002t0010g0234 | 2 | HG02080.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.601-1142G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027306 | ||||||
| chr6:79027389
|
A | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.601-1225T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027389 | ||||||
| chr6:79027394
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.601-1230A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027394 | ||||||
| chr6:79027466
|
G | A | 1 | a0003c0003t0002g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601-1302C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027466 | ||||||
| chr6:79027812
|
T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-1648A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027812 | ||||||
| chr6:79027834
|
C | G | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-1670G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027834 | ||||||
| chr6:79027905
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-1741C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027905 | ||||||
| chr6:79027915
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-1751C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027915 | ||||||
| chr6:79028089
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0146a0001c0001t0005g0145 | 3 | NA18612.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.601-1925T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028089 | ||||||
| chr6:79028307
|
C | G | 1 | a0001c0001t0050g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.601-2143G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028307 | ||||||
| chr6:79028330
|
TA | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-2167delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028330 | ||||||
| chr6:79028632
|
T | C | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601-2468A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028632 | ||||||
| chr6:79028873
|
T | C | 2 | a0004c0004t0013g0182a0004c0004t0065g0183 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.601-2709A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028873 | ||||||
| chr6:79029174
|
T | A | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-3010A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029174 | ||||||
| chr6:79029242
|
C | T | 2 | a0002c0002t0007g0004a0002c0002t0007g0040 | 3 | HG00099.hp1 HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.601-3078G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029242 | ||||||
| chr6:79029255
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-3091A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029255 | ||||||
| chr6:79029272
|
G | A | 5 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(2): Show | 5 | HG01358.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-3108C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029272 | ||||||
| chr6:79029291
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.601-3127G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029291 | ||||||
| chr6:79029293
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.601-3129C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029293 | ||||||
| chr6:79029350
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-3186T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029350 | ||||||
| chr6:79029388
|
G | A | 297 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(294): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.601-3224C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029388 | ||||||
| chr6:79029415
|
CTATACAA | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-3258_601-3252d others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029415 | ||||||
| chr6:79029576
|
C | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-3412G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029576 | ||||||
| chr6:79029633
|
G | A | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.601-3469C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029633 | ||||||
| chr6:79029688
|
C | T | 1 | a0001c0015t0024g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-3524G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029688 | ||||||
| chr6:79029793
|
G | T | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-3629C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029793 | ||||||
| chr6:79029872
|
A | T | 3 | a0003c0003t0002g0279a0003c0003t0002g0288a0003c0003t0060g0280 | 3 | HG00735.hp1 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.601-3708T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029872 | ||||||
| chr6:79029905
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(132): Show | 136 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.601-3741C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029905 | ||||||
| chr6:79030050
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-3886C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030050 | ||||||
| chr6:79030083
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0105 | 3 | NA18941.hp1 NA19056.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.601-3919A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030083 | ||||||
| chr6:79030196
|
G | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4032C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030196 | ||||||
| chr6:79030377
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4213A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030377 | ||||||
| chr6:79030441
|
AAAGT | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4281_601-4278d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030441 | ||||||
| chr6:79030556
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4392G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030556 | ||||||
| chr6:79030685
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4521A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030685 | ||||||
| chr6:79030698
|
G | A | 1 | a0001c0006t0002g0014 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601-4534C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030698 | ||||||
| chr6:79030715
|
T | C | 1 | a0002c0002t0003g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.601-4551A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030715 | ||||||
| chr6:79030729
|
A | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0108a0001c0001t0069g0117 | 3 | NA18950.hp1 NA19012.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.601-4565T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030729 | ||||||
| chr6:79030817
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4653A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030817 | ||||||
| chr6:79030849
|
C | T | 1 | a0001c0011t0016g0018 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.601-4685G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030849 | ||||||
| chr6:79030887
|
AAAGAT | A | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.601-4728_601-4724d others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030887 | ||||||
| chr6:79030931
|
G | GT | 4 | a0001c0005t0003g0001a0001c0006t0008g0037a0001c0011t0016g0018others(1): Show | 6 | HG02280.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-4768dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030931 | ||||||
| chr6:79030937
|
T | G | 2 | a0001c0001t0001g0138a0001c0001t0005g0065 | 2 | HG02451.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.601-4773A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030937 | ||||||
| chr6:79030940
|
T | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-4776A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030940 | ||||||
| chr6:79030941
|
G | T | 5 | a0001c0006t0002g0013a0001c0006t0002g0268a0001c0011t0016g0017others(2): Show | 6 | NA19003.hp1 NA19011.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-4777C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030941 | ||||||
| chr6:79031004
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-4840A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031004 | ||||||
| chr6:79031060
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.601-4896G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031060 | ||||||
| chr6:79031100
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4936G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031100 | ||||||
| chr6:79031203
|
T | C | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.601-5039A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031203 | ||||||
| chr6:79031219
|
T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-5055A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031219 | ||||||
| chr6:79031304
|
C | T | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-5140G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031304 | ||||||
| chr6:79031502
|
T | C | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-5338A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031502 | ||||||
| chr6:79032055
|
G | A | 1 | a0004c0004t0013g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601-5891C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032055 | ||||||
| chr6:79032105
|
A | T | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-5941T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032105 | ||||||
| chr6:79032109
|
A | G | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-5945T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032109 | ||||||
| chr6:79032137
|
T | C | 1 | a0004c0004t0006g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.601-5973A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032137 | ||||||
| chr6:79032156
|
T | G | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.601-5992A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032156 | ||||||
| chr6:79032197
|
AG | A | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6034delC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032197 | ||||||
| chr6:79032241
|
A | G | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.601-6077T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032241 | ||||||
| chr6:79032384
|
C | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.601-6220G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032384 | ||||||
| chr6:79032509
|
T | C | 1 | a0003c0003t0002g0294 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601-6345A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032509 | ||||||
| chr6:79032634
|
T | C | 10 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(7): Show | 13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6470A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032634 | ||||||
| chr6:79032661
|
G | A | 4 | a0001c0001t0011g0029a0001c0001t0021g0027a0001c0001t0021g0028others(1): Show | 4 | HG02922.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6497C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032661 | ||||||
| chr6:79033096
|
G | A | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-6932C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033096 | ||||||
| chr6:79033120
|
C | T | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.601-6956G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033120 | ||||||
| chr6:79033230
|
G | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(93): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.601-7066C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033230 | ||||||
| chr6:79033315
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0005g0107a0001c0001t0039g0083 | 3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.601-7151A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033315 | ||||||
| chr6:79033339
|
T | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0102others(1): Show | 4 | HG02074.hp2 HG02155.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-7175A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033339 | ||||||
| chr6:79033375
|
C | G | 1 | a0002c0002t0010g0228 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.601-7211G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033375 | ||||||
| chr6:79033402
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-7238C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033402 | ||||||
| chr6:79033485
|
T | C | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.601-7321A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033485 | ||||||
| chr6:79033494
|
T | C | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601-7330A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033494 | ||||||
| chr6:79033601
|
T | G | 3 | a0004c0004t0013g0182a0004c0004t0013g0184a0004c0004t0065g0183 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601-7437A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033601 | ||||||
| chr6:79033803
|
A | G | 5 | a0002c0002t0003g0201a0002c0002t0003g0202a0002c0002t0003g0203others(2): Show | 5 | NA18945.hp2 NA18974.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-7639T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033803 | ||||||
| chr6:79034006
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-7842T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034006 | ||||||
| chr6:79034018
|
G | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(139): Show | 146 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.601-7854C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034018 | ||||||
| chr6:79034063
|
T | C | 1 | a0002c0002t0003g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.601-7899A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034063 | ||||||
| chr6:79034160
|
G | A | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601-7996C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034160 | ||||||
| chr6:79034327
|
T | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-8163A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034327 | ||||||
| chr6:79034363
|
C | T | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.601-8199G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034363 | ||||||
| chr6:79034865
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+7978G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034865 | ||||||
| chr6:79035128
|
T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.600+7715A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035128 | ||||||
| chr6:79035151
|
C | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(93): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.600+7692G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035151 | ||||||
| chr6:79035270
|
T | C | 1 | a0001c0011t0016g0019 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.600+7573A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035270 | ||||||
| chr6:79035332
|
C | A | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600+7511G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035332 | ||||||
| chr6:79035390
|
C | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(132): Show | 136 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.600+7453G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035390 | ||||||
| chr6:79035402
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+7441G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035402 | ||||||
| chr6:79035410
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.600+7433A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035410 | ||||||
| chr6:79035432
|
A | G | 4 | a0003c0003t0002g0002a0003c0003t0002g0278a0003c0003t0009g0277others(1): Show | 6 | NA18950.hp2 NA18960.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+7411T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035432 | ||||||
| chr6:79035504
|
A | G | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+7339T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035504 | ||||||
| chr6:79035560
|
C | G | 36 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0268others(33): Show | 42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.600+7283G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035560 | ||||||
| chr6:79035758
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.600+7085T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035758 | ||||||
| chr6:79035788
|
G | A | 6 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0197others(3): Show | 6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+7055C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035788 | ||||||
| chr6:79035820
|
G | A | 1 | a0003c0003t0052g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.600+7023C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035820 | ||||||
| chr6:79035839
|
T | C | 35 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(32): Show | 35 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.600+7004A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035839 | ||||||
| chr6:79035855
|
C | G | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.600+6988G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035855 | ||||||
| chr6:79035870
|
C | T | 1 | a0002c0002t0068g0220 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.600+6973G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035870 | ||||||
| chr6:79035964
|
C | T | 10 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(7): Show | 13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+6879G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035964 | ||||||
| chr6:79036034
|
A | G | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.600+6809T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036034 | ||||||
| chr6:79036195
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+6648G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036195 | ||||||
| chr6:79036331
|
T | A | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.600+6512A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036331 | ||||||
| chr6:79036349
|
T | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+6494A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036349 | ||||||
| chr6:79036405
|
ACT | A | 9 | a0001c0001t0014g0158a0001c0001t0014g0160a0001c0001t0014g0161others(6): Show | 9 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+6436_600+6437d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036405 | ||||||
| chr6:79036435
|
T | C | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.600+6408A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036435 | ||||||
| chr6:79036437
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+6406G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036437 | ||||||
| chr6:79036636
|
C | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+6207G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036636 | ||||||
| chr6:79036688
|
G | A | 1 | a0001c0001t0005g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.600+6155C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036688 | ||||||
| chr6:79036756
|
C | A | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.600+6087G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036756 | ||||||
| chr6:79036757
|
T | A | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.600+6086A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036757 | ||||||
| chr6:79036921
|
C | CA | 112 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(109): Show | 115 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.600+5921dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | ||||||
| chr6:79036921
|
C | CAA | 26 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0001g0097others(23): Show | 26 | HG00621.hp2 HG00738.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.600+5920_600+5921d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | ||||||
| chr6:79036921
|
CA | C | 9 | a0001c0005t0038g0047a0001c0007t0012g0172a0001c0007t0012g0173others(6): Show | 9 | HG01070.hp1 HG01358.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.600+5921delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | ||||||
| chr6:79036921
|
CAA | C | 7 | a0001c0001t0026g0149a0001c0005t0023g0049a0001c0005t0023g0051others(4): Show | 7 | HG01884.hp2 HG02886.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+5920_600+5921d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | ||||||
| chr6:79037076
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.600+5767T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037076 | ||||||
| chr6:79037103
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.600+5740A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037103 | ||||||
| chr6:79037174
|
C | T | 291 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(288): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.600+5669G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037174 | ||||||
| chr6:79037267
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.600+5576T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037267 | ||||||
| chr6:79037321
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+5522G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037321 | ||||||
| chr6:79037378
|
C | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600+5465G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037378 | ||||||
| chr6:79037506
|
G | A | 1 | a0002c0002t0003g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.600+5337C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037506 | ||||||
| chr6:79037727
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.600+5116T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037727 | ||||||
| chr6:79037879
|
A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.600+4964T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037879 | ||||||
| chr6:79037880
|
T | C | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+4963A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037880 | ||||||
| chr6:79037880
|
T | TAAC | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+4960_600+4962d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037880 | ||||||
| chr6:79037915
|
T | C | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.600+4928A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037915 | ||||||
| chr6:79037965
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.600+4878A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037965 | ||||||
| chr6:79037978
|
T | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600+4865A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037978 | ||||||
| chr6:79038011
|
C | T | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+4832G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038011 | ||||||
| chr6:79038117
|
T | C | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+4726A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038117 | ||||||
| chr6:79038288
|
T | G | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+4555A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038288 | ||||||
| chr6:79038336
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.600+4507G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038336 | ||||||
| chr6:79038392
|
C | T | 2 | a0002c0002t0004g0219a0002c0002t0010g0218 | 2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.600+4451G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038392 | ||||||
| chr6:79038464
|
G | C | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+4379C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038464 | ||||||
| chr6:79038611
|
C | T | 283 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(280): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.600+4232G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038611 | ||||||
| chr6:79038666
|
CTTT | C | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.600+4174_600+4176d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038666 | ||||||
| chr6:79038704
|
A | G | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+4139T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038704 | ||||||
| chr6:79038724
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+4119A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038724 | ||||||
| chr6:79039005
|
C | A | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+3838G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039005 | ||||||
| chr6:79039160
|
CCACAT | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+3678_600+3682d others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039160 | ||||||
| chr6:79039254
|
G | A | 1 | a0001c0006t0009g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.600+3589C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039254 | ||||||
| chr6:79039415
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.600+3428A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039415 | ||||||
| chr6:79039449
|
CTT | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(142): Show | 149 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.600+3392_600+3393d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039449 | ||||||
| chr6:79039460
|
AT | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+3382delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039460 | ||||||
| chr6:79039515
|
T | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+3328A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039515 | ||||||
| chr6:79039732
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+3111A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039732 | ||||||
| chr6:79039877
|
T | C | 95 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(92): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.600+2966A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039877 | ||||||
| chr6:79039940
|
C | G | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.600+2903G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039940 | ||||||
| chr6:79039947
|
A | G | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2896T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039947 | ||||||
| chr6:79040003
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+2840G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040003 | ||||||
| chr6:79040092
|
T | C | 284 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(281): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.600+2751A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040092 | ||||||
| chr6:79040179
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0005g0145 | 2 | NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.600+2664A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040179 | ||||||
| chr6:79040476
|
A | T | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.600+2367T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040476 | ||||||
| chr6:79040668
|
T | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(132): Show | 136 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.600+2175A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040668 | ||||||
| chr6:79040863
|
C | A | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.600+1980G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040863 | ||||||
| chr6:79040896
|
C | CT | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.600+1946dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040896 | ||||||
| chr6:79041031
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.600+1812T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041031 | ||||||
| chr6:79041058
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+1785A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041058 | ||||||
| chr6:79041300
|
T | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+1543A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041300 | ||||||
| chr6:79041477
|
C | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.600+1366G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041477 | ||||||
| chr6:79041724
|
A | C | 8 | a0002c0002t0003g0237a0002c0002t0003g0238a0002c0002t0003g0249others(5): Show | 8 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.600+1119T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041724 | ||||||
| chr6:79041761
|
C | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.600+1082G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041761 | ||||||
| chr6:79041764
|
A | T | 1 | a0002c0002t0003g0244 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.600+1079T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041764 | ||||||
| chr6:79042273
|
T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600+570A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042273 | ||||||
| chr6:79042346
|
A | C | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.600+497T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042346 | ||||||
| chr6:79042490
|
C | A | 1 | a0002c0002t0003g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.600+353G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042490 | ||||||
| chr6:79042587
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+256C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042587 | ||||||
| chr6:79042623
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+220A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042623 | ||||||
| chr6:79042750
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+93T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042750 | ||||||
| chr6:79042786
|
A | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.600+57T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042786 | ||||||
| chr6:79043075
|
T | C | 126 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.440-72A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043075 | ||||||
| chr6:79043268
|
A | ATTACTTG others(9): Show |
2 | a0002c0002t0004g0216a0002c0002t0004g0217 | 2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.440-266_440-265ins others(16): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043268 | ||||||
| chr6:79043269
|
A | G | 4 | a0002c0002t0004g0215a0002c0009t0004g0009a0002c0009t0004g0214others(1): Show | 5 | HG00738.hp1 HG01106.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-266T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043269 | ||||||
| chr6:79043308
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-305C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043308 | ||||||
| chr6:79043345
|
C | T | 1 | a0001c0006t0002g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.440-342G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043345 | ||||||
| chr6:79043356
|
G | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.440-353C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043356 | ||||||
| chr6:79043569
|
T | C | 94 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(91): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.440-566A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043569 | ||||||
| chr6:79043677
|
T | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.440-674A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043677 | ||||||
| chr6:79043702
|
TC | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-700delG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043702 | ||||||
| chr6:79043705
|
ATCTAAAT others(19): Show |
A | 3 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0044 | 3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.440-728_440-703del others(26): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043705 | ||||||
| chr6:79043792
|
G | A | 1 | a0002c0002t0003g0243 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.440-789C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043792 | ||||||
| chr6:79043826
|
A | G | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.440-823T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043826 | ||||||
| chr6:79043829
|
C | CT | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.440-827dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043829 | ||||||
| chr6:79043829
|
CT | C | 8 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(5): Show | 8 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-827delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043829 | ||||||
| chr6:79043958
|
C | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-955G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043958 | ||||||
| chr6:79044255
|
G | A | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-1252C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044255 | ||||||
| chr6:79044294
|
T | C | 1 | a0003c0003t0061g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.440-1291A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044294 | ||||||
| chr6:79044377
|
T | A | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.440-1374A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044377 | ||||||
| chr6:79044442
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-1439T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044442 | ||||||
| chr6:79044603
|
A | G | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.440-1600T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044603 | ||||||
| chr6:79044643
|
G | A | 281 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(278): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.440-1640C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044643 | ||||||
| chr6:79044651
|
T | A | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.440-1648A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044651 | ||||||
| chr6:79044757
|
G | A | 1 | a0001c0001t0005g0098 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.440-1754C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044757 | ||||||
| chr6:79044975
|
T | C | 1 | a0002c0002t0062g0199 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.440-1972A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044975 | ||||||
| chr6:79045058
|
T | C | 1 | a0002c0002t0058g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.440-2055A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045058 | ||||||
| chr6:79045170
|
G | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-2167C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045170 | ||||||
| chr6:79045221
|
C | T | 1 | a0002c0002t0063g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.440-2218G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045221 | ||||||
| chr6:79045307
|
T | C | 4 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(1): Show | 4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-2304A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045307 | ||||||
| chr6:79045368
|
A | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-2365T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045368 | ||||||
| chr6:79045536
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.440-2533T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045536 | ||||||
| chr6:79045714
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-2711A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045714 | ||||||
| chr6:79045820
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.440-2817A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045820 | ||||||
| chr6:79045990
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-2987G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045990 | ||||||
| chr6:79046092
|
G | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.440-3089C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046092 | ||||||
| chr6:79046138
|
G | A | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.440-3135C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046138 | ||||||
| chr6:79046238
|
T | C | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.440-3235A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046238 | ||||||
| chr6:79046329
|
C | T | 2 | a0002c0002t0007g0003a0002c0002t0007g0039 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.440-3326G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046329 | ||||||
| chr6:79046371
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-3368A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046371 | ||||||
| chr6:79046375
|
A | T | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.440-3372T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046375 | ||||||
| chr6:79046484
|
A | G | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-3481T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046484 | ||||||
| chr6:79046605
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-3602T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046605 | ||||||
| chr6:79046627
|
A | T | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-3624T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046627 | ||||||
| chr6:79046674
|
C | G | 1 | a0001c0001t0015g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.440-3671G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046674 | ||||||
| chr6:79046776
|
T | G | 2 | a0002c0002t0004g0229a0002c0002t0010g0228 | 2 | NA18612.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.440-3773A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046776 | ||||||
| chr6:79046876
|
A | AAAC | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-3876_440-3874d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046876 | ||||||
| chr6:79046903
|
T | TA | 9 | a0001c0001t0001g0099a0001c0001t0001g0131a0001c0005t0019g0012others(6): Show | 10 | HG01175.hp2 HG01261.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.440-3901dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046903 | ||||||
| chr6:79046903
|
TA | T | 23 | a0001c0001t0001g0103a0001c0001t0001g0111a0001c0001t0005g0077others(20): Show | 23 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.440-3901delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046903 | ||||||
| chr6:79047050
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4047C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047050 | ||||||
| chr6:79047057
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-4054A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047057 | ||||||
| chr6:79047217
|
A | G | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.440-4214T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047217 | ||||||
| chr6:79047227
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4224G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047227 | ||||||
| chr6:79047338
|
C | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.440-4335G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047338 | ||||||
| chr6:79047456
|
T | C | 3 | a0001c0001t0021g0027a0001c0001t0021g0028a0001c0001t0021g0030 | 3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.440-4453A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047456 | ||||||
| chr6:79047637
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4634C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047637 | ||||||
| chr6:79047716
|
T | C | 1 | a0004c0004t0013g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.440-4713A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047716 | ||||||
| chr6:79047721
|
A | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(94): Show | 98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.440-4718T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047721 | ||||||
| chr6:79047756
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.440-4753A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047756 | ||||||
| chr6:79047762
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4759A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047762 | ||||||
| chr6:79047794
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440-4791G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047794 | ||||||
| chr6:79047988
|
T | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-4985A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047988 | ||||||
| chr6:79047998
|
T | C | 1 | a0003c0003t0002g0289 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.440-4995A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047998 | ||||||
| chr6:79048003
|
A | AT | 8 | a0001c0010t0057g0163a0003c0003t0002g0015a0003c0003t0002g0286others(5): Show | 9 | HG00099.hp2 HG01070.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.440-5001dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048003 | ||||||
| chr6:79048273
|
C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.440-5270G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048273 | ||||||
| chr6:79048286
|
G | C | 1 | a0004c0004t0006g0189 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.440-5283C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048286 | ||||||
| chr6:79048289
|
G | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.440-5286C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048289 | ||||||
| chr6:79048450
|
A | T | 42 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(39): Show | 48 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.440-5447T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048450 | ||||||
| chr6:79048501
|
C | A | 126 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.440-5498G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048501 | ||||||
| chr6:79048506
|
T | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.440-5503A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048506 | ||||||
| chr6:79048810
|
A | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-5807T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048810 | ||||||
| chr6:79049121
|
G | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.440-6118C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049121 | ||||||
| chr6:79049149
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.440-6146C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049149 | ||||||
| chr6:79049231
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-6228G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049231 | ||||||
| chr6:79049278
|
T | G | 4 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(1): Show | 7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-6275A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049278 | ||||||
| chr6:79049366
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-6363G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049366 | ||||||
| chr6:79049414
|
C | T | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440-6411G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049414 | ||||||
| chr6:79049587
|
C | T | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.440-6584G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049587 | ||||||
| chr6:79049616
|
G | A | 2 | a0003c0003t0002g0284a0003c0003t0002g0285 | 2 | NA18977.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.440-6613C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049616 | ||||||
| chr6:79049771
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-6768A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049771 | ||||||
| chr6:79049843
|
T | C | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.440-6840A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049843 | ||||||
| chr6:79050010
|
A | G | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.440-7007T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050010 | ||||||
| chr6:79050015
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.440-7012G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050015 | ||||||
| chr6:79050077
|
G | GT | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-7075dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050077 | ||||||
| chr6:79050121
|
C | T | 1 | a0002c0002t0003g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.440-7118G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050121 | ||||||
| chr6:79050259
|
A | G | 1 | a0002c0002t0051g0248 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.440-7256T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050259 | ||||||
| chr6:79050308
|
A | G | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.440-7305T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050308 | ||||||
| chr6:79050445
|
G | A | 3 | a0001c0006t0002g0013a0001c0006t0002g0268a0001c0006t0002g0275 | 4 | NA19011.hp1 NA19057.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-7442C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050445 | ||||||
| chr6:79050556
|
G | A | 1 | a0001c0005t0023g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.440-7553C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050556 | ||||||
| chr6:79050590
|
T | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-7587A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050590 | ||||||
| chr6:79050607
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.440-7604A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050607 | ||||||
| chr6:79050696
|
G | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-7693C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050696 | ||||||
| chr6:79050825
|
C | T | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-7822G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050825 | ||||||
| chr6:79050979
|
C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.440-7976G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050979 | ||||||
| chr6:79051103
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-8100A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051103 | ||||||
| chr6:79051107
|
C | T | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-8104G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051107 | ||||||
| chr6:79051152
|
G | A | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.440-8149C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051152 | ||||||
| chr6:79051266
|
G | C | 8 | a0002c0002t0003g0237a0002c0002t0003g0238a0002c0002t0003g0249others(5): Show | 8 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-8263C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051266 | ||||||
| chr6:79051280
|
C | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.440-8277G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051280 | ||||||
| chr6:79051336
|
G | T | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.440-8333C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051336 | ||||||
| chr6:79051401
|
T | C | 1 | a0001c0001t0034g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.440-8398A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051401 | ||||||
| chr6:79051525
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-8522A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051525 | ||||||
| chr6:79051614
|
G | T | 8 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0003others(5): Show | 10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.440-8611C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051614 | ||||||
| chr6:79051793
|
C | T | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439+8685G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051793 | ||||||
| chr6:79051920
|
G | GT | 17 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(14): Show | 17 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.439+8557dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051920 | ||||||
| chr6:79051920
|
G | T | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.439+8558C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051920 | ||||||
| chr6:79051928
|
T | A | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+8550A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051928 | ||||||
| chr6:79052169
|
T | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+8309A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052169 | ||||||
| chr6:79052196
|
G | A | 4 | a0002c0002t0003g0010a0002c0002t0003g0244a0002c0002t0003g0245others(1): Show | 5 | HG01074.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+8282C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052196 | ||||||
| chr6:79052333
|
T | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+8145A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052333 | ||||||
| chr6:79052428
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.439+8050C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052428 | ||||||
| chr6:79052455
|
G | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.439+8023C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052455 | ||||||
| chr6:79052467
|
T | G | 1 | a0002c0002t0066g0230 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.439+8011A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052467 | ||||||
| chr6:79052488
|
C | T | 4 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019others(1): Show | 4 | HG02698.hp1 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+7990G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052488 | ||||||
| chr6:79052979
|
A | G | 1 | a0001c0001t0005g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.439+7499T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052979 | ||||||
| chr6:79053106
|
G | A | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+7372C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053106 | ||||||
| chr6:79053110
|
T | A | 1 | a0002c0002t0004g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.439+7368A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053110 | ||||||
| chr6:79053183
|
G | A | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.439+7295C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053183 | ||||||
| chr6:79053258
|
G | A | 1 | a0004c0004t0006g0181 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.439+7220C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053258 | ||||||
| chr6:79053263
|
G | A | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+7215C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053263 | ||||||
| chr6:79053271
|
G | A | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.439+7207C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053271 | ||||||
| chr6:79053549
|
G | C | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.439+6929C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053549 | ||||||
| chr6:79053599
|
G | A | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.439+6879C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053599 | ||||||
| chr6:79053647
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+6831G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053647 | ||||||
| chr6:79053655
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+6823A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053655 | ||||||
| chr6:79053739
|
T | C | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439+6739A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053739 | ||||||
| chr6:79053877
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0108a0001c0001t0005g0076others(2): Show | 5 | NA18950.hp1 NA18975.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+6601G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053877 | ||||||
| chr6:79053980
|
G | A | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.439+6498C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053980 | ||||||
| chr6:79054103
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+6375T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054103 | ||||||
| chr6:79054342
|
C | CA | 119 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(116): Show | 120 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.439+6135dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054342 | ||||||
| chr6:79054386
|
T | C | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.439+6092A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054386 | ||||||
| chr6:79054595
|
C | T | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.439+5883G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054595 | ||||||
| chr6:79054650
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.439+5828G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054650 | ||||||
| chr6:79054739
|
C | A | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.439+5739G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054739 | ||||||
| chr6:79054739
|
C | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+5739G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054739 | ||||||
| chr6:79054898
|
C | T | 283 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(280): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.439+5580G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054898 | ||||||
| chr6:79054943
|
C | CT | 83 | a0001c0005t0038g0047a0001c0005t0045g0046a0001c0010t0057g0163others(80): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.439+5534dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054943 | ||||||
| chr6:79054956
|
T | TA | 4 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(1): Show | 4 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+5521dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054956 | ||||||
| chr6:79055163
|
G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.439+5315C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055163 | ||||||
| chr6:79055377
|
T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.439+5101A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055377 | ||||||
| chr6:79055444
|
G | A | 1 | a0001c0001t0011g0255 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.439+5034C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055444 | ||||||
| chr6:79055478
|
T | A | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.439+5000A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055478 | ||||||
| chr6:79055624
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.439+4854A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055624 | ||||||
| chr6:79055668
|
G | A | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.439+4810C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055668 | ||||||
| chr6:79056227
|
G | A | 8 | a0002c0002t0003g0041a0002c0002t0003g0042a0002c0002t0007g0003others(5): Show | 10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.439+4251C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056227 | ||||||
| chr6:79056366
|
G | A | 4 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(1): Show | 4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+4112C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056366 | ||||||
| chr6:79056479
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.439+3999C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056479 | ||||||
| chr6:79056486
|
G | T | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+3992C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056486 | ||||||
| chr6:79056541
|
C | T | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.439+3937G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056541 | ||||||
| chr6:79056649
|
A | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+3829T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056649 | ||||||
| chr6:79056657
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.439+3821G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056657 | ||||||
| chr6:79056699
|
T | A | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.439+3779A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056699 | ||||||
| chr6:79056834
|
A | G | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+3644T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056834 | ||||||
| chr6:79056878
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0146a0001c0001t0005g0145 | 3 | NA18612.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.439+3600T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056878 | ||||||
| chr6:79056883
|
T | G | 1 | a0001c0001t0005g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.439+3595A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056883 | ||||||
| chr6:79057010
|
G | A | 1 | a0001c0001t0005g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.439+3468C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057010 | ||||||
| chr6:79057060
|
T | C | 29 | a0001c0001t0011g0029a0001c0001t0011g0150a0001c0001t0011g0151others(26): Show | 29 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.439+3418A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057060 | ||||||
| chr6:79057300
|
A | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.439+3178T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057300 | ||||||
| chr6:79057306
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.439+3172G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057306 | ||||||
| chr6:79057597
|
G | A | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439+2881C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057597 | ||||||
| chr6:79057714
|
T | C | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.439+2764A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057714 | ||||||
| chr6:79057757
|
C | T | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439+2721G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057757 | ||||||
| chr6:79058113
|
G | A | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+2365C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058113 | ||||||
| chr6:79058186
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.439+2292C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058186 | ||||||
| chr6:79058368
|
T | TGTCA | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+2106_439+2109d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058368 | ||||||
| chr6:79058641
|
T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.439+1837A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058641 | ||||||
| chr6:79058855
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18960.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.439+1623A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058855 | ||||||
| chr6:79058884
|
C | T | 2 | a0001c0005t0054g0038a0001c0005t0055g0045 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439+1594G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058884 | ||||||
| chr6:79059225
|
T | C | 1 | a0001c0001t0005g0299 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.439+1253A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059225 | ||||||
| chr6:79059339
|
A | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.439+1139T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059339 | ||||||
| chr6:79059473
|
A | G | 2 | a0002c0002t0003g0193a0002c0002t0008g0197 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.439+1005T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059473 | ||||||
| chr6:79059591
|
T | TTA | 36 | a0001c0001t0021g0027a0001c0008t0007g0171a0002c0002t0003g0011others(33): Show | 37 | HG00558.hp1 HG00673.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.439+885_439+886dup others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATA | 22 | a0001c0001t0011g0029a0001c0001t0021g0028a0001c0001t0021g0030others(19): Show | 27 | HG00621.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.439+883_439+886dup others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATA | 6 | a0001c0010t0029g0054a0002c0002t0010g0234a0002c0002t0027g0239others(3): Show | 6 | HG00738.hp1 HG01978.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+881_439+886dup others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(1): Show |
7 | a0001c0001t0015g0156a0001c0001t0017g0023a0001c0001t0017g0031others(4): Show | 7 | HG01358.hp2 HG01891.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+879_439+886dup others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0014g0161a0001c0001t0015g0159a0008c0019t0013g0190 | 3 | HG00639.hp1 HG03654.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.439+877_439+886dup others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(5): Show |
6 | a0001c0001t0011g0150a0001c0001t0014g0160a0001c0001t0015g0157others(3): Show | 6 | HG00280.hp2 HG01175.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+875_439+886dup others(12): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(7): Show |
10 | a0001c0001t0011g0151a0001c0001t0011g0256a0001c0001t0014g0162others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.439+873_439+886dup others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0011g0255 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.439+871_439+886dup others(16): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(11): Show |
6 | a0001c0001t0011g0153a0001c0007t0012g0173a0001c0007t0012g0174others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+869_439+886dup others(18): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATATAT others(13): Show |
2 | a0001c0007t0012g0177a0001c0010t0057g0163 | 2 | HG01358.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.439+867_439+886dup others(20): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
T | TTATTTAT others(11): Show |
1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439+886_439+887ins others(18): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
TTA | T | 13 | a0001c0006t0002g0269a0001c0006t0002g0270a0001c0006t0002g0275others(10): Show | 14 | HG00099.hp2 HG01109.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.439+885_439+886del others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
TTATA | T | 29 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(26): Show | 35 | HG00438.hp2 HG00735.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.439+883_439+886del others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
TTATATA | T | 4 | a0001c0006t0002g0267a0001c0006t0002g0271a0001c0006t0009g0297others(1): Show | 4 | HG01123.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+881_439+886del others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
TTATATAT others(3): Show |
T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439+877_439+886del others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
TTATATAT others(7): Show |
T | 4 | a0002c0002t0007g0003a0002c0002t0007g0004a0002c0002t0007g0039others(1): Show | 6 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+873_439+886del others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059591
|
TTATATAT others(9): Show |
T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+871_439+886del others(16): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | ||||||
| chr6:79059595
|
A | T | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439+883T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059595 | ||||||
| chr6:79059608
|
TATATATA others(11): Show |
T | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+852_439+869del others(18): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059608 | ||||||
| chr6:79059612
|
TATATATA others(7): Show |
T | 4 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(1): Show | 4 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+852_439+865del others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059612 | ||||||
| chr6:79059614
|
TATATATA others(5): Show |
T | 4 | a0001c0001t0014g0158a0001c0001t0015g0155a0001c0005t0038g0047others(1): Show | 4 | HG02818.hp1 HG02886.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+852_439+863del others(12): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059614 | ||||||
| chr6:79059616
|
TATATATA others(3): Show |
T | 5 | a0001c0001t0059g0118a0001c0005t0019g0012a0001c0005t0019g0264others(2): Show | 6 | HG02559.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+852_439+861del others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059616 | ||||||
| chr6:79059618
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0005t0055g0045 | 3 | HG03225.hp1 NA18991.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.439+852_439+859del others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059618 | ||||||
| chr6:79059620
|
TATATAA | T | 77 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(74): Show | 78 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.439+852_439+857del others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059620 | ||||||
| chr6:79059622
|
TATAA | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0119others(6): Show | 9 | HG01074.hp1 HG01496.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+852_439+855del others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059622 | ||||||
| chr6:79059624
|
TAA | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(5): Show | 8 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+852_439+853del others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059624 | ||||||
| chr6:79059626
|
A | T | 25 | a0001c0001t0011g0029a0001c0001t0011g0150a0001c0001t0011g0151others(22): Show | 27 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.439+852T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059626 | ||||||
| chr6:79059627
|
A | T | 1 | a0001c0001t0025g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.439+851T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059627 | ||||||
| chr6:79059851
|
T | C | 1 | a0002c0002t0003g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.439+627A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059851 | ||||||
| chr6:79059884
|
G | A | 3 | a0001c0005t0049g0036a0001c0005t0054g0038a0001c0005t0055g0045 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.439+594C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059884 | ||||||
| chr6:79059997
|
G | C | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+481C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059997 | ||||||
| chr6:79060106
|
GA | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(274): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.439+371delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060106 | ||||||
| chr6:79060140
|
A | G | 7 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+338T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060140 | ||||||
| chr6:79060193
|
T | C | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.439+285A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060193 | ||||||
| chr6:79060234
|
T | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439+244A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060234 | ||||||
| chr6:79060298
|
T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.439+180A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060298 | ||||||
| chr6:79060635
|
T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.340+33A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 5/39 | chr6 | 79060635 | ||||||
| chr6:79060638
|
T | A | 1 | a0002c0002t0022g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.340+30A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 5/39 | chr6 | 79060638 | ||||||
| chr6:79060651
|
T | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340+17A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 5/39 | chr6 | 79060651 | ||||||
| chr6:79060927
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-109C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79060927 | ||||||
| chr6:79060963
|
A | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190-145T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79060963 | ||||||
| chr6:79061058
|
C | T | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.190-240G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061058 | ||||||
| chr6:79061136
|
G | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-318C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061136 | ||||||
| chr6:79061204
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-386A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061204 | ||||||
| chr6:79061489
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.190-671T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061489 | ||||||
| chr6:79061614
|
T | C | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-796A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061614 | ||||||
| chr6:79061842
|
G | T | 1 | a0003c0003t0002g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.190-1024C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061842 | ||||||
| chr6:79061912
|
CCATGAAT others(10): Show |
C | 2 | a0001c0005t0049g0036a0001c0005t0054g0038 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.190-1111_190-1095d others(19): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061912 | ||||||
| chr6:79062158
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-1340A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062158 | ||||||
| chr6:79062257
|
C | T | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1439G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062257 | ||||||
| chr6:79062584
|
T | A | 3 | a0001c0006t0002g0265a0001c0006t0009g0266a0001c0006t0009g0297 | 3 | HG01891.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.190-1766A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062584 | ||||||
| chr6:79062633
|
T | C | 2 | a0001c0001t0026g0149a0001c0001t0026g0154 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190-1815A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062633 | ||||||
| chr6:79062636
|
T | G | 94 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(91): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.190-1818A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062636 | ||||||
| chr6:79062834
|
T | C | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.190-2016A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062834 | ||||||
| chr6:79062852
|
A | AC | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-2035dupG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062852 | ||||||
| chr6:79062931
|
T | G | 2 | a0002c0002t0007g0004a0002c0002t0007g0040 | 3 | HG00099.hp1 HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.190-2113A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062931 | ||||||
| chr6:79062968
|
G | A | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-2150C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062968 | ||||||
| chr6:79063067
|
C | T | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.190-2249G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063067 | ||||||
| chr6:79063087
|
A | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.190-2269T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063087 | ||||||
| chr6:79063136
|
C | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-2318G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063136 | ||||||
| chr6:79063191
|
T | C | 1 | a0001c0001t0014g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.190-2373A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063191 | ||||||
| chr6:79063302
|
G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.190-2484C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063302 | ||||||
| chr6:79063377
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-2559A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063377 | ||||||
| chr6:79063389
|
G | A | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.190-2571C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063389 | ||||||
| chr6:79063529
|
G | C | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-2711C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063529 | ||||||
| chr6:79063636
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-2818G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063636 | ||||||
| chr6:79063660
|
G | A | 1 | a0001c0001t0018g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-2842C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063660 | ||||||
| chr6:79064097
|
C | T | 1 | a0001c0001t0005g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.190-3279G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064097 | ||||||
| chr6:79064432
|
T | C | 1 | a0003c0003t0002g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.190-3614A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064432 | ||||||
| chr6:79064630
|
A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.190-3812T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064630 | ||||||
| chr6:79064708
|
T | C | 1 | a0004c0004t0006g0189 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.190-3890A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064708 | ||||||
| chr6:79064912
|
T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.190-4094A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064912 | ||||||
| chr6:79065195
|
T | G | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-4377A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065195 | ||||||
| chr6:79065201
|
A | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-4383T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065201 | ||||||
| chr6:79065331
|
G | C | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.190-4513C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065331 | ||||||
| chr6:79065764
|
C | CCA | 66 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(63): Show | 73 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.190-4948_190-4947d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
C | CCACA | 15 | a0001c0001t0001g0115a0001c0001t0005g0114a0001c0005t0027g0033others(12): Show | 15 | HG01109.hp2 HG01255.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-4950_190-4947d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
C | CCACACA | 3 | a0001c0001t0001g0139a0001c0001t0005g0116a0003c0003t0002g0295 | 3 | HG02080.hp1 HG03540.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.190-4952_190-4947d others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
C | CCACACAC others(5): Show |
1 | a0002c0002t0003g0011 | 2 | NA18998.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.190-4958_190-4947d others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
CCA | C | 32 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0120others(29): Show | 35 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.190-4948_190-4947d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
CCACA | C | 55 | a0001c0001t0001g0066a0001c0001t0001g0146a0001c0001t0005g0145others(52): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.190-4950_190-4947d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
CCACACA | C | 10 | a0001c0001t0001g0119a0001c0001t0059g0118a0002c0002t0003g0201others(7): Show | 10 | HG02080.hp2 HG02559.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.190-4952_190-4947d others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
CCACACAC others(1): Show |
C | 7 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0192others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-4954_190-4947d others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065764
|
CCACACAC others(3): Show |
C | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.190-4956_190-4947d others(12): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | ||||||
| chr6:79065892
|
T | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-5074A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065892 | ||||||
| chr6:79065978
|
T | C | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-5160A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065978 | ||||||
| chr6:79065979
|
A | T | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.190-5161T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065979 | ||||||
| chr6:79066110
|
A | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-5292T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066110 | ||||||
| chr6:79066161
|
C | T | 6 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-5343G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066161 | ||||||
| chr6:79066275
|
T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.190-5457A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066275 | ||||||
| chr6:79066286
|
C | A | 1 | a0001c0001t0069g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.190-5468G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066286 | ||||||
| chr6:79066387
|
A | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.190-5569T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066387 | ||||||
| chr6:79066446
|
A | G | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.190-5628T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066446 | ||||||
| chr6:79066529
|
T | A | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190-5711A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066529 | ||||||
| chr6:79066670
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-5852A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066670 | ||||||
| chr6:79066848
|
C | T | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-6030G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066848 | ||||||
| chr6:79066890
|
G | A | 1 | a0004c0004t0013g0166 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.190-6072C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066890 | ||||||
| chr6:79066994
|
T | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-6176A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066994 | ||||||
| chr6:79067140
|
G | T | 1 | a0001c0001t0011g0255 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.190-6322C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067140 | ||||||
| chr6:79067175
|
C | T | 5 | a0001c0001t0017g0023a0001c0001t0017g0026a0001c0001t0017g0031others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-6357G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067175 | ||||||
| chr6:79067525
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-6707T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067525 | ||||||
| chr6:79067716
|
G | A | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.190-6898C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067716 | ||||||
| chr6:79067764
|
G | C | 1 | a0001c0007t0047g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.190-6946C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067764 | ||||||
| chr6:79067944
|
C | T | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-7126G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067944 | ||||||
| chr6:79068043
|
T | C | 1 | a0002c0002t0003g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.190-7225A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068043 | ||||||
| chr6:79068333
|
C | T | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.190-7515G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068333 | ||||||
| chr6:79068385
|
C | T | 1 | a0001c0011t0016g0018 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.190-7567G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068385 | ||||||
| chr6:79068662
|
G | A | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.190-7844C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068662 | ||||||
| chr6:79069029
|
A | G | 1 | a0002c0002t0004g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.190-8211T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069029 | ||||||
| chr6:79069098
|
T | C | 1 | a0004c0004t0006g0189 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.190-8280A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069098 | ||||||
| chr6:79069107
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-8289A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069107 | ||||||
| chr6:79069267
|
C | T | 7 | a0001c0001t0001g0147a0001c0001t0001g0300a0001c0001t0005g0062others(4): Show | 7 | HG00621.hp2 HG01952.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+8181G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069267 | ||||||
| chr6:79069361
|
G | T | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189+8087C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069361 | ||||||
| chr6:79069416
|
C | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.189+8032G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069416 | ||||||
| chr6:79069464
|
A | G | 8 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(5): Show | 11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+7984T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069464 | ||||||
| chr6:79069611
|
T | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189+7837A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069611 | ||||||
| chr6:79069743
|
C | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189+7705G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069743 | ||||||
| chr6:79069813
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+7635A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069813 | ||||||
| chr6:79069855
|
A | AC | 9 | a0001c0007t0012g0172a0001c0007t0012g0173a0001c0007t0012g0174others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.189+7592_189+7593i others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069855 | ||||||
| chr6:79070050
|
T | G | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(28): Show | 31 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.189+7398A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070050 | ||||||
| chr6:79070374
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+7074T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070374 | ||||||
| chr6:79070850
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+6598T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070850 | ||||||
| chr6:79070857
|
T | C | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+6591A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070857 | ||||||
| chr6:79070859
|
T | C | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+6589A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070859 | ||||||
| chr6:79071067
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+6381G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071067 | ||||||
| chr6:79071109
|
C | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+6339G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071109 | ||||||
| chr6:79071172
|
T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189+6276A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071172 | ||||||
| chr6:79071313
|
GA | G | 4 | a0001c0001t0011g0255a0001c0001t0011g0256a0001c0001t0018g0257others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+6134delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071313 | ||||||
| chr6:79071379
|
T | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+6069A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071379 | ||||||
| chr6:79071496
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+5952A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071496 | ||||||
| chr6:79071578
|
T | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0141a0001c0001t0005g0140others(1): Show | 5 | HG02257.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+5870A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071578 | ||||||
| chr6:79071608
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189+5840C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071608 | ||||||
| chr6:79071841
|
G | A | 1 | a0001c0001t0017g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.189+5607C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071841 | ||||||
| chr6:79071897
|
CTAT | C | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+5548_189+5550d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071897 | ||||||
| chr6:79072072
|
A | T | 1 | a0001c0001t0017g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189+5376T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072072 | ||||||
| chr6:79072188
|
C | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+5260G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072188 | ||||||
| chr6:79072293
|
C | G | 4 | a0001c0005t0027g0033a0001c0006t0008g0037a0001c0012t0024g0034others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+5155G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072293 | ||||||
| chr6:79072388
|
C | T | 1 | a0001c0011t0016g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.189+5060G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072388 | ||||||
| chr6:79072438
|
T | C | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189+5010A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072438 | ||||||
| chr6:79072481
|
A | AT | 134 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.189+4966dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072481 | ||||||
| chr6:79072615
|
T | C | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.189+4833A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072615 | ||||||
| chr6:79072643
|
C | T | 5 | a0001c0008t0003g0170a0001c0008t0007g0167a0001c0008t0007g0168others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4805G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072643 | ||||||
| chr6:79072738
|
C | T | 3 | a0001c0006t0002g0014a0001c0006t0002g0269a0001c0006t0002g0270 | 4 | HG02258.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+4710G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072738 | ||||||
| chr6:79072740
|
G | C | 2 | a0001c0001t0014g0160a0001c0001t0015g0159 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.189+4708C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072740 | ||||||
| chr6:79072800
|
A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189+4648T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072800 | ||||||
| chr6:79072819
|
T | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+4629A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072819 | ||||||
| chr6:79072854
|
C | T | 2 | a0001c0006t0002g0013a0001c0006t0002g0268 | 3 | NA19011.hp1 NA19057.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.189+4594G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072854 | ||||||
| chr6:79072891
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+4557T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072891 | ||||||
| chr6:79072928
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.189+4520A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072928 | ||||||
| chr6:79072942
|
C | A | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+4506G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072942 | ||||||
| chr6:79073116
|
T | A | 1 | a0004c0004t0006g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.189+4332A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073116 | ||||||
| chr6:79073157
|
T | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.189+4291A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073157 | ||||||
| chr6:79073178
|
A | AT | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+4269_189+4270i others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073178 | ||||||
| chr6:79073197
|
T | C | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+4251A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073197 | ||||||
| chr6:79073226
|
A | C | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.189+4222T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073226 | ||||||
| chr6:79073298
|
T | C | 1 | a0002c0002t0007g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.189+4150A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073298 | ||||||
| chr6:79073319
|
CGCCTA | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4124_189+4128d others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073319 | ||||||
| chr6:79073320
|
G | A | 293 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(290): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.189+4128C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073320 | ||||||
| chr6:79073327
|
A | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4121T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073327 | ||||||
| chr6:79073549
|
A | C | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+3899T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073549 | ||||||
| chr6:79073560
|
TATG | T | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+3885_189+3887d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073560 | ||||||
| chr6:79073630
|
C | T | 7 | a0002c0002t0003g0193a0002c0002t0003g0195a0002c0002t0008g0192others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+3818G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073630 | ||||||
| chr6:79073650
|
C | A | 1 | a0003c0003t0002g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.189+3798G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073650 | ||||||
| chr6:79073978
|
C | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189+3470G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073978 | ||||||
| chr6:79074096
|
A | G | 11 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(8): Show | 14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+3352T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074096 | ||||||
| chr6:79074263
|
G | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189+3185C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074263 | ||||||
| chr6:79074381
|
T | C | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.189+3067A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074381 | ||||||
| chr6:79074427
|
G | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+3021C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074427 | ||||||
| chr6:79074431
|
T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+3017A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074431 | ||||||
| chr6:79074557
|
T | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2891A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074557 | ||||||
| chr6:79074640
|
T | C | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189+2808A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074640 | ||||||
| chr6:79074678
|
C | T | 4 | a0001c0006t0002g0265a0001c0006t0002g0267a0001c0006t0009g0266others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+2770G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074678 | ||||||
| chr6:79074704
|
G | C | 80 | a0002c0002t0003g0010a0002c0002t0003g0011a0002c0002t0003g0041others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.189+2744C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074704 | ||||||
| chr6:79074849
|
A | C | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2599T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074849 | ||||||
| chr6:79075013
|
C | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2435G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075013 | ||||||
| chr6:79075146
|
G | T | 19 | a0001c0001t0011g0150a0001c0001t0011g0151a0001c0001t0011g0153others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+2302C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075146 | ||||||
| chr6:79075165
|
A | T | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2283T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075165 | ||||||
| chr6:79075334
|
G | A | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+2114C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075334 | ||||||
| chr6:79075355
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0005g0145 | 2 | NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.189+2093C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075355 | ||||||
| chr6:79075378
|
A | G | 2 | a0001c0006t0020g0006a0001c0006t0020g0148 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.189+2070T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075378 | ||||||
| chr6:79075419
|
G | A | 2 | a0001c0012t0024g0034a0001c0015t0024g0035 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189+2029C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075419 | ||||||
| chr6:79075422
|
C | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2026G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075422 | ||||||
| chr6:79075604
|
C | T | 2 | a0001c0001t0037g0055a0001c0001t0044g0056 | 2 | HG00639.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.189+1844G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075604 | ||||||
| chr6:79075634
|
G | GA | 6 | a0001c0001t0001g0147a0001c0001t0011g0255a0001c0001t0011g0256others(3): Show | 6 | HG00738.hp1 HG02258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1813dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075634 | ||||||
| chr6:79075634
|
GA | G | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+1813delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075634 | ||||||
| chr6:79075635
|
A | G | 1 | a0003c0003t0002g0032 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.189+1813T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075635 | ||||||
| chr6:79075645
|
C | A | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+1803G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075645 | ||||||
| chr6:79075669
|
CGAG | C | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+1776_189+1778d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075669 | ||||||
| chr6:79075695
|
G | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+1753C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075695 | ||||||
| chr6:79075812
|
A | C | 3 | a0001c0006t0002g0265a0001c0006t0009g0266a0001c0006t0009g0297 | 3 | HG01891.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.189+1636T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075812 | ||||||
| chr6:79075890
|
C | T | 106 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(103): Show | 107 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.189+1558G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075890 | ||||||
| chr6:79075949
|
A | T | 1 | a0001c0005t0046g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+1499T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075949 | ||||||
| chr6:79076216
|
C | A | 2 | a0002c0002t0028g0260a0002c0002t0028g0261 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.189+1232G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076216 | ||||||
| chr6:79076228
|
C | T | 2 | a0001c0010t0029g0053a0001c0010t0029g0054 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+1220G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076228 | ||||||
| chr6:79076494
|
C | G | 3 | a0001c0005t0027g0033a0001c0012t0024g0034a0001c0015t0024g0035 | 3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189+954G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076494 | ||||||
| chr6:79076617
|
C | T | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189+831G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076617 | ||||||
| chr6:79076695
|
C | T | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+753G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076695 | ||||||
| chr6:79076761
|
C | T | 6 | a0001c0005t0023g0049a0001c0005t0023g0051a0001c0005t0030g0048others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+687G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076761 | ||||||
| chr6:79076922
|
A | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+526T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076922 | ||||||
| chr6:79076922
|
A | G | 18 | a0001c0005t0003g0001a0001c0005t0019g0012a0001c0005t0019g0264others(15): Show | 23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.189+526T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076922 | ||||||
| chr6:79076928
|
A | C | 40 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(37): Show | 46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.189+520T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076928 | ||||||
| chr6:79077070
|
G | A | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.189+378C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077070 | ||||||
| chr6:79077074
|
G | C | 1 | a0002c0002t0003g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.189+374C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077074 | ||||||
| chr6:79077091
|
C | T | 9 | a0001c0001t0011g0029a0001c0001t0017g0023a0001c0001t0017g0026others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+357G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077091 | ||||||
| chr6:79077265
|
A | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+183T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077265 | ||||||
| chr6:79077277
|
C | A | 3 | a0001c0005t0019g0012a0001c0005t0019g0264a0001c0005t0046g0263 | 4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+171G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077277 | ||||||
| chr6:79077279
|
C | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.189+169G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077279 | ||||||
| chr6:79077524
|
C | A | 1 | a0003c0003t0052g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.130-17G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 3/39 | chr6 | 79077524 | ||||||
| chr6:79077621
|
C | G | 3 | a0001c0011t0016g0017a0001c0011t0016g0018a0001c0011t0016g0019 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.129+79G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 3/39 | chr6 | 79077621 | ||||||
| chr6:79077739
|
C | T | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.100-10G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 2/39 | chr6 | 79077739 | ||||||
| chr6:79077772
|
C | T | 1 | a0002c0002t0048g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100-43G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 2/39 | chr6 | 79077772 | ||||||
| chr6:79077779
|
C | CCCG | 4 | a0001c0001t0033g0021a0001c0011t0016g0017a0001c0011t0016g0018others(1): Show | 4 | HG00280.hp2 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-53_100-51dupCG others(1): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 2/39 | chr6 | 79077779 | ||||||
| chr6:79077938
|
G | A | 39 | a0001c0006t0002g0013a0001c0006t0002g0014a0001c0006t0002g0265others(36): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.41-25C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/39 | chr6 | 79077938 | ||||||
| chr6:79077945
|
A | T | 1 | a0002c0002t0048g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-32T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/39 | chr6 | 79077945 | ||||||
| chr6:79077973
|
G | A | 2 | a0001c0001t0001g0300a0001c0001t0005g0299 | 2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.40+56C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/39 | chr6 | 79077973 |