Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5727 |
|---|---|
| ensemblid | ENSG00000185920.19 |
| hgncid | 9585 |
| symbol | PTCH1 |
| name | patched 1 |
| refseq_nuc | NM_000264.5 |
| refseq_prot | NP_000255.2 |
| ensembl_nuc | ENST00000331920.11 |
| ensembl_prot | ENSP00000332353.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 95442980 |
| end | 95509266 |
| strand | - |
| ver | v1.2 |
| region | chr9:95442980-95509266 |
| region5000 | chr9:95437980-95514266 |
| regionname0 | PTCH1_chr9_95442980_95509266 |
| regionname5000 | PTCH1_chr9_95437980_95514266 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1447 | 152 | 53 | 28 | 45 | 8 | 17 | 37 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002 | 0/1 | 1447 | 84 | 18 | 12 | 44 | 4 | 5 | 31 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003 | 0/0 | 1447 | 24 | 9 | 0 | 13 | 0 | 2 | 8 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004 | 0/0 | 1447 | 7 | 0 | 0 | 6 | 0 | 1 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0005 | 0/0 | 1447 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0006 | 0/0 | 1447 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0007 | 0/0 | 1447 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0008 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0009 | 0/0 | 1447 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0010 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0011 | 0/0 | 1447 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0012 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0013 | 0/0 | 1447 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0014 | 0/0 | 1447 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0015 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0016 | 0/0 | 1447 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4344 | 74 | 15 | 12 | 39 | 3 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0002 | 1/0 | 4344 | 65 | 27 | 18 | 8 | 3 | 8 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0003 | 0/0 | 4344 | 45 | 19 | 5 | 17 | 2 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0004 | 0/0 | 4344 | 25 | 1 | 2 | 16 | 2 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0005 | 0/0 | 4344 | 20 | 9 | 0 | 9 | 0 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0006 | 0/0 | 4344 | 6 | 0 | 0 | 5 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0007 | 0/0 | 4344 | 4 | 0 | 0 | 3 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0008 | 0/0 | 4344 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0009 | 0/0 | 4344 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0010 | 0/0 | 4344 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0011 | 0/0 | 4344 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0012 | 0/0 | 4344 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0013 | 0/0 | 4344 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0014 | 0/0 | 4344 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0015 | 0/0 | 4344 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0016 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0017 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0018 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0019 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0020 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0021 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0022 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0023 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0024 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0025 | 0/0 | 4344 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0026 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0027 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0028 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0029 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0030 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0031 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0032 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0033 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0034 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0035 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0036 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0037 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0038 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| c0039 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4318 | 85 | 5 | 17 | 46 | 3 | 12 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0002 | 0/0 | 4321 | 41 | 5 | 3 | 25 | 2 | 6 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0003 | 0/0 | 4318 | 29 | 8 | 8 | 7 | 2 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0004 | 0/0 | 4324 | 23 | 1 | 4 | 14 | 2 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0005 | 0/0 | 4321 | 12 | 9 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0006 | 0/0 | 4321 | 9 | 6 | 1 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0007 | 0/0 | 4328 | 7 | 6 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0008 | 0/0 | 4320 | 6 | 6 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0009 | 0/0 | 4325 | 5 | 5 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0010 | 0/0 | 4319 | 5 | 5 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0011 | 0/0 | 4324 | 5 | 1 | 0 | 4 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0012 | 0/0 | 4315 | 4 | 2 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0013 | 0/0 | 4319 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0014 | 0/0 | 4322 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0015 | 0/0 | 4322 | 3 | 2 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0016 | 0/0 | 4319 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0017 | 0/0 | 4318 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0018 | 0/0 | 4324 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0019 | 0/0 | 4318 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0020 | 0/0 | 4319 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0021 | 0/0 | 4327 | 2 | 0 | 1 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0022 | 0/0 | 4306 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0023 | 0/0 | 4323 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0024 | 0/0 | 4321 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0025 | 0/0 | 4322 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0026 | 0/0 | 4318 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0027 | 0/0 | 4319 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0028 | 0/0 | 4329 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0029 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0030 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0031 | 0/0 | 4318 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0032 | 0/0 | 4318 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0033 | 0/0 | 4319 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0034 | 0/0 | 4319 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0035 | 0/0 | 4319 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0036 | 0/0 | 4321 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0037 | 0/0 | 4325 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0038 | 0/0 | 4319 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0039 | 0/0 | 4321 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0040 | 0/0 | 4321 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0041 | 0/0 | 4322 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0042 | 0/0 | 4327 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0043 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0044 | 0/0 | 4307 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0045 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0046 | 0/0 | 4321 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0047 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| t0048 | 0/0 | 4321 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 4344 | 65 | 27 | 18 | 8 | 3 | 8 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003 | 0/0 | 4344 | 45 | 19 | 5 | 17 | 2 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004 | 0/0 | 4344 | 25 | 1 | 2 | 16 | 2 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0007 | 0/0 | 4344 | 4 | 0 | 0 | 3 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0009 | 0/0 | 4344 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0013 | 0/0 | 4344 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0014 | 0/0 | 4344 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0022 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0024 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0030 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0037 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0038 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001 | 0/1 | 4344 | 74 | 15 | 12 | 39 | 3 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0011 | 0/0 | 4344 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0017 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0019 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0020 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0029 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0032 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0035 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0036 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005 | 0/0 | 4344 | 20 | 9 | 0 | 9 | 0 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0010 | 0/0 | 4344 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0031 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004c0006 | 0/0 | 4344 | 6 | 0 | 0 | 5 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004c0021 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0005c0008 | 0/0 | 4344 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0006c0016 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0006c0023 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0007c0012 | 0/0 | 4344 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0008c0039 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0009c0015 | 0/0 | 4344 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0010c0018 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0011c0025 | 0/0 | 4344 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0012c0028 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0013c0027 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0014c0026 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0015c0033 | 0/0 | 4344 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0016c0034 | 0/0 | 4344 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 1/0 | 8661 | 15 | 0 | 5 | 3 | 1 | 5 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0002 | 0/0 | 8664 | 3 | 2 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0003 | 0/0 | 8661 | 16 | 2 | 5 | 4 | 2 | 3 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0005 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0006 | 0/0 | 8664 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0007 | 0/0 | 8671 | 7 | 6 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0008 | 0/0 | 8663 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0010 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0011 | 0/0 | 8667 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0012 | 0/0 | 8658 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0015 | 0/0 | 8665 | 3 | 2 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0016 | 0/0 | 8662 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0021 | 0/0 | 8670 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0023 | 0/0 | 8666 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0034 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0037 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0040 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0046 | 0/0 | 8664 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0002t0048 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0001 | 0/0 | 8661 | 4 | 0 | 1 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0002 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0004 | 0/0 | 8667 | 20 | 1 | 4 | 12 | 1 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0005 | 0/0 | 8664 | 5 | 4 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0008 | 0/0 | 8663 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0012 | 0/0 | 8658 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0013 | 0/0 | 8662 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0020 | 0/0 | 8662 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0031 | 0/0 | 8661 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0035 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0003t0042 | 0/0 | 8670 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004t0001 | 0/0 | 8661 | 5 | 1 | 0 | 1 | 1 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004t0002 | 0/0 | 8664 | 14 | 0 | 1 | 10 | 1 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004t0006 | 0/0 | 8664 | 3 | 0 | 1 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004t0021 | 0/0 | 8670 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004t0024 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0004t0039 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0007t0002 | 0/0 | 8664 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0007t0022 | 0/0 | 8649 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0009t0002 | 0/0 | 8664 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0013t0025 | 0/0 | 8665 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0014t0003 | 0/0 | 8661 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0014t0038 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0022t0002 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0024t0006 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0030t0043 | 0/0 | 8670 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0037t0002 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0001c0038t0044 | 0/0 | 8650 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0001 | 0/1 | 8661 | 50 | 3 | 10 | 32 | 1 | 3 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0003 | 0/0 | 8661 | 3 | 0 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0004 | 0/0 | 8667 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0005 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0009 | 0/0 | 8668 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0017 | 0/0 | 8661 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0018 | 0/0 | 8667 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0019 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0026 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0027 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0028 | 0/0 | 8672 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0029 | 0/0 | 8667 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0030 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0032 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0001t0047 | 0/0 | 8671 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0011t0002 | 0/0 | 8664 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0017t0004 | 0/0 | 8667 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0019t0009 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0020t0001 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0029t0001 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0032t0001 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0035t0001 | 0/0 | 8661 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0002c0036t0036 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0001 | 0/0 | 8661 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0002 | 0/0 | 8664 | 6 | 0 | 0 | 5 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0003 | 0/0 | 8661 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0005 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0006 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0011 | 0/0 | 8667 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0024 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0005t0041 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0010t0014 | 0/0 | 8665 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0010t0033 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0003c0031t0003 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004c0006t0001 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004c0006t0002 | 0/0 | 8664 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004c0006t0005 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0004c0021t0014 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0005c0008t0010 | 0/0 | 8662 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0006c0016t0001 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0006c0023t0011 | 0/0 | 8667 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0007c0012t0003 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0008c0039t0001 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0009c0015t0001 | 0/0 | 8661 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0010c0018t0022 | 0/0 | 8649 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0011c0025t0003 | 0/0 | 8661 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0012c0028t0002 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0013c0027t0001 | 0/0 | 8661 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0014c0026t0045 | 0/0 | 8671 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0015c0033t0005 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| a0016c0034t0003 | 0/0 | 8661 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | copy fasta | chr9 | 95437980 | 95514266 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0012g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0015g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0021g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0023g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0023g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0034g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0037g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0040g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0046g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0048g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0020g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0020g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0031g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0035g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0042g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0021g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0024g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0039g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0022g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0013t0025g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0013t0025g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0014t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0014t0038g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0022t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0024t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0030t0043g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0037t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0038t0044g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0017g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0018g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0019g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0019g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0026g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0027g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0028g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0029g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0030g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0032g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0047g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0011t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0011t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0011t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0017t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0019t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0020t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0029t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0032t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0035t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0036t0036g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0011g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0011g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0024g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0041g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0010t0014g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0010t0033g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0031t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0021t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0005c0008t0010g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0005c0008t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0005c0008t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0006c0016t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0006c0023t0011g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0007c0012t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0007c0012t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0008c0039t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0009c0015t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0010c0018t0022g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0011c0025t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0012c0028t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0013c0027t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0014c0026t0045g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0015c0033t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0016c0034t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0108 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0077 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0161 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0260 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0171 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00423 | hp2 | a0001 | c0007 | t0002 | g0205 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00558 | hp1 | a0002 | c0029 | t0001 | g0153 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00558 | hp2 | a0006 | c0016 | t0001 | g0124 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00597 | hp1 | a0001 | c0003 | t0004 | g0037 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0141 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00609 | hp1 | a0003 | c0010 | t0033 | g0146 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00609 | hp2 | a0002 | c0011 | t0002 | g0231 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00673 | hp2 | a0004 | c0021 | t0014 | g0222 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0137 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01069 | hp1 | a0001 | c0002 | t0012 | g0002 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01069 | hp2 | a0009 | c0015 | t0001 | g0085 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0165 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01071 | hp2 | a0001 | c0002 | t0012 | g0002 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0145 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01074 | hp2 | a0001 | c0002 | t0021 | g0233 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01081 | hp1 | a0001 | c0002 | t0023 | g0212 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01081 | hp2 | a0001 | c0014 | t0038 | g0152 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01099 | hp1 | a0001 | c0003 | t0004 | g0042 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01106 | hp2 | a0002 | c0001 | t0003 | g0071 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01109 | hp2 | a0001 | c0002 | t0034 | g0187 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01167 | hp1 | a0001 | c0003 | t0004 | g0047 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01175 | hp1 | a0001 | c0004 | t0006 | g0240 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0086 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0010 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0043 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01243 | hp1 | a0001 | c0002 | t0015 | g0016 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0191 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0056 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01255 | hp2 | a0001 | c0003 | t0004 | g0041 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01358 | hp2 | a0001 | c0002 | t0046 | g0234 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01361 | hp1 | a0001 | c0009 | t0002 | g0248 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0156 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0135 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01516 | hp1 | a0002 | c0001 | t0017 | g0004 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0118 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01517 | hp1 | a0002 | c0017 | t0004 | g0039 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01517 | hp2 | a0002 | c0001 | t0017 | g0004 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0197 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01884 | hp2 | a0003 | c0005 | t0006 | g0211 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0162 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0149 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01952 | hp1 | a0011 | c0025 | t0003 | g0186 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01952 | hp2 | a0002 | c0001 | t0003 | g0127 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0073 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0238 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0070 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02015 | hp1 | a0003 | c0005 | t0002 | g0014 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02015 | hp2 | a0001 | c0038 | t0044 | g0210 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02027 | hp1 | a0001 | c0003 | t0004 | g0030 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02040 | hp1 | a0002 | c0001 | t0032 | g0129 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0148 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02055 | hp1 | a0001 | c0009 | t0002 | g0249 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0133 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02056 | hp1 | a0001 | c0003 | t0004 | g0032 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02056 | hp2 | a0003 | c0010 | t0014 | g0013 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02071 | hp1 | a0002 | c0001 | t0019 | g0075 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02071 | hp2 | a0010 | c0018 | t0022 | g0209 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02129 | hp1 | a0006 | c0023 | t0011 | g0229 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02135 | hp1 | a0003 | c0005 | t0002 | g0014 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02145 | hp1 | a0005 | c0008 | t0010 | g0180 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02145 | hp2 | a0001 | c0003 | t0005 | g0057 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0239 | EAS | CDX | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | CDX | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02257 | hp1 | a0001 | c0002 | t0008 | g0062 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02257 | hp2 | a0002 | c0019 | t0009 | g0101 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02258 | hp1 | a0002 | c0001 | t0030 | g0053 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02258 | hp2 | a0001 | c0003 | t0012 | g0003 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02300 | hp1 | a0001 | c0009 | t0002 | g0247 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0170 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02451 | hp1 | a0001 | c0002 | t0040 | g0202 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02451 | hp2 | a0001 | c0003 | t0020 | g0182 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02523 | hp1 | a0004 | c0006 | t0001 | g0188 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02523 | hp2 | a0015 | c0033 | t0005 | g0094 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02572 | hp1 | a0001 | c0030 | t0043 | g0213 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02572 | hp2 | a0005 | c0008 | t0010 | g0179 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02615 | hp1 | a0001 | c0003 | t0008 | g0058 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02615 | hp2 | a0001 | c0002 | t0023 | g0256 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0201 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0215 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02630 | hp1 | a0002 | c0001 | t0009 | g0100 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02630 | hp2 | a0001 | c0003 | t0013 | g0049 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02647 | hp1 | a0003 | c0005 | t0005 | g0074 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02647 | hp2 | a0001 | c0003 | t0020 | g0178 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0167 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02683 | hp2 | a0001 | c0022 | t0002 | g0264 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0021 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02717 | hp2 | a0002 | c0036 | t0036 | g0109 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02723 | hp1 | a0001 | c0024 | t0006 | g0200 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02723 | hp2 | a0001 | c0002 | t0037 | g0177 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0136 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02735 | hp2 | a0001 | c0009 | t0002 | g0246 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0259 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02809 | hp1 | a0001 | c0002 | t0010 | g0181 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02809 | hp2 | a0002 | c0001 | t0028 | g0120 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02818 | hp1 | a0001 | c0013 | t0025 | g0266 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02818 | hp2 | a0014 | c0026 | t0045 | g0204 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02895 | hp1 | a0001 | c0003 | t0013 | g0050 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02895 | hp2 | a0005 | c0008 | t0010 | g0011 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02897 | hp1 | a0002 | c0001 | t0009 | g0083 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02897 | hp2 | a0005 | c0008 | t0010 | g0011 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02922 | hp1 | a0001 | c0002 | t0007 | g0012 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02922 | hp2 | a0003 | c0005 | t0041 | g0257 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02965 | hp1 | a0002 | c0001 | t0005 | g0065 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02965 | hp2 | a0001 | c0003 | t0035 | g0183 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02970 | hp1 | a0002 | c0001 | t0027 | g0098 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02970 | hp2 | a0003 | c0005 | t0003 | g0007 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02976 | hp1 | a0001 | c0003 | t0008 | g0048 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02976 | hp2 | a0003 | c0005 | t0006 | g0230 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0119 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03041 | hp1 | a0002 | c0001 | t0018 | g0084 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03041 | hp2 | a0001 | c0013 | t0025 | g0267 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03098 | hp1 | a0001 | c0002 | t0011 | g0198 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03098 | hp2 | a0001 | c0002 | t0007 | g0193 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03130 | hp1 | a0001 | c0002 | t0015 | g0016 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03130 | hp2 | a0003 | c0005 | t0005 | g0122 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03139 | hp1 | a0001 | c0003 | t0013 | g0024 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03139 | hp2 | a0002 | c0001 | t0047 | g0265 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03195 | hp1 | a0003 | c0005 | t0003 | g0078 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0060 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03225 | hp1 | a0002 | c0001 | t0009 | g0130 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0121 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0164 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0242 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03453 | hp1 | a0001 | c0003 | t0008 | g0055 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0216 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03486 | hp1 | a0001 | c0002 | t0016 | g0017 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03486 | hp2 | a0001 | c0002 | t0048 | g0268 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0076 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0175 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0079 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03516 | hp1 | a0001 | c0002 | t0007 | g0012 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03516 | hp2 | a0003 | c0005 | t0003 | g0007 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03540 | hp1 | a0002 | c0001 | t0005 | g0099 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03540 | hp2 | a0001 | c0002 | t0015 | g0262 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0067 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0194 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03704 | hp1 | a0002 | c0011 | t0002 | g0263 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03704 | hp2 | a0001 | c0003 | t0004 | g0044 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03710 | hp1 | a0003 | c0005 | t0001 | g0166 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03710 | hp2 | a0002 | c0001 | t0003 | g0154 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0125 | SAS | BEB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04184 | hp2 | a0004 | c0006 | t0005 | g0123 | SAS | BEB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04199 | hp1 | a0001 | c0007 | t0022 | g0208 | SAS | STU | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04199 | hp2 | a0013 | c0027 | t0001 | g0169 | SAS | STU | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0103 | EAS | CHB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18747 | hp2 | a0003 | c0031 | t0003 | g0185 | EAS | CHB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18906 | hp1 | a0002 | c0035 | t0001 | g0173 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0061 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18939 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18940 | hp2 | a0001 | c0004 | t0006 | g0250 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18943 | hp1 | a0002 | c0011 | t0002 | g0241 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18944 | hp1 | a0001 | c0003 | t0004 | g0035 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18946 | hp1 | a0001 | c0004 | t0039 | g0235 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18949 | hp2 | a0004 | c0006 | t0001 | g0184 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18952 | hp1 | a0003 | c0005 | t0002 | g0219 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18954 | hp2 | a0002 | c0001 | t0004 | g0114 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18956 | hp1 | a0001 | c0003 | t0004 | g0027 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18956 | hp2 | a0008 | c0039 | t0001 | g0190 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18957 | hp2 | a0003 | c0005 | t0011 | g0218 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18962 | hp1 | a0001 | c0004 | t0024 | g0251 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18962 | hp2 | a0001 | c0003 | t0004 | g0031 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18965 | hp1 | a0001 | c0007 | t0002 | g0206 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18965 | hp2 | a0012 | c0028 | t0002 | g0214 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18967 | hp1 | a0001 | c0003 | t0042 | g0254 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18968 | hp2 | a0003 | c0005 | t0002 | g0228 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18969 | hp2 | a0001 | c0004 | t0006 | g0253 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18970 | hp2 | a0007 | c0012 | t0003 | g0019 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0159 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18971 | hp2 | a0001 | c0004 | t0021 | g0258 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18973 | hp2 | a0002 | c0032 | t0001 | g0095 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18975 | hp2 | a0003 | c0010 | t0014 | g0013 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18977 | hp1 | a0003 | c0005 | t0011 | g0223 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18977 | hp2 | a0002 | c0001 | t0019 | g0115 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18979 | hp1 | a0003 | c0005 | t0011 | g0227 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18986 | hp1 | a0004 | c0006 | t0002 | g0226 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18986 | hp2 | a0001 | c0003 | t0005 | g0038 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18988 | hp1 | a0007 | c0012 | t0003 | g0020 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18988 | hp2 | a0002 | c0001 | t0029 | g0110 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18991 | hp2 | a0001 | c0004 | t0002 | g0245 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18994 | hp1 | a0004 | c0006 | t0002 | g0221 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0236 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18999 | hp2 | a0001 | c0004 | t0002 | g0261 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19000 | hp2 | a0001 | c0003 | t0004 | g0033 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19005 | hp2 | a0003 | c0005 | t0002 | g0220 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19007 | hp2 | a0001 | c0004 | t0002 | g0244 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0097 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0203 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19030 | hp2 | a0003 | c0005 | t0003 | g0151 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19043 | hp1 | a0002 | c0001 | t0018 | g0102 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19043 | hp2 | a0001 | c0003 | t0005 | g0059 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19056 | hp1 | a0002 | c0001 | t0004 | g0081 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19056 | hp2 | a0001 | c0003 | t0004 | g0046 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19062 | hp1 | a0002 | c0001 | t0026 | g0163 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19064 | hp1 | a0004 | c0006 | t0002 | g0225 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19064 | hp2 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19066 | hp1 | a0001 | c0007 | t0002 | g0207 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19066 | hp2 | a0002 | c0020 | t0001 | g0069 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19068 | hp1 | a0001 | c0004 | t0002 | g0252 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19079 | hp1 | a0001 | c0004 | t0002 | g0237 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19083 | hp1 | a0003 | c0005 | t0024 | g0224 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19086 | hp2 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19090 | hp1 | a0001 | c0003 | t0004 | g0036 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19240 | hp1 | a0001 | c0002 | t0007 | g0195 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0052 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20129 | hp1 | a0001 | c0002 | t0007 | g0192 | AFR | ASW | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0199 | AFR | ASW | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0176 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20752 | hp2 | a0001 | c0003 | t0004 | g0029 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20805 | hp1 | a0001 | c0037 | t0002 | g0232 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20805 | hp2 | a0001 | c0003 | t0031 | g0063 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | GIH | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20905 | hp2 | a0003 | c0005 | t0002 | g0217 | SAS | GIH | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02109 | hp1 | a0001 | c0002 | t0008 | g0051 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02109 | hp2 | a0001 | c0003 | t0012 | g0003 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0034 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0066 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03471 | hp1 | a0002 | c0001 | t0009 | g0131 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03471 | hp2 | a0001 | c0002 | t0016 | g0018 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG06807 | hp1 | a0002 | c0001 | t0001 | g0064 | AFR | USA | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG06807 | hp2 | a0001 | c0014 | t0003 | g0168 | AFR | USA | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18955 | hp1 | a0001 | c0003 | t0004 | g0045 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA21309 | hp1 | a0001 | c0003 | t0013 | g0054 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA21309 | hp2 | a0016 | c0034 | t0003 | g0134 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0138 | REF | REF | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0155 | REF | REF | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95446931
|
C | T | 1 | a0012 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.4325G>A | p.Arg1442Gln | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 5230/8662 | 4325/4344 | 1442/1447 | chr9 | 95446931 | ||
| chr9:95446967
|
A | G | 1 | a0014 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.4289T>C | p.Ile1430Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 5194/8662 | 4289/4344 | 1430/1447 | chr9 | 95446967 | ||
| chr9:95447108
|
G | A | 1 | a0013 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.4148C>T | p.Pro1383Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 5053/8662 | 4148/4344 | 1383/1447 | chr9 | 95447108 | ||
| chr9:95447312
|
G | A | 7 | a0002a0004a0008others(4): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
missense_variant | MODERATE | c.3944C>T | p.Pro1315Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4849/8662 | 3944/4344 | 1315/1447 | chr9 | 95447312 | ||
| chr9:95447349
|
G | A | 1 | a0006 | 2 | HG00558.hp2 HG02129.hp1 |
missense_variant | MODERATE | c.3907C>T | p.Arg1303Cys | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4812/8662 | 3907/4344 | 1303/1447 | chr9 | 95447349 | ||
| chr9:95447411
|
G | A | 1 | a0005 | 4 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.3845C>T | p.Pro1282Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4750/8662 | 3845/4344 | 1282/1447 | chr9 | 95447411 | ||
| chr9:95449107
|
C | T | 1 | a0011 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.3766G>A | p.Val1256Met | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4671/8662 | 3766/4344 | 1256/1447 | chr9 | 95449107 | ||
| chr9:95449290
|
T | A | 4 | a0003a0004a0006others(1): Show | 35 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
missense_variant | MODERATE | c.3583A>T | p.Thr1195Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4488/8662 | 3583/4344 | 1195/1447 | chr9 | 95449290 | ||
| chr9:95467197
|
T | C | 1 | a0010 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2479A>G | p.Ser827Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/24 | 3384/8662 | 2479/4344 | 827/1447 | chr9 | 95467197 | ||
| chr9:95468779
|
G | A | 1 | a0015 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2222C>T | p.Ala741Val | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 3127/8662 | 2222/4344 | 741/1447 | chr9 | 95468779 | ||
| chr9:95468828
|
G | A | 1 | a0016 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2173C>T | p.Pro725Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 3078/8662 | 2173/4344 | 725/1447 | chr9 | 95468828 | ||
| chr9:95476101
|
C | T | 1 | a0009 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1661G>A | p.Ser554Asn | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/24 | 2566/8662 | 1661/4344 | 554/1447 | chr9 | 95476101 | ||
| chr9:95508253
|
C | G | 1 | a0007 | 2 | NA18970.hp2 NA18988.hp1 |
missense_variant | MODERATE | c.109G>C | p.Gly37Arg | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 1014/8662 | 109/4344 | 37/1447 | chr9 | 95508253 | ||
| chr9:95508325
|
G | C | 1 | a0008 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.37C>G | p.Arg13Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 942/8662 | 37/4344 | 13/1447 | chr9 | 95508325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95447176
|
G | A | 2 | a0001c0037a0002c0029 | 2 | HG00558.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.4080C>T | p.Ser1360Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4985/8662 | 4080/4344 | 1360/1447 | chr9 | 95447176 | ||
| chr9:95449186
|
C | T | 1 | a0001c0024 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3687G>A | p.Thr1229Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4592/8662 | 3687/4344 | 1229/1447 | chr9 | 95449186 | ||
| chr9:95449249
|
G | A | 1 | a0001c0030 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3624C>T | p.Ala1208Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4529/8662 | 3624/4344 | 1208/1447 | chr9 | 95449249 | ||
| chr9:95449306
|
G | A | 1 | a0001c0014 | 2 | HG01081.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3567C>T | p.Gly1189Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4472/8662 | 3567/4344 | 1189/1447 | chr9 | 95449306 | ||
| chr9:95453540
|
G | A | 1 | a0002c0032 | 1 | NA18973.hp2 | synonymous_variant | LOW | c.3387C>T | p.Gly1129Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/24 | 4292/8662 | 3387/4344 | 1129/1447 | chr9 | 95453540 | ||
| chr9:95456387
|
G | A | 1 | a0002c0036 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.3195C>T | p.Val1065Val | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/24 | 4100/8662 | 3195/4344 | 1065/1447 | chr9 | 95456387 | ||
| chr9:95458040
|
A | C | 7 | a0001c0022a0003c0005a0003c0010others(4): Show | 33 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
synonymous_variant | LOW | c.3141T>G | p.Leu1047Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/24 | 4046/8662 | 3141/4344 | 1047/1447 | chr9 | 95458040 | ||
| chr9:95458268
|
A | G | 2 | a0003c0010a0004c0021 | 4 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(1): Show |
synonymous_variant | LOW | c.2913T>C | p.Tyr971Tyr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/24 | 3818/8662 | 2913/4344 | 971/1447 | chr9 | 95458268 | ||
| chr9:95458271
|
C | T | 1 | a0002c0020 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2910G>A | p.Glu970Glu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/24 | 3815/8662 | 2910/4344 | 970/1447 | chr9 | 95458271 | ||
| chr9:95459688
|
C | T | 1 | a0001c0013 | 2 | HG02818.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.2799G>A | p.Ala933Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/24 | 3704/8662 | 2799/4344 | 933/1447 | chr9 | 95459688 | ||
| chr9:95468802
|
T | C | 3 | a0001c0007a0001c0038a0010c0018 | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
synonymous_variant | LOW | c.2199A>G | p.Ser733Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 3104/8662 | 2199/4344 | 733/1447 | chr9 | 95468802 | ||
| chr9:95469039
|
C | T | 1 | a0002c0019 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1962G>A | p.Thr654Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 2867/8662 | 1962/4344 | 654/1447 | chr9 | 95469039 | ||
| chr9:95469147
|
G | A | 2 | a0002c0035a0002c0036 | 2 | HG02717.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1854C>T | p.Cys618Cys | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 2759/8662 | 1854/4344 | 618/1447 | chr9 | 95469147 | ||
| chr9:95476076
|
G | A | 4 | a0001c0004a0001c0009a0001c0037others(1): Show | 33 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(30): Show |
synonymous_variant | LOW | c.1686C>T | p.Ala562Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/24 | 2591/8662 | 1686/4344 | 562/1447 | chr9 | 95476076 | ||
| chr9:95476097
|
A | G | 6 | a0001c0003a0001c0007a0001c0038others(3): Show | 53 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
synonymous_variant | LOW | c.1665T>C | p.Asn555Asn | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/24 | 2570/8662 | 1665/4344 | 555/1447 | chr9 | 95476097 | ||
| chr9:95481960
|
T | C | 1 | a0001c0009 | 4 | HG01361.hp1 HG02055.hp1 HG02300.hp1 others(1): Show |
synonymous_variant | LOW | c.735A>G | p.Thr245Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/24 | 1640/8662 | 735/4344 | 245/1447 | chr9 | 95481960 | ||
| chr9:95506597
|
C | A | 1 | a0001c0038 | 1 | HG02015.hp2 | splice_region_variant&synonymous_variant | LOW | c.204G>T | p.Gly68Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/24 | 1109/8662 | 204/4344 | 68/1447 | chr9 | 95506597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95443161
|
C | A | 17 | a0001c0002t0003a0001c0002t0006a0001c0002t0040others(14): Show | 43 | HG00099.hp1 HG01071.hp1 HG01074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3232G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3751 | chr9 | 95443161 | |||||
| chr9:95443236
|
C | T | 3 | a0001c0007t0022a0001c0038t0044a0010c0018t0022 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3157G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3676 | chr9 | 95443236 | |||||
| chr9:95443363
|
T | C | 36 | a0001c0002t0005a0001c0002t0007a0001c0002t0008others(33): Show | 81 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*3030A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3549 | chr9 | 95443363 | |||||
| chr9:95443397
|
TACAA | T | 2 | a0001c0002t0012a0001c0003t0012 | 4 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2992_*2995delTTGT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3511 | chr9 | 95443397 | |||||
| chr9:95443613
|
T | A | 1 | a0002c0001t0032 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2780A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3299 | chr9 | 95443613 | |||||
| chr9:95443735
|
A | C | 1 | a0002c0036t0036 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3177 | chr9 | 95443735 | |||||
| chr9:95444104
|
G | GT | 12 | a0001c0002t0005a0001c0002t0011a0001c0003t0005others(9): Show | 21 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2288dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2807 | chr9 | 95444104 | |||||
| chr9:95444117
|
T | A | 1 | a0001c0013t0025 | 2 | HG02818.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2795 | chr9 | 95444117 | |||||
| chr9:95444117
|
TA | T | 3 | a0001c0007t0022a0002c0001t0018a0010c0018t0022 | 4 | HG02071.hp2 HG03041.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2275delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2794 | chr9 | 95444117 | |||||
| chr9:95444118
|
A | T | 17 | a0001c0002t0007a0001c0002t0012a0001c0002t0015others(14): Show | 33 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2275T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2794 | chr9 | 95444118 | |||||
| chr9:95444488
|
G | C | 9 | a0001c0002t0007a0001c0002t0037a0002c0001t0009others(6): Show | 19 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1905C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2424 | chr9 | 95444488 | |||||
| chr9:95444491
|
ACACACAC others(11): Show |
A | 3 | a0001c0007t0022a0001c0038t0044a0010c0018t0022 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1884_*1901delCGTG others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2403 | chr9 | 95444491 | |||||
| chr9:95444509
|
G | GCA | 22 | a0001c0002t0005a0001c0002t0008a0001c0002t0011others(19): Show | 55 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1883dupTG | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | |||||
| chr9:95444509
|
G | GCACACA | 7 | a0001c0002t0007a0001c0002t0037a0002c0001t0009others(4): Show | 17 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1878_*1883dupTGTG others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | |||||
| chr9:95444509
|
G | GCACACAC others(3): Show |
1 | a0002c0001t0028 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1874_*1883dupTGTG others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | |||||
| chr9:95444571
|
T | G | 1 | a0001c0003t0042 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1822A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2341 | chr9 | 95444571 | |||||
| chr9:95444684
|
C | T | 9 | a0001c0002t0007a0001c0002t0037a0002c0001t0009others(6): Show | 19 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1709G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2228 | chr9 | 95444684 | |||||
| chr9:95444685
|
G | A | 4 | a0002c0001t0019a0003c0010t0014a0003c0010t0033others(1): Show | 6 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1708C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2227 | chr9 | 95444685 | |||||
| chr9:95444691
|
G | A | 6 | a0002c0001t0009a0002c0001t0018a0002c0001t0027others(3): Show | 10 | HG02257.hp2 HG02630.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1702C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2221 | chr9 | 95444691 | |||||
| chr9:95444777
|
T | G | 9 | a0001c0002t0007a0001c0002t0037a0002c0001t0009others(6): Show | 19 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1616A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2135 | chr9 | 95444777 | |||||
| chr9:95444848
|
A | G | 3 | a0001c0002t0016a0001c0003t0020a0001c0014t0038 | 5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1545T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2064 | chr9 | 95444848 | |||||
| chr9:95444858
|
A | G | 3 | a0001c0002t0016a0001c0003t0020a0001c0014t0038 | 5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2054 | chr9 | 95444858 | |||||
| chr9:95445020
|
C | G | 7 | a0001c0002t0021a0001c0003t0004a0001c0003t0042others(4): Show | 27 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1373G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1892 | chr9 | 95445020 | |||||
| chr9:95445039
|
A | C | 1 | a0002c0001t0030 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1873 | chr9 | 95445039 | |||||
| chr9:95445327
|
T | G | 2 | a0001c0003t0020a0001c0014t0038 | 3 | HG01081.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1066A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1585 | chr9 | 95445327 | |||||
| chr9:95445542
|
C | G | 1 | a0001c0002t0007 | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*851G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1370 | chr9 | 95445542 | |||||
| chr9:95445592
|
G | A | 1 | a0001c0014t0038 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1320 | chr9 | 95445592 | |||||
| chr9:95445606
|
G | A | 2 | a0001c0004t0024a0003c0005t0024 | 2 | NA18962.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1306 | chr9 | 95445606 | |||||
| chr9:95445613
|
G | A | 3 | a0001c0007t0022a0001c0038t0044a0010c0018t0022 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1299 | chr9 | 95445613 | |||||
| chr9:95445644
|
G | GAAAT | 3 | a0001c0007t0022a0001c0038t0044a0010c0018t0022 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*748_*749insATTT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1267 | chr9 | 95445644 | |||||
| chr9:95445644
|
G | GAAGT | 8 | a0001c0002t0021a0001c0003t0004a0001c0003t0042others(5): Show | 28 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*748_*749insACTT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1267 | chr9 | 95445644 | |||||
| chr9:95445728
|
C | CA | 23 | a0001c0002t0007a0001c0002t0010a0001c0002t0012others(20): Show | 46 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*664dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1183 | chr9 | 95445728 | |||||
| chr9:95445943
|
T | G | 1 | a0001c0002t0046 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 969 | chr9 | 95445943 | |||||
| chr9:95446156
|
C | G | 12 | a0001c0002t0007a0001c0002t0012a0001c0002t0040others(9): Show | 27 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 756 | chr9 | 95446156 | |||||
| chr9:95446162
|
A | G | 1 | a0002c0001t0017 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 750 | chr9 | 95446162 | |||||
| chr9:95446248
|
A | G | 1 | a0002c0001t0026 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 664 | chr9 | 95446248 | |||||
| chr9:95446288
|
C | T | 1 | a0001c0004t0039 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 624 | chr9 | 95446288 | |||||
| chr9:95446308
|
C | T | 2 | a0001c0002t0012a0001c0003t0012 | 4 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 604 | chr9 | 95446308 | |||||
| chr9:95508364
|
T | TGCC | 40 | a0001c0002t0002a0001c0002t0006a0001c0002t0007others(37): Show | 88 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
5_prime_UTR_variant | MODIFIER | c.-6_-4dupGGC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 4 | chr9 | 95508364 | |||||
| chr9:95508628
|
G | A | 1 | a0002c0001t0047 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 267 | chr9 | 95508628 | |||||
| chr9:95508702
|
T | G | 2 | a0001c0002t0048a0001c0013t0025 | 3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-341A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 341 | chr9 | 95508702 | |||||
| chr9:95509256
|
G | T | 1 | a0001c0002t0016 | 2 | HG03471.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-895C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 895 | chr9 | 95509256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95446437
|
G | A | 1 | a0001c0002t0034g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*2-46C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446437 | ||||||
| chr9:95446505
|
G | A | 5 | a0001c0002t0001g0128a0001c0002t0001g0150a0001c0004t0024g0251others(2): Show | 5 | NA18962.hp1 NA19004.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.*2-114C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446505 | ||||||
| chr9:95446508
|
G | A | 1 | a0002c0001t0004g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.*2-117C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446508 | ||||||
| chr9:95446571
|
C | T | 1 | a0001c0009t0002g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*2-180G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446571 | ||||||
| chr9:95446682
|
C | T | 2 | a0001c0002t0021g0233a0001c0003t0004g0034 | 2 | HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.*1+229G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446682 | ||||||
| chr9:95446773
|
A | G | 2 | a0001c0002t0007g0195a0002c0036t0036g0109 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*1+138T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446773 | ||||||
| chr9:95446812
|
C | T | 1 | a0002c0001t0001g0089 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.*1+99G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446812 | ||||||
| chr9:95446874
|
T | C | 20 | a0001c0004t0002g0245a0002c0001t0001g0006a0002c0001t0001g0082others(17): Show | 21 | HG00597.hp2 HG02040.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.*1+37A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446874 | ||||||
| chr9:95446904
|
C | T | 1 | a0002c0001t0001g0113 | 1 | NA18975.hp1 | splice_region_variant&intron_variant | LOW | c.*1+7G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446904 | ||||||
| chr9:95447460
|
G | A | 1 | a0012c0028t0002g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3805-9C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447460 | ||||||
| chr9:95447617
|
C | T | 8 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(5): Show | 9 | HG00423.hp2 HG00609.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.3805-166G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447617 | ||||||
| chr9:95447648
|
A | T | 9 | a0001c0002t0003g0021a0001c0002t0003g0121a0001c0002t0006g0199others(6): Show | 11 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3805-197T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447648 | ||||||
| chr9:95447676
|
G | A | 28 | a0001c0002t0003g0021a0001c0002t0003g0121a0001c0002t0006g0199others(25): Show | 33 | HG00423.hp2 HG00609.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.3805-225C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447676 | ||||||
| chr9:95447802
|
G | A | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3805-351C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447802 | ||||||
| chr9:95447888
|
G | A | 8 | a0001c0002t0005g0066a0003c0005t0005g0122a0003c0005t0006g0211others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3805-437C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447888 | ||||||
| chr9:95448223
|
C | T | 2 | a0001c0002t0008g0051a0001c0002t0008g0052 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3805-772G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448223 | ||||||
| chr9:95448224
|
G | A | 1 | a0001c0002t0007g0195 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3805-773C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448224 | ||||||
| chr9:95448227
|
C | T | 1 | a0001c0002t0006g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3805-776G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448227 | ||||||
| chr9:95448659
|
G | T | 59 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(56): Show | 60 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.3804+410C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448659 | ||||||
| chr9:95448730
|
G | GA | 33 | a0001c0003t0004g0030a0003c0005t0001g0166a0003c0005t0002g0014others(30): Show | 36 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.3804+338dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448730 | ||||||
| chr9:95449438
|
C | A | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3550-115G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449438 | ||||||
| chr9:95449661
|
G | A | 1 | a0001c0003t0001g0001 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3549+180C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449661 | ||||||
| chr9:95449678
|
C | G | 1 | a0001c0009t0002g0246 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3549+163G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449678 | ||||||
| chr9:95449706
|
C | T | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3549+135G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449706 | ||||||
| chr9:95449803
|
C | A | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3549+38G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449803 | ||||||
| chr9:95450027
|
C | T | 1 | a0001c0003t0004g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3450-87G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450027 | ||||||
| chr9:95450072
|
A | C | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3450-132T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450072 | ||||||
| chr9:95450238
|
A | G | 1 | a0002c0035t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3450-298T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450238 | ||||||
| chr9:95450270
|
C | T | 8 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(5): Show | 8 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3450-330G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450270 | ||||||
| chr9:95450326
|
C | T | 29 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(26): Show | 30 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3450-386G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450326 | ||||||
| chr9:95450788
|
G | C | 3 | a0001c0003t0005g0057a0001c0003t0008g0058a0011c0025t0003g0186 | 3 | HG01952.hp1 HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3450-848C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450788 | ||||||
| chr9:95451004
|
A | AG | 32 | a0001c0002t0034g0187a0001c0002t0046g0234a0001c0004t0001g0076others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.3450-1065dupC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451004 | ||||||
| chr9:95451071
|
T | G | 2 | a0001c0014t0003g0168a0001c0014t0038g0152 | 2 | HG01081.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3450-1131A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451071 | ||||||
| chr9:95451404
|
G | C | 1 | a0001c0003t0013g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3450-1464C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451404 | ||||||
| chr9:95451446
|
C | G | 31 | a0001c0002t0046g0234a0001c0004t0001g0076a0001c0004t0001g0077others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.3450-1506G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451446 | ||||||
| chr9:95451478
|
G | A | 1 | a0001c0004t0001g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3450-1538C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451478 | ||||||
| chr9:95451627
|
T | C | 2 | a0001c0002t0008g0051a0001c0002t0008g0052 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3450-1687A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451627 | ||||||
| chr9:95452085
|
A | G | 31 | a0001c0002t0046g0234a0001c0004t0001g0076a0001c0004t0001g0077others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.3449+1393T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452085 | ||||||
| chr9:95452328
|
G | GAC | 6 | a0001c0002t0001g0080a0001c0002t0001g0087a0001c0002t0003g0056others(3): Show | 6 | HG01255.hp1 HG02451.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3449+1148_3449+114 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACAC | 12 | a0001c0002t0002g0196a0001c0002t0006g0203a0001c0002t0007g0012others(9): Show | 15 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.3449+1144_3449+114 others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(1): Show |
8 | a0001c0002t0002g0197a0001c0002t0003g0021a0001c0002t0003g0121others(5): Show | 8 | HG01358.hp2 HG01884.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3449+1142_3449+114 others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(3): Show |
34 | a0001c0002t0008g0062a0001c0002t0016g0017a0001c0002t0016g0018others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.3449+1140_3449+114 others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(5): Show |
12 | a0001c0003t0004g0035a0001c0003t0004g0043a0001c0003t0005g0057others(9): Show | 12 | HG00423.hp2 HG01192.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.3449+1138_3449+114 others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(7): Show |
10 | a0001c0002t0008g0051a0001c0002t0008g0052a0001c0002t0011g0198others(7): Show | 10 | HG02027.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3449+1136_3449+114 others(18): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(9): Show |
25 | a0001c0002t0037g0177a0001c0003t0001g0001a0001c0003t0001g0028others(22): Show | 26 | HG00738.hp2 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.3449+1134_3449+114 others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(11): Show |
5 | a0001c0003t0004g0036a0001c0004t0021g0258a0001c0007t0022g0208others(2): Show | 5 | HG01517.hp1 HG02015.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.3449+1132_3449+114 others(22): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(13): Show |
1 | a0001c0003t0005g0038 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3449+1130_3449+114 others(24): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(15): Show |
1 | a0001c0003t0004g0037 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3449+1128_3449+114 others(26): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
GAC | G | 89 | a0001c0002t0001g0072a0001c0002t0002g0255a0001c0002t0010g0181others(86): Show | 98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3449+1148_3449+114 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452356
|
C | CACACACA others(6): Show |
1 | a0001c0002t0021g0233 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3449+1121_3449+112 others(17): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452356 | ||||||
| chr9:95452357
|
A | ACACACAC others(12): Show |
1 | a0001c0003t0042g0254 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3449+1120_3449+112 others(23): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452357 | ||||||
| chr9:95452376
|
G | A | 1 | a0001c0002t0003g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3449+1102C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452376 | ||||||
| chr9:95452476
|
C | T | 42 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(39): Show | 45 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.3449+1002G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452476 | ||||||
| chr9:95452903
|
T | C | 29 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(26): Show | 30 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3449+575A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452903 | ||||||
| chr9:95453024
|
C | T | 54 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(51): Show | 59 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.3449+454G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453024 | ||||||
| chr9:95453046
|
T | C | 6 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3449+432A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453046 | ||||||
| chr9:95453113
|
C | A | 1 | a0003c0005t0003g0151 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3449+365G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453113 | ||||||
| chr9:95453114
|
G | A | 1 | a0001c0003t0004g0026 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3449+364C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453114 | ||||||
| chr9:95453141
|
T | A | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3449+337A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453141 | ||||||
| chr9:95453244
|
G | A | 1 | a0001c0009t0002g0248 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3449+234C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453244 | ||||||
| chr9:95453349
|
T | C | 40 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.3449+129A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453349 | ||||||
| chr9:95453686
|
C | G | 32 | a0003c0005t0001g0166a0003c0005t0002g0014a0003c0005t0002g0217others(29): Show | 35 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.3307-66G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453686 | ||||||
| chr9:95453772
|
C | A | 1 | a0002c0001t0001g0158 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3307-152G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453772 | ||||||
| chr9:95453772
|
C | T | 6 | a0001c0002t0008g0051a0001c0002t0008g0052a0001c0002t0008g0062others(3): Show | 6 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3307-152G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453772 | ||||||
| chr9:95453991
|
T | C | 6 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3307-371A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453991 | ||||||
| chr9:95454363
|
A | G | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3307-743T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95454363 | ||||||
| chr9:95454594
|
A | G | 156 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(153): Show | 166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.3307-974T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95454594 | ||||||
| chr9:95454804
|
C | G | 1 | a0001c0002t0048g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3307-1184G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95454804 | ||||||
| chr9:95455066
|
A | G | 97 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(94): Show | 102 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.3306+1210T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455066 | ||||||
| chr9:95455226
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0087a0002c0001t0001g0119 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3306+1050G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455226 | ||||||
| chr9:95455299
|
T | C | 156 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(153): Show | 166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.3306+977A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455299 | ||||||
| chr9:95455328
|
G | A | 3 | a0001c0002t0001g0144a0001c0002t0003g0145a0001c0002t0003g0165 | 3 | HG01071.hp1 HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3306+948C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455328 | ||||||
| chr9:95455442
|
C | G | 9 | a0001c0003t0005g0059a0001c0003t0005g0060a0001c0003t0005g0061others(6): Show | 9 | HG02630.hp2 HG02895.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.3306+834G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455442 | ||||||
| chr9:95455462
|
C | T | 2 | a0001c0002t0002g0196a0001c0002t0002g0197 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3306+814G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455462 | ||||||
| chr9:95455495
|
T | C | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3306+781A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455495 | ||||||
| chr9:95455507
|
A | G | 3 | a0001c0003t0020g0178a0001c0014t0003g0168a0001c0014t0038g0152 | 3 | HG01081.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3306+769T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455507 | ||||||
| chr9:95455728
|
T | G | 2 | a0001c0002t0012g0002a0001c0003t0012g0003 | 4 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3306+548A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455728 | ||||||
| chr9:95455759
|
C | T | 8 | a0001c0002t0008g0051a0001c0002t0008g0052a0001c0002t0008g0062others(5): Show | 8 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3306+517G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455759 | ||||||
| chr9:95455760
|
G | A | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3306+516C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455760 | ||||||
| chr9:95455960
|
G | A | 2 | a0002c0035t0001g0173a0002c0036t0036g0109 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3306+316C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455960 | ||||||
| chr9:95456030
|
C | T | 1 | a0003c0005t0002g0228 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3306+246G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95456030 | ||||||
| chr9:95456160
|
G | A | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3306+116C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95456160 | ||||||
| chr9:95456192
|
G | GC | 157 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(154): Show | 167 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.3306+83dupG | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95456192 | ||||||
| chr9:95456418
|
A | G | 2 | a0001c0002t0001g0080a0001c0002t0001g0087 | 2 | HG03491.hp2 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.3169-5T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456418 | ||||||
| chr9:95456710
|
G | A | 1 | a0003c0005t0006g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3169-297C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456710 | ||||||
| chr9:95456755
|
C | T | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3169-342G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456755 | ||||||
| chr9:95456761
|
T | TCA | 8 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(5): Show | 8 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.3169-350_3169-349d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456761 | ||||||
| chr9:95456984
|
G | A | 1 | a0002c0020t0001g0069 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3169-571C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456984 | ||||||
| chr9:95457009
|
C | T | 4 | a0001c0002t0003g0009a0001c0002t0003g0023a0001c0002t0003g0143others(1): Show | 5 | HG01358.hp1 HG01934.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.3169-596G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457009 | ||||||
| chr9:95457022
|
C | G | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3169-609G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457022 | ||||||
| chr9:95457565
|
T | C | 4 | a0002c0001t0001g0082a0002c0001t0001g0112a0002c0001t0001g0139others(1): Show | 4 | NA18939.hp1 NA18967.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.3168+448A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457565 | ||||||
| chr9:95457667
|
T | C | 1 | a0002c0001t0001g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3168+346A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457667 | ||||||
| chr9:95457755
|
G | A | 3 | a0002c0001t0001g0070a0002c0001t0001g0073a0002c0001t0017g0004 | 4 | HG01516.hp1 HG01517.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3168+258C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457755 | ||||||
| chr9:95457777
|
G | C | 1 | a0001c0002t0006g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3168+236C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457777 | ||||||
| chr9:95457780
|
C | T | 1 | a0003c0005t0006g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3168+233G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457780 | ||||||
| chr9:95457793
|
C | T | 1 | a0002c0001t0003g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3168+220G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457793 | ||||||
| chr9:95458432
|
T | C | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2888-139A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458432 | ||||||
| chr9:95458564
|
C | T | 2 | a0001c0002t0002g0196a0001c0002t0002g0197 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2888-271G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458564 | ||||||
| chr9:95458576
|
AT | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2888-284delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458576 | ||||||
| chr9:95458939
|
C | T | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2888-646G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458939 | ||||||
| chr9:95459017
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2887+583C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459017 | ||||||
| chr9:95459272
|
C | T | 3 | a0003c0010t0014g0013a0003c0010t0033g0146a0004c0021t0014g0222 | 4 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2887+328G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459272 | ||||||
| chr9:95459306
|
C | T | 1 | a0001c0003t0013g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2887+294G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459306 | ||||||
| chr9:95459340
|
G | A | 1 | a0001c0014t0038g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2887+260C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459340 | ||||||
| chr9:95459418
|
G | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2887+182C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459418 | ||||||
| chr9:95459512
|
G | A | 1 | a0002c0001t0001g0093 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2887+88C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459512 | ||||||
| chr9:95459563
|
T | C | 3 | a0001c0002t0015g0016a0001c0002t0015g0262a0001c0002t0034g0187 | 4 | HG01109.hp2 HG01243.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2887+37A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459563 | ||||||
| chr9:95459579
|
T | C | 156 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(153): Show | 166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.2887+21A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459579 | ||||||
| chr9:95459891
|
T | C | 2 | a0001c0002t0003g0136a0001c0002t0003g0175 | 2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2704-108A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95459891 | ||||||
| chr9:95460072
|
A | G | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2704-289T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460072 | ||||||
| chr9:95460145
|
C | T | 4 | a0002c0001t0001g0082a0002c0001t0001g0112a0002c0001t0001g0139others(1): Show | 4 | NA18939.hp1 NA18967.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.2704-362G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460145 | ||||||
| chr9:95460298
|
G | A | 4 | a0001c0002t0010g0181a0005c0008t0010g0011a0005c0008t0010g0179others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2704-515C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460298 | ||||||
| chr9:95460299
|
T | G | 1 | a0002c0001t0003g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2704-516A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460299 | ||||||
| chr9:95460349
|
G | A | 1 | a0011c0025t0003g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2704-566C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460349 | ||||||
| chr9:95460365
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2704-582G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460365 | ||||||
| chr9:95460369
|
C | T | 34 | a0001c0022t0002g0264a0003c0005t0001g0166a0003c0005t0002g0014others(31): Show | 37 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.2704-586G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460369 | ||||||
| chr9:95460371
|
C | T | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2704-588G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460371 | ||||||
| chr9:95460383
|
C | T | 41 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(38): Show | 45 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.2704-600G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460383 | ||||||
| chr9:95460404
|
G | A | 3 | a0001c0002t0008g0051a0001c0002t0008g0052a0011c0025t0003g0186 | 3 | HG01952.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2704-621C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460404 | ||||||
| chr9:95460416
|
T | C | 1 | a0001c0003t0004g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2704-633A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460416 | ||||||
| chr9:95460467
|
C | T | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2704-684G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460467 | ||||||
| chr9:95460505
|
T | G | 1 | a0002c0001t0009g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2704-722A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460505 | ||||||
| chr9:95460510
|
A | G | 2 | a0001c0002t0008g0051a0001c0002t0008g0052 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2704-727T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460510 | ||||||
| chr9:95460527
|
C | T | 1 | a0001c0003t0035g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2704-744G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460527 | ||||||
| chr9:95460588
|
G | C | 1 | a0001c0002t0021g0233 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2704-805C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460588 | ||||||
| chr9:95460646
|
A | C | 1 | a0001c0004t0002g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2704-863T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460646 | ||||||
| chr9:95460751
|
G | C | 1 | a0002c0036t0036g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2704-968C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460751 | ||||||
| chr9:95461155
|
A | G | 6 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2703+701T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461155 | ||||||
| chr9:95461179
|
T | C | 2 | a0001c0002t0037g0177a0014c0026t0045g0204 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2703+677A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461179 | ||||||
| chr9:95461230
|
A | T | 1 | a0001c0002t0034g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2703+626T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461230 | ||||||
| chr9:95461275
|
C | T | 1 | a0002c0001t0001g0093 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2703+581G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461275 | ||||||
| chr9:95461394
|
C | T | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2703+462G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461394 | ||||||
| chr9:95461416
|
C | T | 1 | a0002c0001t0003g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2703+440G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461416 | ||||||
| chr9:95461455
|
G | T | 3 | a0001c0003t0002g0215a0001c0003t0002g0216a0001c0003t0035g0183 | 3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2703+401C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461455 | ||||||
| chr9:95461556
|
A | G | 1 | a0012c0028t0002g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2703+300T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461556 | ||||||
| chr9:95461560
|
T | C | 1 | a0001c0003t0004g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2703+296A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461560 | ||||||
| chr9:95461574
|
C | T | 11 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(8): Show | 11 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2703+282G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461574 | ||||||
| chr9:95462061
|
G | A | 1 | a0002c0001t0001g0157 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2561-63C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462061 | ||||||
| chr9:95462078
|
C | G | 156 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(153): Show | 166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.2561-80G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462078 | ||||||
| chr9:95462205
|
G | C | 11 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(8): Show | 11 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2561-207C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462205 | ||||||
| chr9:95462345
|
G | A | 11 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(8): Show | 13 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2561-347C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462345 | ||||||
| chr9:95462403
|
A | G | 19 | a0001c0004t0001g0097a0001c0004t0002g0015a0001c0004t0002g0236others(16): Show | 20 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2561-405T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462403 | ||||||
| chr9:95462429
|
T | C | 1 | a0001c0002t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2561-431A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462429 | ||||||
| chr9:95462499
|
G | C | 1 | a0001c0002t0040g0202 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2561-501C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462499 | ||||||
| chr9:95462521
|
A | T | 1 | a0001c0002t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2561-523T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462521 | ||||||
| chr9:95462658
|
G | A | 1 | a0002c0001t0029g0110 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2561-660C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462658 | ||||||
| chr9:95462774
|
G | T | 104 | a0001c0002t0003g0021a0001c0002t0003g0121a0001c0002t0006g0199others(101): Show | 110 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.2561-776C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462774 | ||||||
| chr9:95462832
|
C | A | 1 | a0001c0002t0008g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2561-834G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462832 | ||||||
| chr9:95462941
|
G | A | 3 | a0001c0003t0020g0178a0001c0014t0003g0168a0001c0014t0038g0152 | 3 | HG01081.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2561-943C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462941 | ||||||
| chr9:95462964
|
T | C | 1 | a0009c0015t0001g0085 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2561-966A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462964 | ||||||
| chr9:95462966
|
G | A | 1 | a0001c0003t0020g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2561-968C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462966 | ||||||
| chr9:95462999
|
C | A | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2561-1001G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462999 | ||||||
| chr9:95463007
|
C | T | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2561-1009G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463007 | ||||||
| chr9:95463110
|
G | A | 1 | a0001c0003t0008g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2561-1112C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463110 | ||||||
| chr9:95463125
|
C | T | 3 | a0001c0002t0006g0201a0001c0002t0040g0202a0001c0024t0006g0200 | 3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2561-1127G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463125 | ||||||
| chr9:95463170
|
CA | C | 48 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(45): Show | 51 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.2561-1173delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463170 | ||||||
| chr9:95463187
|
C | T | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2561-1189G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463187 | ||||||
| chr9:95463260
|
G | A | 12 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(9): Show | 13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2561-1262C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463260 | ||||||
| chr9:95463376
|
C | T | 48 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(45): Show | 51 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.2561-1378G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463376 | ||||||
| chr9:95463401
|
C | T | 52 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(49): Show | 56 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.2561-1403G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463401 | ||||||
| chr9:95463425
|
T | C | 1 | a0001c0009t0002g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2561-1427A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463425 | ||||||
| chr9:95463538
|
C | T | 2 | a0002c0035t0001g0173a0002c0036t0036g0109 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2561-1540G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463538 | ||||||
| chr9:95463591
|
T | A | 1 | a0001c0003t0035g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2561-1593A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463591 | ||||||
| chr9:95463681
|
T | C | 1 | a0002c0001t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2561-1683A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463681 | ||||||
| chr9:95463784
|
G | A | 50 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(47): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2561-1786C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463784 | ||||||
| chr9:95463885
|
G | A | 2 | a0001c0002t0002g0196a0001c0002t0002g0197 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2561-1887C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463885 | ||||||
| chr9:95463963
|
C | T | 1 | a0001c0024t0006g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2561-1965G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463963 | ||||||
| chr9:95463969
|
C | T | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2561-1971G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463969 | ||||||
| chr9:95463985
|
C | T | 7 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(4): Show | 9 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2561-1987G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463985 | ||||||
| chr9:95463986
|
G | A | 1 | a0002c0001t0001g0093 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2561-1988C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463986 | ||||||
| chr9:95464025
|
C | T | 44 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(41): Show | 46 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.2561-2027G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464025 | ||||||
| chr9:95464113
|
A | C | 50 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(47): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2561-2115T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464113 | ||||||
| chr9:95464262
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2561-2264T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464262 | ||||||
| chr9:95464420
|
T | C | 50 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(47): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2561-2422A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464420 | ||||||
| chr9:95464748
|
T | C | 2 | a0001c0003t0020g0178a0001c0030t0043g0213 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2560+2368A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464748 | ||||||
| chr9:95464876
|
C | T | 2 | a0002c0001t0001g0086a0002c0001t0001g0164 | 2 | HG01175.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2560+2240G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464876 | ||||||
| chr9:95464951
|
T | C | 27 | a0001c0022t0002g0264a0003c0005t0001g0166a0003c0005t0002g0014others(24): Show | 29 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2560+2165A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464951 | ||||||
| chr9:95465003
|
G | A | 1 | a0001c0002t0034g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2560+2113C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465003 | ||||||
| chr9:95465056
|
G | A | 1 | a0001c0002t0034g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2560+2060C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465056 | ||||||
| chr9:95465133
|
C | T | 50 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(47): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2560+1983G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465133 | ||||||
| chr9:95465451
|
G | A | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2560+1665C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465451 | ||||||
| chr9:95465479
|
C | T | 2 | a0001c0003t0020g0178a0001c0030t0043g0213 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2560+1637G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465479 | ||||||
| chr9:95465505
|
A | G | 1 | a0001c0002t0003g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2560+1611T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465505 | ||||||
| chr9:95465528
|
G | T | 50 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(47): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2560+1588C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465528 | ||||||
| chr9:95465667
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2560+1449C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465667 | ||||||
| chr9:95465719
|
A | G | 1 | a0001c0003t0020g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2560+1397T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465719 | ||||||
| chr9:95465897
|
T | C | 1 | a0002c0001t0001g0148 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2560+1219A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465897 | ||||||
| chr9:95465943
|
C | T | 52 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(49): Show | 56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2560+1173G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465943 | ||||||
| chr9:95466132
|
C | A | 1 | a0001c0003t0020g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2560+984G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466132 | ||||||
| chr9:95466255
|
C | A | 1 | a0001c0002t0023g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2560+861G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466255 | ||||||
| chr9:95466379
|
T | G | 1 | a0001c0002t0001g0106 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2560+737A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466379 | ||||||
| chr9:95466873
|
C | T | 2 | a0003c0005t0005g0074a0003c0005t0005g0122 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2560+243G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466873 | ||||||
| chr9:95466982
|
A | T | 3 | a0001c0002t0001g0106a0002c0001t0001g0135a0016c0034t0003g0134 | 3 | HG01167.hp2 HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2560+134T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466982 | ||||||
| chr9:95467008
|
C | T | 3 | a0001c0003t0002g0215a0001c0003t0002g0216a0001c0003t0035g0183 | 3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2560+108G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467008 | ||||||
| chr9:95467015
|
G | A | 54 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(51): Show | 59 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2560+101C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467015 | ||||||
| chr9:95467084
|
C | T | 3 | a0001c0003t0002g0215a0001c0003t0002g0216a0001c0003t0035g0183 | 3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2560+32G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467084 | ||||||
| chr9:95467107
|
C | G | 154 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(151): Show | 164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.2560+9G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467107 | ||||||
| chr9:95467109
|
G | A | 2 | a0001c0004t0006g0250a0001c0004t0006g0253 | 2 | NA18940.hp2 NA18969.hp2 |
splice_region_variant&intron_variant | LOW | c.2560+7C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467109 | ||||||
| chr9:95467527
|
T | G | 1 | a0001c0003t0035g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2251-102A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95467527 | ||||||
| chr9:95467714
|
G | A | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2251-289C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95467714 | ||||||
| chr9:95468078
|
T | C | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2251-653A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468078 | ||||||
| chr9:95468210
|
G | A | 1 | a0002c0001t0001g0096 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2250+541C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468210 | ||||||
| chr9:95468263
|
C | T | 28 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.2250+488G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468263 | ||||||
| chr9:95468556
|
C | T | 1 | a0002c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2250+195G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468556 | ||||||
| chr9:95468613
|
A | G | 1 | a0001c0003t0004g0036 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2250+138T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468613 | ||||||
| chr9:95468623
|
T | C | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2250+128A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468623 | ||||||
| chr9:95468625
|
T | C | 45 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(42): Show | 47 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.2250+126A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468625 | ||||||
| chr9:95468632
|
C | T | 1 | a0005c0008t0010g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2250+119G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468632 | ||||||
| chr9:95468638
|
C | T | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2250+113G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468638 | ||||||
| chr9:95468642
|
AT | A | 149 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(146): Show | 159 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.2250+108delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468642 | ||||||
| chr9:95468642
|
ATT | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2250+107_2250+108d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468642 | ||||||
| chr9:95468726
|
A | G | 40 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(37): Show | 42 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2250+25T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468726 | ||||||
| chr9:95469321
|
ACCTGGTT others(5): Show |
A | 1 | a0002c0001t0001g0171 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1848-180_1848-169d others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 13/23 | chr9 | 95469321 | ||||||
| chr9:95469553
|
C | T | 2 | a0001c0002t0003g0021a0001c0002t0003g0121 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1847+260G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 13/23 | chr9 | 95469553 | ||||||
| chr9:95469626
|
G | A | 54 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(51): Show | 59 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1847+187C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 13/23 | chr9 | 95469626 | ||||||
| chr9:95470257
|
T | C | 1 | a0005c0008t0010g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1729-326A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470257 | ||||||
| chr9:95470263
|
T | G | 2 | a0001c0004t0002g0261a0002c0011t0002g0241 | 2 | NA18943.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1729-332A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470263 | ||||||
| chr9:95470322
|
T | C | 1 | a0001c0002t0006g0201 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1729-391A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470322 | ||||||
| chr9:95470343
|
T | A | 14 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(11): Show | 15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1729-412A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470343 | ||||||
| chr9:95470410
|
C | A | 3 | a0003c0005t0005g0074a0003c0005t0005g0122a0011c0025t0003g0186 | 3 | HG01952.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1729-479G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470410 | ||||||
| chr9:95470472
|
A | G | 51 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(48): Show | 53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1729-541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470472 | ||||||
| chr9:95470528
|
A | G | 1 | a0002c0001t0029g0110 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1729-597T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470528 | ||||||
| chr9:95470533
|
G | A | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1729-602C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470533 | ||||||
| chr9:95470791
|
G | A | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1729-860C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470791 | ||||||
| chr9:95470812
|
C | T | 1 | a0001c0002t0040g0202 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1729-881G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470812 | ||||||
| chr9:95470908
|
C | T | 1 | a0001c0002t0007g0012 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1729-977G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470908 | ||||||
| chr9:95470916
|
C | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729-985G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470916 | ||||||
| chr9:95470927
|
C | A | 1 | a0001c0002t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1729-996G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470927 | ||||||
| chr9:95471036
|
T | C | 4 | a0001c0002t0010g0181a0005c0008t0010g0011a0005c0008t0010g0179others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729-1105A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471036 | ||||||
| chr9:95471082
|
C | CA | 48 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(45): Show | 51 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1729-1152dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471082 | ||||||
| chr9:95471082
|
CAAAAAAA others(5): Show |
C | 45 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(42): Show | 47 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1729-1163_1729-115 others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471082 | ||||||
| chr9:95471154
|
A | T | 1 | a0002c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1729-1223T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471154 | ||||||
| chr9:95471227
|
G | A | 12 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(9): Show | 13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1729-1296C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471227 | ||||||
| chr9:95471242
|
G | A | 1 | a0001c0003t0013g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1729-1311C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471242 | ||||||
| chr9:95471815
|
A | G | 154 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(151): Show | 164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1729-1884T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471815 | ||||||
| chr9:95471836
|
C | T | 1 | a0002c0001t0001g0096 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1729-1905G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471836 | ||||||
| chr9:95471855
|
A | G | 1 | a0001c0002t0006g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1729-1924T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471855 | ||||||
| chr9:95471998
|
T | C | 1 | a0002c0001t0001g0159 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1729-2067A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471998 | ||||||
| chr9:95472101
|
AAC | A | 12 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(9): Show | 13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1729-2172_1729-217 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472101 | ||||||
| chr9:95472105
|
C | CA | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729-2175dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472105 | ||||||
| chr9:95472105
|
CAG | C | 49 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(46): Show | 52 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1729-2176_1729-217 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472105 | ||||||
| chr9:95472281
|
C | T | 52 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(49): Show | 56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1729-2350G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472281 | ||||||
| chr9:95472310
|
G | C | 3 | a0001c0002t0011g0198a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1729-2379C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472310 | ||||||
| chr9:95472368
|
GT | G | 54 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(51): Show | 59 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1729-2438delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472368 | ||||||
| chr9:95472503
|
C | T | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1729-2572G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472503 | ||||||
| chr9:95472621
|
C | T | 52 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(49): Show | 56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1729-2690G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472621 | ||||||
| chr9:95472663
|
C | T | 1 | a0001c0003t0020g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1729-2732G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472663 | ||||||
| chr9:95472669
|
C | A | 3 | a0001c0002t0011g0198a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1729-2738G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472669 | ||||||
| chr9:95472829
|
C | T | 1 | a0001c0002t0006g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1729-2898G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472829 | ||||||
| chr9:95472966
|
T | C | 4 | a0001c0002t0010g0181a0005c0008t0010g0011a0005c0008t0010g0179others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729-3035A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472966 | ||||||
| chr9:95473028
|
T | C | 51 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(48): Show | 53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728+3006A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473028 | ||||||
| chr9:95473218
|
T | A | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1728+2816A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473218 | ||||||
| chr9:95473447
|
G | A | 3 | a0003c0005t0003g0007a0003c0005t0003g0078a0003c0005t0003g0151 | 4 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728+2587C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473447 | ||||||
| chr9:95473542
|
A | AT | 14 | a0001c0002t0001g0111a0001c0002t0001g0144a0001c0002t0015g0016others(11): Show | 15 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1728+2491dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473542 | ||||||
| chr9:95473542
|
AT | A | 94 | a0001c0002t0001g0150a0001c0002t0002g0196a0001c0002t0002g0197others(91): Show | 99 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1728+2491delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473542 | ||||||
| chr9:95473542
|
ATT | A | 8 | a0001c0004t0002g0242a0001c0007t0002g0205a0001c0007t0002g0206others(5): Show | 8 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1728+2490_1728+249 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473542 | ||||||
| chr9:95473577
|
T | C | 51 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(48): Show | 53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728+2457A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473577 | ||||||
| chr9:95473596
|
G | C | 3 | a0001c0002t0011g0198a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1728+2438C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473596 | ||||||
| chr9:95473603
|
A | G | 51 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(48): Show | 53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728+2431T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473603 | ||||||
| chr9:95473637
|
C | T | 2 | a0001c0002t0002g0196a0001c0002t0002g0197 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1728+2397G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473637 | ||||||
| chr9:95473821
|
C | T | 2 | a0001c0003t0004g0125a0001c0003t0042g0254 | 2 | HG04184.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1728+2213G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473821 | ||||||
| chr9:95473873
|
G | C | 3 | a0003c0031t0003g0185a0007c0012t0003g0019a0007c0012t0003g0020 | 3 | NA18747.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1728+2161C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473873 | ||||||
| chr9:95473879
|
T | C | 1 | a0001c0014t0003g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1728+2155A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473879 | ||||||
| chr9:95473920
|
A | G | 40 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(37): Show | 42 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1728+2114T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473920 | ||||||
| chr9:95474027
|
C | T | 3 | a0001c0002t0007g0012a0001c0002t0007g0193a0001c0002t0007g0194 | 4 | HG02922.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728+2007G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474027 | ||||||
| chr9:95474115
|
A | G | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1728+1919T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474115 | ||||||
| chr9:95474204
|
C | A | 1 | a0001c0004t0021g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1728+1830G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474204 | ||||||
| chr9:95474382
|
C | T | 28 | a0001c0002t0021g0233a0001c0003t0001g0001a0001c0003t0001g0028others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1728+1652G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474382 | ||||||
| chr9:95474583
|
C | T | 44 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(41): Show | 46 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1728+1451G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474583 | ||||||
| chr9:95474760
|
A | G | 1 | a0001c0002t0012g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1728+1274T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474760 | ||||||
| chr9:95474818
|
A | G | 1 | a0002c0001t0001g0010 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1728+1216T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474818 | ||||||
| chr9:95474883
|
G | A | 14 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(11): Show | 15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1728+1151C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474883 | ||||||
| chr9:95475038
|
T | C | 5 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(2): Show | 6 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1728+996A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475038 | ||||||
| chr9:95475169
|
C | T | 1 | a0002c0001t0001g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1728+865G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475169 | ||||||
| chr9:95475171
|
T | C | 2 | a0001c0003t0004g0029a0001c0003t0031g0063 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1728+863A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475171 | ||||||
| chr9:95475280
|
C | T | 1 | a0002c0001t0004g0081 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1728+754G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475280 | ||||||
| chr9:95475514
|
A | G | 145 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(142): Show | 155 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1728+520T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475514 | ||||||
| chr9:95475701
|
A | G | 1 | a0002c0001t0028g0120 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1728+333T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475701 | ||||||
| chr9:95475737
|
T | G | 1 | a0001c0002t0012g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1728+297A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475737 | ||||||
| chr9:95475770
|
T | C | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1728+264A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475770 | ||||||
| chr9:95475995
|
C | T | 1 | a0002c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1728+39G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475995 | ||||||
| chr9:95476217
|
C | G | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603-58G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476217 | ||||||
| chr9:95476219
|
G | C | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603-60C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476219 | ||||||
| chr9:95476328
|
C | T | 1 | a0002c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1603-169G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476328 | ||||||
| chr9:95476566
|
T | C | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1602+193A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476566 | ||||||
| chr9:95476578
|
T | C | 27 | a0001c0022t0002g0264a0003c0005t0001g0166a0003c0005t0002g0014others(24): Show | 29 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1602+181A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476578 | ||||||
| chr9:95476631
|
G | A | 1 | a0015c0033t0005g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1602+128C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476631 | ||||||
| chr9:95476684
|
A | G | 1 | a0001c0002t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+75T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476684 | ||||||
| chr9:95476865
|
A | G | 49 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(46): Show | 52 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(49): Show |
splice_region_variant&intron_variant | LOW | c.1504-8T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95476865 | ||||||
| chr9:95476908
|
G | C | 28 | a0001c0002t0001g0080a0001c0002t0001g0087a0001c0002t0001g0088others(25): Show | 28 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1504-51C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95476908 | ||||||
| chr9:95477144
|
C | T | 1 | a0002c0011t0002g0231 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1504-287G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477144 | ||||||
| chr9:95477151
|
A | C | 1 | a0001c0003t0020g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1504-294T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477151 | ||||||
| chr9:95477221
|
G | A | 44 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(41): Show | 46 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1503+326C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477221 | ||||||
| chr9:95477448
|
G | A | 39 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(36): Show | 41 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1503+99C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477448 | ||||||
| chr9:95477752
|
T | G | 3 | a0001c0002t0011g0198a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1348-50A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 9/23 | chr9 | 95477752 | ||||||
| chr9:95477828
|
T | C | 1 | a0002c0019t0009g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1348-126A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 9/23 | chr9 | 95477828 | ||||||
| chr9:95477838
|
G | A | 154 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(151): Show | 164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1348-136C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 9/23 | chr9 | 95477838 | ||||||
| chr9:95478387
|
G | A | 3 | a0001c0003t0008g0048a0001c0003t0008g0055a0001c0003t0012g0003 | 4 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-201C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478387 | ||||||
| chr9:95478398
|
G | T | 3 | a0003c0005t0002g0228a0006c0016t0001g0124a0006c0023t0011g0229 | 3 | HG00558.hp2 HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1216-212C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478398 | ||||||
| chr9:95478431
|
G | C | 1 | a0001c0007t0002g0207 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1216-245C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478431 | ||||||
| chr9:95478551
|
T | A | 1 | a0001c0002t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1216-365A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478551 | ||||||
| chr9:95478654
|
C | A | 1 | a0007c0012t0003g0019 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1215+346G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478654 | ||||||
| chr9:95478788
|
T | C | 1 | a0011c0025t0003g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1215+212A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478788 | ||||||
| chr9:95478857
|
G | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+143C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478857 | ||||||
| chr9:95478960
|
T | C | 1 | a0001c0003t0020g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1215+40A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478960 | ||||||
| chr9:95478967
|
C | T | 2 | a0002c0001t0001g0090a0002c0001t0001g0157 | 2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1215+33G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478967 | ||||||
| chr9:95479317
|
T | C | 1 | a0001c0002t0002g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1068-170A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479317 | ||||||
| chr9:95479322
|
G | A | 1 | a0001c0003t0020g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1068-175C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479322 | ||||||
| chr9:95479670
|
G | A | 1 | a0011c0025t0003g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1067+299C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479670 | ||||||
| chr9:95479817
|
A | G | 1 | a0001c0003t0020g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1067+152T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479817 | ||||||
| chr9:95479830
|
A | G | 53 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(50): Show | 57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1067+139T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479830 | ||||||
| chr9:95479895
|
T | C | 14 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(11): Show | 15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1067+74A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479895 | ||||||
| chr9:95480193
|
T | G | 1 | a0001c0002t0006g0201 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.946-103A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 6/23 | chr9 | 95480193 | ||||||
| chr9:95480265
|
C | G | 1 | a0001c0002t0023g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.945+125G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 6/23 | chr9 | 95480265 | ||||||
| chr9:95480315
|
A | G | 1 | a0016c0034t0003g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.945+75T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 6/23 | chr9 | 95480315 | ||||||
| chr9:95480643
|
A | G | 53 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(50): Show | 57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.747-55T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480643 | ||||||
| chr9:95480702
|
G | A | 155 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(152): Show | 165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.747-114C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480702 | ||||||
| chr9:95480792
|
C | T | 1 | a0003c0005t0006g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747-204G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480792 | ||||||
| chr9:95480875
|
A | G | 1 | a0001c0002t0006g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.747-287T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480875 | ||||||
| chr9:95480905
|
A | C | 49 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(46): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.747-317T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480905 | ||||||
| chr9:95480907
|
A | AT | 52 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(49): Show | 57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.747-320dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480907 | ||||||
| chr9:95480907
|
AT | A | 76 | a0001c0002t0001g0072a0001c0002t0001g0160a0001c0002t0002g0255others(73): Show | 83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.747-320delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480907 | ||||||
| chr9:95480921
|
A | T | 1 | a0001c0002t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.747-333T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480921 | ||||||
| chr9:95481103
|
A | G | 49 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(46): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.747-515T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481103 | ||||||
| chr9:95481143
|
G | A | 1 | a0001c0003t0020g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.747-555C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481143 | ||||||
| chr9:95481259
|
T | C | 1 | a0001c0003t0004g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.747-671A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481259 | ||||||
| chr9:95481465
|
G | C | 3 | a0001c0004t0002g0244a0001c0004t0002g0245a0001c0004t0002g0252 | 3 | NA18991.hp2 NA19007.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.746+484C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481465 | ||||||
| chr9:95481586
|
C | T | 27 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.746+363G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481586 | ||||||
| chr9:95481638
|
G | A | 1 | a0001c0003t0008g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.746+311C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481638 | ||||||
| chr9:95482266
|
G | A | 2 | a0001c0002t0008g0051a0001c0002t0008g0052 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.585-63C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482266 | ||||||
| chr9:95482301
|
G | T | 1 | a0001c0002t0048g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.585-98C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482301 | ||||||
| chr9:95482326
|
C | T | 1 | a0002c0001t0001g0105 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.585-123G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482326 | ||||||
| chr9:95482329
|
G | A | 1 | a0002c0001t0032g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.585-126C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482329 | ||||||
| chr9:95482338
|
T | C | 3 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207 | 3 | HG00423.hp2 NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.585-135A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482338 | ||||||
| chr9:95482537
|
G | A | 2 | a0001c0002t0002g0196a0001c0002t0002g0197 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.585-334C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482537 | ||||||
| chr9:95482696
|
C | T | 49 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(46): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.585-493G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482696 | ||||||
| chr9:95482726
|
A | G | 1 | a0002c0001t0003g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.585-523T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482726 | ||||||
| chr9:95482744
|
A | G | 27 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.585-541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482744 | ||||||
| chr9:95483093
|
A | G | 1 | a0001c0002t0015g0262 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.585-890T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483093 | ||||||
| chr9:95483109
|
G | GA | 49 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(46): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.585-907dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483109 | ||||||
| chr9:95483264
|
C | CA | 7 | a0001c0002t0006g0199a0001c0002t0007g0012a0001c0002t0007g0191others(4): Show | 8 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-1062dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483264 | ||||||
| chr9:95483264
|
CAA | C | 43 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(40): Show | 45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.585-1063_585-1062d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483264 | ||||||
| chr9:95483373
|
A | G | 1 | a0001c0003t0004g0036 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.585-1170T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483373 | ||||||
| chr9:95483410
|
GA | G | 20 | a0001c0002t0008g0051a0001c0002t0008g0052a0001c0002t0008g0062others(17): Show | 22 | HG00738.hp2 HG01243.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.585-1208delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483410 | ||||||
| chr9:95483425
|
A | AG | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.585-1223_585-1222i others(3): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483425 | ||||||
| chr9:95483434
|
A | G | 13 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(10): Show | 14 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.585-1231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483434 | ||||||
| chr9:95483573
|
T | C | 55 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(52): Show | 60 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.585-1370A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483573 | ||||||
| chr9:95483607
|
C | T | 1 | a0003c0005t0003g0151 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585-1404G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483607 | ||||||
| chr9:95483692
|
A | G | 55 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(52): Show | 60 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.585-1489T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483692 | ||||||
| chr9:95483697
|
T | C | 1 | a0001c0002t0008g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.585-1494A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483697 | ||||||
| chr9:95483748
|
C | T | 1 | a0001c0003t0004g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.585-1545G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483748 | ||||||
| chr9:95483772
|
T | G | 23 | a0001c0022t0002g0264a0003c0005t0001g0166a0003c0005t0002g0014others(20): Show | 25 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.585-1569A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483772 | ||||||
| chr9:95483862
|
T | C | 3 | a0002c0001t0019g0075a0002c0001t0019g0115a0008c0039t0001g0190 | 3 | HG02071.hp1 NA18956.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.585-1659A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483862 | ||||||
| chr9:95484110
|
C | T | 2 | a0001c0002t0001g0172a0013c0027t0001g0169 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.584+1575G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484110 | ||||||
| chr9:95484121
|
A | G | 1 | a0001c0003t0020g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.584+1564T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484121 | ||||||
| chr9:95484236
|
T | C | 2 | a0001c0002t0034g0187a0001c0003t0020g0178 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.584+1449A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484236 | ||||||
| chr9:95484472
|
C | A | 2 | a0001c0002t0001g0172a0013c0027t0001g0169 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.584+1213G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484472 | ||||||
| chr9:95484544
|
C | T | 1 | a0001c0003t0005g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.584+1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484544 | ||||||
| chr9:95484615
|
G | C | 1 | a0004c0006t0005g0123 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.584+1070C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484615 | ||||||
| chr9:95484922
|
C | T | 40 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(37): Show | 42 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.584+763G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484922 | ||||||
| chr9:95484943
|
C | T | 3 | a0001c0002t0011g0198a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.584+742G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484943 | ||||||
| chr9:95485004
|
G | A | 1 | a0002c0011t0002g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.584+681C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485004 | ||||||
| chr9:95485148
|
G | C | 1 | a0002c0001t0001g0116 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.584+537C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485148 | ||||||
| chr9:95485261
|
C | T | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.584+424G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485261 | ||||||
| chr9:95485508
|
C | T | 40 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(37): Show | 42 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.584+177G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485508 | ||||||
| chr9:95486046
|
A | G | 40 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(37): Show | 42 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.395-172T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486046 | ||||||
| chr9:95486105
|
A | G | 49 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(46): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.395-231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486105 | ||||||
| chr9:95486149
|
G | GA | 43 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(40): Show | 45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.395-276_395-275ins others(1): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486149 | ||||||
| chr9:95486353
|
C | A | 154 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(151): Show | 164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.395-479G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486353 | ||||||
| chr9:95486514
|
C | A | 1 | a0001c0003t0008g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.395-640G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486514 | ||||||
| chr9:95486570
|
G | A | 1 | a0001c0004t0021g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.395-696C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486570 | ||||||
| chr9:95487173
|
A | G | 1 | a0001c0003t0013g0024 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.395-1299T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487173 | ||||||
| chr9:95487218
|
G | A | 1 | a0002c0011t0002g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.395-1344C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487218 | ||||||
| chr9:95487267
|
T | C | 1 | a0001c0002t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.395-1393A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487267 | ||||||
| chr9:95487316
|
T | C | 1 | a0002c0001t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.395-1442A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487316 | ||||||
| chr9:95487377
|
A | G | 1 | a0002c0017t0004g0039 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.395-1503T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487377 | ||||||
| chr9:95487681
|
C | T | 37 | a0001c0002t0021g0233a0001c0002t0046g0234a0001c0004t0001g0076others(34): Show | 39 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.395-1807G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487681 | ||||||
| chr9:95487824
|
A | G | 1 | a0001c0003t0013g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.395-1950T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487824 | ||||||
| chr9:95487904
|
T | C | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-2030A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487904 | ||||||
| chr9:95487931
|
A | C | 15 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(12): Show | 16 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.395-2057T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487931 | ||||||
| chr9:95488105
|
A | G | 2 | a0001c0002t0023g0212a0001c0030t0043g0213 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-2231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488105 | ||||||
| chr9:95488293
|
C | G | 2 | a0001c0002t0008g0051a0001c0002t0008g0052 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.395-2419G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488293 | ||||||
| chr9:95488392
|
T | C | 27 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.395-2518A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488392 | ||||||
| chr9:95488415
|
A | G | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-2541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488415 | ||||||
| chr9:95488669
|
A | G | 2 | a0001c0002t0023g0212a0001c0030t0043g0213 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-2795T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488669 | ||||||
| chr9:95488674
|
A | G | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-2800T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488674 | ||||||
| chr9:95488902
|
A | G | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-3028T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488902 | ||||||
| chr9:95489097
|
A | G | 15 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(12): Show | 16 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.395-3223T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489097 | ||||||
| chr9:95489230
|
T | C | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-3356A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489230 | ||||||
| chr9:95489340
|
GT | G | 3 | a0003c0031t0003g0185a0007c0012t0003g0019a0007c0012t0003g0020 | 3 | NA18747.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.395-3467delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489340 | ||||||
| chr9:95489357
|
C | T | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.395-3483G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489357 | ||||||
| chr9:95489381
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.395-3507G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489381 | ||||||
| chr9:95489426
|
G | A | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-3552C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489426 | ||||||
| chr9:95489539
|
C | T | 3 | a0001c0002t0011g0198a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.395-3665G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489539 | ||||||
| chr9:95489602
|
T | G | 1 | a0006c0023t0011g0229 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.395-3728A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489602 | ||||||
| chr9:95489692
|
C | T | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-3818G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489692 | ||||||
| chr9:95489796
|
T | C | 1 | a0002c0001t0001g0070 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.395-3922A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489796 | ||||||
| chr9:95489802
|
A | AT | 22 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(19): Show | 24 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.395-3929dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489802 | ||||||
| chr9:95489917
|
A | C | 1 | a0001c0002t0001g0072 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.395-4043T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489917 | ||||||
| chr9:95489967
|
A | AT | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-4094dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489967 | ||||||
| chr9:95490031
|
T | C | 57 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(54): Show | 62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.395-4157A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490031 | ||||||
| chr9:95490036
|
T | C | 3 | a0001c0003t0008g0048a0001c0003t0008g0055a0001c0003t0012g0003 | 4 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4162A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490036 | ||||||
| chr9:95490044
|
C | T | 1 | a0001c0003t0020g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395-4170G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490044 | ||||||
| chr9:95490270
|
C | T | 1 | a0013c0027t0001g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.395-4396G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490270 | ||||||
| chr9:95490519
|
T | TCACA | 10 | a0001c0002t0016g0017a0001c0003t0020g0178a0003c0005t0002g0217others(7): Show | 11 | HG00609.hp1 HG02056.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACA | 16 | a0001c0002t0023g0256a0001c0030t0043g0213a0003c0005t0001g0166others(13): Show | 18 | HG00558.hp2 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(1): Show |
10 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0062others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(3): Show |
4 | a0001c0002t0008g0052a0001c0002t0011g0198a0003c0005t0011g0227others(1): Show | 4 | HG03098.hp1 NA18979.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(5): Show |
4 | a0001c0002t0023g0212a0003c0005t0005g0074a0003c0005t0005g0122others(1): Show | 4 | HG01081.hp1 HG01952.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(7): Show |
1 | a0001c0013t0025g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.395-4646_395-4645i others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490520
|
G | C | 48 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(45): Show | 51 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.395-4646C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GAC | 19 | a0001c0002t0001g0080a0001c0002t0003g0126a0001c0002t0003g0143others(16): Show | 20 | HG02135.hp2 HG02559.hp1 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.395-4648_395-4647d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACAC | 14 | a0001c0003t0002g0215a0001c0003t0002g0216a0001c0003t0004g0029others(11): Show | 15 | HG00597.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.395-4650_395-4647d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACACAC | 9 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0027others(6): Show | 9 | HG01167.hp1 HG02027.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-4652_395-4647d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACACACA others(1): Show |
5 | a0001c0003t0001g0040a0001c0003t0004g0032a0001c0003t0004g0041others(2): Show | 5 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-4654_395-4647d others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACACACA others(3): Show |
5 | a0001c0003t0004g0042a0001c0003t0004g0043a0001c0003t0004g0044others(2): Show | 5 | HG01099.hp1 HG01192.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-4656_395-4647d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GAC | G | 48 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(45): Show | 52 | HG00140.hp2 HG00558.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.395-4648_395-4647d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GACAC | G | 4 | a0001c0002t0001g0068a0001c0002t0015g0016a0001c0004t0001g0077others(1): Show | 5 | HG00099.hp2 HG01109.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-4650_395-4647d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GACACAC | G | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-4652_395-4647d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GACACACA others(5): Show |
G | 5 | a0001c0002t0001g0072a0002c0001t0001g0070a0002c0001t0001g0073others(2): Show | 6 | HG01106.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-4658_395-4647d others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490529
|
A | ACC | 12 | a0002c0001t0005g0099a0002c0001t0009g0083a0002c0001t0009g0100others(9): Show | 12 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-4656_395-4655i others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490529 | ||||||
| chr9:95490558
|
A | C | 3 | a0001c0002t0037g0177a0001c0022t0002g0264a0014c0026t0045g0204 | 3 | HG02683.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.395-4684T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490558 | ||||||
| chr9:95490565
|
G | A | 155 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(152): Show | 165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.395-4691C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490565 | ||||||
| chr9:95490617
|
C | CA | 7 | a0001c0002t0003g0009a0001c0002t0003g0023a0001c0002t0003g0143others(4): Show | 8 | HG01358.hp1 HG01934.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-4744dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490617 | ||||||
| chr9:95490668
|
A | G | 54 | a0001c0002t0006g0203a0001c0002t0008g0051a0001c0002t0008g0052others(51): Show | 57 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.395-4794T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490668 | ||||||
| chr9:95490759
|
C | G | 12 | a0002c0001t0005g0099a0002c0001t0009g0083a0002c0001t0009g0100others(9): Show | 12 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-4885G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490759 | ||||||
| chr9:95490929
|
C | T | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-5055G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490929 | ||||||
| chr9:95490957
|
C | T | 1 | a0001c0003t0004g0047 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.395-5083G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490957 | ||||||
| chr9:95491121
|
T | C | 5 | a0001c0002t0008g0051a0001c0002t0008g0052a0003c0005t0005g0074others(2): Show | 5 | HG01952.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-5247A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491121 | ||||||
| chr9:95491194
|
G | A | 44 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(41): Show | 46 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.395-5320C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491194 | ||||||
| chr9:95491208
|
C | T | 14 | a0001c0002t0008g0051a0001c0002t0008g0052a0001c0002t0010g0181others(11): Show | 15 | HG01109.hp2 HG01952.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-5334G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491208 | ||||||
| chr9:95491243
|
C | T | 1 | a0002c0001t0032g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.395-5369G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491243 | ||||||
| chr9:95491254
|
G | A | 1 | a0003c0005t0006g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.395-5380C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491254 | ||||||
| chr9:95491380
|
G | A | 1 | a0001c0002t0023g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.395-5506C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491380 | ||||||
| chr9:95491381
|
G | A | 1 | a0001c0002t0012g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.395-5507C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491381 | ||||||
| chr9:95491469
|
C | T | 1 | a0003c0005t0005g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.395-5595G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491469 | ||||||
| chr9:95491477
|
C | T | 1 | a0002c0001t0027g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.395-5603G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491477 | ||||||
| chr9:95491554
|
T | C | 1 | a0001c0003t0035g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.395-5680A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491554 | ||||||
| chr9:95491776
|
C | T | 1 | a0012c0028t0002g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.395-5902G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491776 | ||||||
| chr9:95491903
|
T | C | 1 | a0002c0001t0001g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.395-6029A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491903 | ||||||
| chr9:95491936
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0003g0145a0001c0002t0003g0165 | 3 | HG01071.hp1 HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.395-6062A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491936 | ||||||
| chr9:95491947
|
C | T | 1 | a0013c0027t0001g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.395-6073G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491947 | ||||||
| chr9:95492017
|
A | T | 1 | a0001c0002t0008g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.395-6143T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492017 | ||||||
| chr9:95492040
|
G | A | 1 | a0002c0032t0001g0095 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.395-6166C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492040 | ||||||
| chr9:95492096
|
C | T | 2 | a0001c0003t0002g0215a0001c0003t0002g0216 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-6222G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492096 | ||||||
| chr9:95492190
|
A | G | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.395-6316T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492190 | ||||||
| chr9:95492244
|
C | A | 111 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(108): Show | 119 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.395-6370G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492244 | ||||||
| chr9:95492328
|
G | C | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-6454C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492328 | ||||||
| chr9:95492337
|
T | C | 4 | a0001c0002t0010g0181a0005c0008t0010g0011a0005c0008t0010g0179others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-6463A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492337 | ||||||
| chr9:95492571
|
A | G | 1 | a0011c0025t0003g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.395-6697T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492571 | ||||||
| chr9:95492713
|
G | A | 1 | a0001c0002t0007g0012 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.395-6839C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492713 | ||||||
| chr9:95492821
|
A | AG | 155 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(152): Show | 165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.395-6948_395-6947i others(3): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492821 | ||||||
| chr9:95493156
|
T | C | 32 | a0001c0002t0008g0062a0001c0002t0016g0017a0001c0002t0016g0018others(29): Show | 34 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.395-7282A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493156 | ||||||
| chr9:95493244
|
G | A | 1 | a0002c0001t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.395-7370C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493244 | ||||||
| chr9:95493256
|
A | C | 2 | a0001c0002t0023g0212a0001c0030t0043g0213 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-7382T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493256 | ||||||
| chr9:95493337
|
C | G | 1 | a0003c0005t0011g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.395-7463G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493337 | ||||||
| chr9:95493545
|
A | C | 1 | a0001c0002t0007g0191 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.395-7671T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493545 | ||||||
| chr9:95493746
|
T | C | 1 | a0001c0002t0010g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.395-7872A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493746 | ||||||
| chr9:95493750
|
C | T | 1 | a0001c0003t0013g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.395-7876G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493750 | ||||||
| chr9:95493801
|
C | CA | 18 | a0001c0003t0002g0215a0001c0003t0002g0216a0001c0003t0005g0057others(15): Show | 19 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.395-7928dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493801 | ||||||
| chr9:95493801
|
C | CAA | 25 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(22): Show | 26 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.395-7929_395-7928d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493801 | ||||||
| chr9:95493899
|
G | A | 2 | a0001c0014t0003g0168a0001c0014t0038g0152 | 2 | HG01081.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.395-8025C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493899 | ||||||
| chr9:95493953
|
T | G | 2 | a0001c0002t0003g0118a0002c0001t0003g0127 | 2 | HG01516.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.395-8079A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493953 | ||||||
| chr9:95494027
|
G | A | 43 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(40): Show | 45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.395-8153C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494027 | ||||||
| chr9:95494046
|
C | T | 3 | a0003c0005t0003g0007a0003c0005t0003g0078a0003c0005t0003g0151 | 4 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-8172G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494046 | ||||||
| chr9:95494076
|
A | AACCGCAC others(3): Show |
1 | a0001c0003t0013g0024 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.395-8212_395-8203d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494076 | ||||||
| chr9:95494076
|
AACCGCAC others(3): Show |
A | 5 | a0001c0002t0011g0198a0001c0002t0048g0268a0001c0003t0020g0178others(2): Show | 5 | HG02647.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-8212_395-8203d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494076 | ||||||
| chr9:95494131
|
C | T | 1 | a0001c0002t0016g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.395-8257G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494131 | ||||||
| chr9:95494139
|
C | T | 1 | a0002c0011t0002g0231 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.395-8265G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494139 | ||||||
| chr9:95494158
|
T | A | 19 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.395-8284A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494158 | ||||||
| chr9:95494164
|
G | A | 3 | a0001c0003t0002g0215a0001c0003t0002g0216a0003c0005t0006g0211 | 3 | HG01884.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-8290C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494164 | ||||||
| chr9:95494333
|
C | T | 4 | a0001c0002t0010g0181a0005c0008t0010g0011a0005c0008t0010g0179others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-8459G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494333 | ||||||
| chr9:95494438
|
C | G | 15 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(12): Show | 17 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.395-8564G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494438 | ||||||
| chr9:95494769
|
T | C | 1 | a0001c0002t0001g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.395-8895A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494769 | ||||||
| chr9:95494827
|
C | T | 1 | a0003c0005t0003g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.395-8953G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494827 | ||||||
| chr9:95494886
|
T | C | 1 | a0002c0001t0001g0148 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.395-9012A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494886 | ||||||
| chr9:95495012
|
C | T | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.395-9138G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495012 | ||||||
| chr9:95495023
|
C | T | 35 | a0001c0002t0021g0233a0001c0002t0046g0234a0001c0004t0001g0076others(32): Show | 37 | HG00140.hp2 HG00609.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.395-9149G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495023 | ||||||
| chr9:95495054
|
G | A | 1 | a0003c0005t0006g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.395-9180C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495054 | ||||||
| chr9:95495214
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.395-9340G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495214 | ||||||
| chr9:95495237
|
A | C | 2 | a0001c0003t0004g0029a0001c0003t0031g0063 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.395-9363T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495237 | ||||||
| chr9:95495427
|
C | CT | 17 | a0001c0002t0003g0126a0001c0002t0008g0051a0001c0002t0008g0052others(14): Show | 17 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.395-9554dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495427 | ||||||
| chr9:95495441
|
A | T | 4 | a0001c0002t0016g0017a0001c0002t0016g0018a0001c0002t0037g0177others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-9567T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495441 | ||||||
| chr9:95495502
|
G | A | 1 | a0002c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.395-9628C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495502 | ||||||
| chr9:95495560
|
C | T | 155 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(152): Show | 165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.395-9686G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495560 | ||||||
| chr9:95495646
|
A | G | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.395-9772T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495646 | ||||||
| chr9:95495753
|
T | TG | 8 | a0001c0003t0005g0057a0001c0003t0005g0059a0001c0003t0005g0060others(5): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-9880dupC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495753 | ||||||
| chr9:95496084
|
T | C | 1 | a0001c0003t0005g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.395-10210A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496084 | ||||||
| chr9:95496128
|
C | A | 1 | a0001c0003t0004g0046 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.395-10254G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496128 | ||||||
| chr9:95496199
|
C | G | 1 | a0003c0005t0002g0228 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.394+10208G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496199 | ||||||
| chr9:95496537
|
T | TA | 21 | a0001c0002t0023g0256a0001c0022t0002g0264a0002c0001t0047g0265others(18): Show | 23 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.394+9869dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496537 | ||||||
| chr9:95496979
|
G | A | 2 | a0001c0002t0023g0212a0001c0030t0043g0213 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.394+9428C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496979 | ||||||
| chr9:95497421
|
T | G | 133 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(130): Show | 141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.394+8986A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497421 | ||||||
| chr9:95497489
|
CT | C | 133 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(130): Show | 141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.394+8917delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497489 | ||||||
| chr9:95497951
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.394+8456G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497951 | ||||||
| chr9:95497967
|
G | A | 8 | a0001c0002t0010g0181a0001c0003t0020g0178a0001c0003t0020g0182others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.394+8440C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497967 | ||||||
| chr9:95498232
|
G | A | 133 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(130): Show | 141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.394+8175C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498232 | ||||||
| chr9:95498273
|
T | C | 8 | a0001c0002t0015g0016a0001c0002t0015g0262a0001c0002t0034g0187others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+8134A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498273 | ||||||
| chr9:95498656
|
T | C | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394+7751A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498656 | ||||||
| chr9:95498729
|
G | T | 2 | a0001c0013t0025g0266a0001c0013t0025g0267 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394+7678C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498729 | ||||||
| chr9:95498750
|
C | A | 17 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.394+7657G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498750 | ||||||
| chr9:95499108
|
C | T | 1 | a0001c0004t0002g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394+7299G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499108 | ||||||
| chr9:95499519
|
G | C | 4 | a0001c0002t0010g0181a0005c0008t0010g0011a0005c0008t0010g0179others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+6888C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499519 | ||||||
| chr9:95499783
|
C | G | 1 | a0001c0002t0006g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.394+6624G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499783 | ||||||
| chr9:95499896
|
G | A | 43 | a0001c0002t0003g0056a0001c0002t0008g0051a0001c0002t0008g0052others(40): Show | 46 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.394+6511C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499896 | ||||||
| chr9:95499908
|
C | G | 6 | a0001c0002t0003g0121a0001c0014t0003g0168a0001c0014t0038g0152others(3): Show | 7 | HG01081.hp2 HG02970.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+6499G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499908 | ||||||
| chr9:95499941
|
G | A | 46 | a0001c0002t0003g0056a0001c0002t0008g0051a0001c0002t0008g0052others(43): Show | 49 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.394+6466C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499941 | ||||||
| chr9:95500002
|
C | A | 2 | a0001c0002t0037g0177a0014c0026t0045g0204 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.394+6405G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500002 | ||||||
| chr9:95500035
|
G | A | 1 | a0001c0002t0003g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.394+6372C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500035 | ||||||
| chr9:95500116
|
G | A | 1 | a0001c0002t0007g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394+6291C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500116 | ||||||
| chr9:95500213
|
A | G | 1 | a0002c0001t0003g0071 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.394+6194T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500213 | ||||||
| chr9:95500350
|
T | C | 3 | a0001c0007t0022g0208a0001c0038t0044g0210a0010c0018t0022g0209 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.394+6057A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500350 | ||||||
| chr9:95500353
|
C | T | 1 | a0001c0004t0002g0260 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.394+6054G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500353 | ||||||
| chr9:95500453
|
A | G | 62 | a0001c0002t0002g0255a0001c0002t0003g0175a0001c0002t0015g0016others(59): Show | 66 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.394+5954T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500453 | ||||||
| chr9:95500551
|
A | G | 134 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(131): Show | 142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.394+5856T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500551 | ||||||
| chr9:95500575
|
C | T | 1 | a0001c0002t0001g0150 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.394+5832G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500575 | ||||||
| chr9:95500654
|
G | A | 1 | a0001c0004t0021g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.394+5753C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500654 | ||||||
| chr9:95500747
|
C | T | 16 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(13): Show | 17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+5660G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500747 | ||||||
| chr9:95500838
|
T | C | 2 | a0001c0003t0020g0182a0001c0003t0035g0183 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.394+5569A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500838 | ||||||
| chr9:95500856
|
A | C | 17 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.394+5551T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500856 | ||||||
| chr9:95500950
|
C | T | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.394+5457G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500950 | ||||||
| chr9:95500961
|
G | A | 1 | a0001c0002t0005g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.394+5446C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500961 | ||||||
| chr9:95501063
|
T | C | 1 | a0001c0002t0006g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394+5344A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501063 | ||||||
| chr9:95501174
|
C | A | 17 | a0001c0022t0002g0264a0003c0005t0002g0014a0003c0005t0002g0217others(14): Show | 19 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+5233G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501174 | ||||||
| chr9:95501375
|
G | C | 2 | a0001c0002t0003g0167a0001c0003t0031g0063 | 2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.394+5032C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501375 | ||||||
| chr9:95501539
|
T | TA | 100 | a0001c0002t0002g0255a0001c0002t0003g0056a0001c0002t0003g0175others(97): Show | 107 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.394+4867dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501539 | ||||||
| chr9:95501539
|
TAAA | T | 18 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(15): Show | 19 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.394+4865_394+4867d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501539 | ||||||
| chr9:95501588
|
G | A | 16 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(13): Show | 17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+4819C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501588 | ||||||
| chr9:95501985
|
A | G | 1 | a0003c0005t0002g0217 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.394+4422T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501985 | ||||||
| chr9:95502055
|
G | C | 3 | a0001c0003t0005g0059a0001c0003t0005g0060a0001c0003t0005g0061 | 3 | HG03195.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.394+4352C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502055 | ||||||
| chr9:95502090
|
A | G | 8 | a0001c0002t0015g0016a0001c0002t0015g0262a0001c0002t0034g0187others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+4317T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502090 | ||||||
| chr9:95502236
|
G | A | 2 | a0003c0005t0002g0228a0006c0023t0011g0229 | 2 | HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.394+4171C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502236 | ||||||
| chr9:95502466
|
C | A | 1 | a0002c0001t0017g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.394+3941G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502466 | ||||||
| chr9:95502660
|
A | C | 46 | a0001c0002t0003g0056a0001c0002t0008g0051a0001c0002t0008g0052others(43): Show | 49 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.394+3747T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502660 | ||||||
| chr9:95502666
|
A | C | 17 | a0001c0022t0002g0264a0003c0005t0002g0014a0003c0005t0002g0217others(14): Show | 19 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+3741T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502666 | ||||||
| chr9:95502722
|
C | A | 17 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.394+3685G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502722 | ||||||
| chr9:95502869
|
G | A | 1 | a0001c0004t0002g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394+3538C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502869 | ||||||
| chr9:95502894
|
C | T | 1 | a0002c0001t0028g0120 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394+3513G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502894 | ||||||
| chr9:95502907
|
G | A | 2 | a0001c0003t0013g0049a0001c0003t0013g0050 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.394+3500C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502907 | ||||||
| chr9:95502936
|
C | T | 6 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+3471G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502936 | ||||||
| chr9:95503243
|
G | A | 1 | a0001c0004t0002g0260 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.394+3164C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503243 | ||||||
| chr9:95503380
|
C | A | 3 | a0001c0002t0048g0268a0001c0013t0025g0266a0001c0013t0025g0267 | 3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.394+3027G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503380 | ||||||
| chr9:95503405
|
G | A | 1 | a0001c0002t0008g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.394+3002C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503405 | ||||||
| chr9:95503498
|
C | T | 134 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(131): Show | 142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.394+2909G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503498 | ||||||
| chr9:95503551
|
G | T | 1 | a0001c0003t0004g0047 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.394+2856C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503551 | ||||||
| chr9:95503619
|
A | G | 46 | a0001c0002t0003g0056a0001c0002t0008g0051a0001c0002t0008g0052others(43): Show | 49 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.394+2788T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503619 | ||||||
| chr9:95503732
|
TAGGGCCG others(322): Show |
T | 142 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(139): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.394+2346_394+2674d others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503732 | ||||||
| chr9:95504022
|
C | CA | 6 | a0001c0002t0001g0172a0001c0014t0003g0168a0002c0001t0001g0010others(3): Show | 7 | HG00408.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+2384dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
C | CAAAAAAA others(6): Show |
1 | a0002c0035t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394+2372_394+2384d others(15): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CA | C | 34 | a0001c0002t0001g0128a0001c0002t0001g0144a0001c0002t0003g0121others(31): Show | 34 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.394+2384delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAA | C | 32 | a0001c0002t0001g0068a0001c0002t0001g0106a0001c0002t0001g0107others(29): Show | 35 | HG00099.hp1 HG01106.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.394+2383_394+2384d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAA | C | 17 | a0001c0002t0001g0087a0001c0002t0001g0088a0002c0001t0001g0082others(14): Show | 17 | HG01069.hp2 HG01175.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+2382_394+2384d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0001t0004g0081 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.394+2374_394+2384d others(13): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0002t0001g0080a0001c0004t0001g0079 | 2 | HG03492.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.394+2369_394+2384d others(18): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(10): Show |
C | 1 | a0003c0005t0003g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.394+2368_394+2384d others(19): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(11): Show |
C | 3 | a0001c0002t0016g0018a0001c0004t0001g0076a0001c0004t0001g0077 | 3 | HG00099.hp2 HG03471.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.394+2367_394+2384d others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0002t0016g0017a0002c0001t0019g0075 | 2 | HG02071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.394+2366_394+2384d others(21): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(14): Show |
C | 1 | a0003c0005t0005g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394+2364_394+2384d others(23): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504056
|
A | C | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.394+2351T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504056 | ||||||
| chr9:95504061
|
A | T | 2 | a0001c0002t0016g0017a0001c0002t0016g0018 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.394+2346T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504061 | ||||||
| chr9:95504088
|
A | G | 134 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(131): Show | 142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.394+2319T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504088 | ||||||
| chr9:95504380
|
G | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+2027C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504380 | ||||||
| chr9:95504573
|
T | A | 47 | a0001c0002t0003g0056a0001c0002t0008g0051a0001c0002t0008g0052others(44): Show | 50 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.394+1834A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504573 | ||||||
| chr9:95505066
|
G | A | 1 | a0010c0018t0022g0209 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.394+1341C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505066 | ||||||
| chr9:95505141
|
G | A | 24 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(21): Show | 26 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.394+1266C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505141 | ||||||
| chr9:95505266
|
C | T | 2 | a0001c0003t0013g0049a0001c0003t0013g0050 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.394+1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505266 | ||||||
| chr9:95505300
|
G | A | 1 | a0001c0030t0043g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394+1107C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505300 | ||||||
| chr9:95505359
|
G | A | 1 | a0002c0001t0001g0174 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.394+1048C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505359 | ||||||
| chr9:95505361
|
A | T | 5 | a0001c0002t0001g0072a0002c0001t0001g0070a0002c0001t0001g0073others(2): Show | 6 | HG01106.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+1046T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505361 | ||||||
| chr9:95505464
|
T | G | 142 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(139): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.394+943A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505464 | ||||||
| chr9:95505488
|
G | A | 1 | a0001c0002t0007g0195 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.394+919C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505488 | ||||||
| chr9:95505833
|
T | C | 1 | a0001c0003t0004g0047 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.394+574A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505833 | ||||||
| chr9:95505881
|
G | T | 6 | a0001c0002t0007g0012a0001c0002t0007g0191a0001c0002t0007g0192others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+526C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505881 | ||||||
| chr9:95505918
|
C | A | 1 | a0001c0004t0002g0261 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.394+489G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505918 | ||||||
| chr9:95505983
|
C | T | 1 | a0002c0020t0001g0069 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.394+424G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505983 | ||||||
| chr9:95506114
|
G | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+293C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506114 | ||||||
| chr9:95506192
|
C | G | 1 | a0001c0003t0008g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394+215G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506192 | ||||||
| chr9:95506195
|
G | T | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+212C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506195 | ||||||
| chr9:95506336
|
T | C | 2 | a0001c0002t0015g0016a0001c0002t0015g0262 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.394+71A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506336 | ||||||
| chr9:95506656
|
A | ACGCCCGC others(11): Show |
24 | a0001c0003t0001g0001a0001c0003t0001g0028a0001c0003t0001g0040others(21): Show | 25 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.202-75_202-58dupGG others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95506656 | ||||||
| chr9:95506816
|
G | A | 6 | a0001c0007t0002g0205a0001c0007t0002g0206a0001c0007t0002g0207others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-217C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95506816 | ||||||
| chr9:95507136
|
CG | C | 86 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(83): Show | 91 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.202-538delC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507136 | ||||||
| chr9:95507156
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.202-557G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507156 | ||||||
| chr9:95507208
|
G | C | 1 | a0001c0002t0001g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.202-609C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507208 | ||||||
| chr9:95507381
|
G | A | 3 | a0001c0002t0006g0201a0001c0002t0040g0202a0001c0024t0006g0200 | 3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.201+780C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507381 | ||||||
| chr9:95507433
|
T | A | 1 | a0002c0011t0002g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.201+728A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507433 | ||||||
| chr9:95507655
|
A | C | 1 | a0001c0003t0004g0025 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.201+506T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507655 | ||||||
| chr9:95507757
|
T | C | 4 | a0001c0002t0006g0199a0001c0002t0006g0201a0001c0002t0040g0202others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+404A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507757 | ||||||
| chr9:95507764
|
C | T | 4 | a0001c0002t0005g0066a0002c0001t0001g0064a0002c0001t0001g0067others(1): Show | 4 | HG02559.hp2 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+397G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507764 | ||||||
| chr9:95507792
|
A | T | 1 | a0001c0003t0031g0063 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.201+369T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507792 | ||||||
| chr9:95507886
|
A | G | 133 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(130): Show | 141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.201+275T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507886 | ||||||
| chr9:95507889
|
A | G | 143 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(140): Show | 152 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.201+272T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507889 | ||||||
| chr9:95507905
|
T | TAC | 13 | a0001c0002t0010g0181a0001c0002t0016g0017a0001c0002t0016g0018others(10): Show | 14 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+254_201+255dup others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507905 | ||||||
| chr9:95507905
|
T | TACAC | 126 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0255others(123): Show | 134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.201+252_201+255dup others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507905 | ||||||
| chr9:95507905
|
T | TACACAC | 3 | a0001c0002t0008g0062a0001c0003t0005g0061a0001c0022t0002g0264 | 3 | HG02257.hp1 HG02683.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.201+250_201+255dup others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507905 | ||||||
| chr9:95508034
|
TGTGA | T | 50 | a0001c0002t0003g0056a0001c0002t0006g0203a0001c0002t0008g0051others(47): Show | 53 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.201+123_201+126del others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508034 | ||||||
| chr9:95508038
|
AGTGAGTG others(1): Show |
A | 63 | a0001c0002t0002g0255a0001c0002t0015g0016a0001c0002t0015g0262others(60): Show | 67 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.201+115_201+122del others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508038 | ||||||
| chr9:95508040
|
TGA | T | 14 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(11): Show | 15 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.201+119_201+120del others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508040 | ||||||
| chr9:95508042
|
A | T | 7 | a0001c0002t0003g0023a0001c0007t0002g0205a0001c0007t0002g0206others(4): Show | 7 | HG00423.hp2 HG01358.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+119T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508042 | ||||||
| chr9:95508060
|
A | T | 17 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0003g0021others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.201+101T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508060 |