Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8643 |
| ensemblid | ENSG00000117425.14 |
| hgncid | 9586 |
| symbol | PTCH2 |
| name | patched 2 |
| refseq_nuc | NM_003738.5 |
| refseq_prot | NP_003729.3 |
| ensembl_nuc | ENST00000372192.4 |
| ensembl_prot | ENSP00000361266.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 44821938 |
| end | 44843253 |
| strand | - |
| ver | v1.2 |
| region | chr1:44821938-44843253 |
| region5000 | chr1:44816938-44848253 |
| regionname0 | PTCH2_chr1_44821938_44843253 |
| regionname5000 | PTCH2_chr1_44816938_44848253 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1203 | 329 | 86 | 53 | 137 | 16 | 35 | 99 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0002 | 0/0 | 1203 | 33 | 0 | 6 | 26 | 0 | 1 | 22 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0003 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0004 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0005 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0006 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0008 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0009 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| a0010 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | MTRSP others(1198): Show |
chr1 | 44816938 | 44848253 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3609 | 169 | 36 | 32 | 67 | 9 | 24 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0002 | 0/0 | 3609 | 67 | 10 | 12 | 36 | 4 | 5 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0003 | 0/1 | 3609 | 50 | 12 | 6 | 22 | 3 | 6 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0005 | 0/0 | 3609 | 23 | 22 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0007 | 0/0 | 3609 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0008 | 0/0 | 3609 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0010 | 0/0 | 3609 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0011 | 0/0 | 3609 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0012 | 0/0 | 3609 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0016 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0017 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0019 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0020 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0021 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0001c0023 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0002c0004 | 0/0 | 3609 | 25 | 0 | 2 | 22 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0002c0006 | 0/0 | 3609 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0002c0009 | 0/0 | 3609 | 3 | 0 | 3 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0002c0024 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0003c0018 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0004c0014 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0005c0025 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0006c0015 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0007c0026 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0008c0027 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0009c0022 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 | ||
| a0010c0013 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | ATGAC others(3604): Show |
chr1 | 44816938 | 44848253 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4410 | 167 | 34 | 32 | 67 | 9 | 24 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0001t0003 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0001t0005 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0002t0001 | 0/0 | 4410 | 67 | 10 | 12 | 36 | 4 | 5 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0003t0001 | 0/1 | 4410 | 49 | 12 | 6 | 21 | 3 | 6 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0003t0007 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0005t0001 | 0/0 | 4410 | 23 | 22 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0007t0001 | 0/0 | 4410 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0008t0001 | 0/0 | 4410 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0010t0002 | 0/0 | 4410 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0010t0006 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0011t0001 | 0/0 | 4410 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0012t0001 | 0/0 | 4410 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0016t0001 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0017t0001 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0019t0001 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0020t0001 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0021t0001 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0001c0023t0002 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0002c0004t0001 | 0/0 | 4410 | 25 | 0 | 2 | 22 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0002c0006t0001 | 0/0 | 4410 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0002c0009t0001 | 0/0 | 4410 | 3 | 0 | 3 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0002c0024t0001 | 0/0 | 4410 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0003c0018t0004 | 0/0 | 4410 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0004c0014t0001 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0005c0025t0001 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0006c0015t0001 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0007c0026t0001 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0008c0027t0001 | 0/0 | 4410 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0009c0022t0001 | 0/0 | 4410 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| a0010c0013t0001 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | GCAGT others(4405): Show |
chr1 | 44816938 | 44848253 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 39 | 3 | 5 | 25 | 1 | 5 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0003 | 0/0 | 11 | 1 | 4 | 1 | 3 | 2 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0005 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0002 | 0/0 | 15 | 1 | 2 | 9 | 1 | 2 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0004 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0003t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0007t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0010t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0010t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0011t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0011t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0012t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0012t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0016t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0017t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0019t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0020t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0021t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0001c0023t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0009t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0009t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0002c0024t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0003c0018t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0004c0014t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0005c0025t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0006c0015t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0007c0026t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0008c0027t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0009c0022t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| a0010c0013t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0187 | EUR | FIN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0176 | EUR | FIN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0200 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00621 | hp2 | a0002 | c0004 | t0001 | g0152 | EAS | CHS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01099 | hp2 | a0002 | c0009 | t0001 | g0035 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01109 | hp1 | a0001 | c0011 | t0001 | g0055 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01167 | hp1 | a0001 | c0005 | t0001 | g0140 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01255 | hp2 | a0001 | c0011 | t0001 | g0083 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0162 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01261 | hp1 | a0002 | c0024 | t0001 | g0155 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01358 | hp2 | a0002 | c0009 | t0001 | g0035 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0196 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0047 | EUR | IBS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0047 | EUR | IBS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0141 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01891 | hp2 | a0001 | c0021 | t0001 | g0217 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01975 | hp2 | a0002 | c0009 | t0001 | g0153 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01978 | hp2 | a0002 | c0004 | t0001 | g0173 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01993 | hp1 | a0003 | c0018 | t0004 | g0081 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0202 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0138 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02083 | hp1 | a0002 | c0004 | t0001 | g0178 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02129 | hp2 | a0001 | c0003 | t0007 | g0242 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02132 | hp2 | a0002 | c0004 | t0001 | g0177 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | CDX | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02258 | hp2 | a0001 | c0017 | t0001 | g0203 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PEL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02280 | hp2 | a0004 | c0014 | t0001 | g0076 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | KHV | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0146 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0137 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0148 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0149 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0184 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0136 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03098 | hp1 | a0005 | c0025 | t0001 | g0139 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03098 | hp2 | a0001 | c0023 | t0002 | g0049 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0143 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03130 | hp2 | a0001 | c0010 | t0006 | g0241 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03139 | hp2 | a0006 | c0015 | t0001 | g0144 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03225 | hp1 | a0007 | c0026 | t0001 | g0233 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0194 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0033 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0033 | AFR | ESN | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0169 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | STU | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0038 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03831 | hp2 | a0008 | c0027 | t0001 | g0240 | SAS | BEB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03834 | hp2 | a0002 | c0004 | t0001 | g0034 | SAS | BEB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03942 | hp2 | a0009 | c0022 | t0001 | g0174 | SAS | BEB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0191 | SAS | STU | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0170 | SAS | STU | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | YRI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | CHB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18612 | hp2 | a0002 | c0004 | t0001 | g0167 | EAS | CHB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | CHB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | YRI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18940 | hp2 | a0002 | c0006 | t0001 | g0206 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18942 | hp1 | a0010 | c0013 | t0001 | g0209 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18944 | hp1 | a0001 | c0020 | t0001 | g0230 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18944 | hp2 | a0001 | c0008 | t0001 | g0135 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18947 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18951 | hp1 | a0002 | c0004 | t0001 | g0185 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18951 | hp2 | a0001 | c0007 | t0001 | g0025 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18953 | hp1 | a0002 | c0004 | t0001 | g0238 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18954 | hp2 | a0001 | c0007 | t0001 | g0091 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18956 | hp2 | a0001 | c0012 | t0001 | g0226 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18959 | hp2 | a0002 | c0004 | t0001 | g0165 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18960 | hp1 | a0001 | c0019 | t0001 | g0197 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18969 | hp2 | a0001 | c0008 | t0001 | g0134 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18972 | hp1 | a0002 | c0004 | t0001 | g0189 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18980 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18980 | hp2 | a0001 | c0007 | t0001 | g0025 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18981 | hp1 | a0002 | c0004 | t0001 | g0154 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18981 | hp2 | a0001 | c0007 | t0001 | g0093 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18984 | hp1 | a0002 | c0004 | t0001 | g0168 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18986 | hp2 | a0002 | c0004 | t0001 | g0236 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18989 | hp2 | a0001 | c0008 | t0001 | g0132 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18999 | hp1 | a0002 | c0004 | t0001 | g0183 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19000 | hp1 | a0002 | c0004 | t0001 | g0175 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19001 | hp1 | a0002 | c0004 | t0001 | g0207 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19009 | hp1 | a0002 | c0006 | t0001 | g0171 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | LWK | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | LWK | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19054 | hp1 | a0002 | c0006 | t0001 | g0150 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19058 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19063 | hp2 | a0001 | c0012 | t0001 | g0228 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19064 | hp2 | a0001 | c0016 | t0001 | g0099 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19068 | hp1 | a0002 | c0004 | t0001 | g0188 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19076 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19077 | hp2 | a0002 | c0004 | t0001 | g0131 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19087 | hp2 | a0002 | c0004 | t0001 | g0156 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19091 | hp1 | a0002 | c0006 | t0001 | g0159 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | YRI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20129 | hp1 | a0001 | c0010 | t0002 | g0015 | AFR | ASW | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | ASW | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0038 | EUR | TSI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0045 | EUR | TSI | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0034 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | ACB | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0142 | AFR | MSL | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | USA | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA18955 | hp2 | a0002 | c0004 | t0001 | g0172 | EAS | JPT | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | USA | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA20300 | hp2 | a0001 | c0010 | t0002 | g0015 | AFR | USA | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0180 | REF | REF | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0084 | REF | REF | PTCH2_chr1_44816938_44848253 | PTCH2 | chr1 | 44816938 | 44848253 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44826258 | C | T | 1 | a0003 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.3106G>A | p.Val1036Met | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/22 | 3427/4410 | 3106/3612 | 1036/1203 | chr1 | 44826258 | |||
| chr1:44826501 | G | A | 1 | a0002 | 33 | HG00621.hp2 HG01099.hp2 HG01123.hp1 others(30): Show |
missense_variant | MODERATE | c.2963C>T | p.Thr988Met | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 18/22 | 3284/4410 | 2963/3612 | 988/1203 | chr1 | 44826501 | |||
| chr1:44826562 | C | T | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2902G>A | p.Val968Ile | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 18/22 | 3223/4410 | 2902/3612 | 968/1203 | chr1 | 44826562 | |||
| chr1:44826765 | G | A | 1 | a0003 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2699C>T | p.Pro900Leu | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 18/22 | 3020/4410 | 2699/3612 | 900/1203 | chr1 | 44826765 | |||
| chr1:44827907 | C | T | 2 | a0006 a0007 |
2 | HG03139.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.1994G>A | p.Arg665His | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 14/22 | 2315/4410 | 1994/3612 | 665/1203 | chr1 | 44827907 | |||
| chr1:44828628 | G | A | 1 | a0009 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1468C>T | p.Arg490Cys | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 12/22 | 1789/4410 | 1468/3612 | 490/1203 | chr1 | 44828628 | |||
| chr1:44829709 | C | T | 1 | a0004 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.988G>A | p.Glu330Lys | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 8/22 | 1309/4410 | 988/3612 | 330/1203 | chr1 | 44829709 | |||
| chr1:44831039 | G | A | 1 | a0005 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.622C>T | p.Arg208Cys | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/22 | 943/4410 | 622/3612 | 208/1203 | chr1 | 44831039 | |||
| chr1:44832296 | A | G | 1 | a0010 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.311T>C | p.Leu104Pro | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 3/22 | 632/4410 | 311/3612 | 104/1203 | chr1 | 44832296 | |||
| chr1:44842889 | G | A | 1 | a0008 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.44C>T | p.Thr15Ile | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/22 | 365/4410 | 44/3612 | 15/1203 | chr1 | 44842889 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44823284 | A | G | 1 | a0001c0017 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.3216T>C | p.Gly1072Gly | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 20/22 | 3537/4410 | 3216/3612 | 1072/1203 | chr1 | 44823284 | |||
| chr1:44826927 | G | A | 1 | a0001c0019 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.2670C>T | p.Tyr890Tyr | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 17/22 | 2991/4410 | 2670/3612 | 890/1203 | chr1 | 44826927 | |||
| chr1:44827032 | G | A | 2 | a0002c0009 a0002c0024 |
4 | HG01099.hp2 HG01261.hp1 HG01358.hp2 others(1): Show |
synonymous_variant | LOW | c.2565C>T | p.Leu855Leu | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 17/22 | 2886/4410 | 2565/3612 | 855/1203 | chr1 | 44827032 | |||
| chr1:44827038 | G | A | 1 | a0007c0026 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.2559C>T | p.Pro853Pro | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 17/22 | 2880/4410 | 2559/3612 | 853/1203 | chr1 | 44827038 | |||
| chr1:44827194 | G | A | 5 | a0001c0002 a0001c0012 a0001c0016 others(2): Show |
72 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(69): Show |
synonymous_variant | LOW | c.2487C>T | p.Asp829Asp | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 16/22 | 2808/4410 | 2487/3612 | 829/1203 | chr1 | 44827194 | |||
| chr1:44827254 | C | G | 1 | a0001c0011 | 2 | HG01109.hp1 HG01255.hp2 |
synonymous_variant | LOW | c.2427G>C | p.Ser809Ser | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 16/22 | 2748/4410 | 2427/3612 | 809/1203 | chr1 | 44827254 | |||
| chr1:44827418 | G | A | 2 | a0001c0017 a0007c0026 |
2 | HG02258.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.2355C>T | p.Tyr785Tyr | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 15/22 | 2676/4410 | 2355/3612 | 785/1203 | chr1 | 44827418 | |||
| chr1:44827631 | C | T | 1 | a0001c0016 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.2142G>A | p.Thr714Thr | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 15/22 | 2463/4410 | 2142/3612 | 714/1203 | chr1 | 44827631 | |||
| chr1:44827712 | G | A | 1 | a0010c0013 | 1 | NA18942.hp1 | splice_region_variant&synonymous_variant | LOW | c.2061C>T | p.Ala687Ala | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 15/22 | 2382/4410 | 2061/3612 | 687/1203 | chr1 | 44827712 | |||
| chr1:44827846 | A | G | 21 | a0001c0002 a0001c0003 a0001c0005 others(18): Show |
191 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
synonymous_variant | LOW | c.2055T>C | p.Ala685Ala | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 14/22 | 2376/4410 | 2055/3612 | 685/1203 | chr1 | 44827846 | |||
| chr1:44828080 | T | C | 10 | a0001c0003 a0001c0010 a0001c0019 others(7): Show |
89 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.1821A>G | p.Glu607Glu | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 14/22 | 2142/4410 | 1821/3612 | 607/1203 | chr1 | 44828080 | |||
| chr1:44828563 | G | A | 1 | a0001c0020 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.1533C>T | p.Ala511Ala | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 12/22 | 1854/4410 | 1533/3612 | 511/1203 | chr1 | 44828563 | |||
| chr1:44828590 | G | A | 1 | a0001c0021 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1506C>T | p.Val502Val | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 12/22 | 1827/4410 | 1506/3612 | 502/1203 | chr1 | 44828590 | |||
| chr1:44829015 | G | A | 1 | a0002c0006 | 4 | NA18940.hp2 NA19009.hp1 NA19054.hp1 others(1): Show |
synonymous_variant | LOW | c.1431C>T | p.Ala477Ala | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 11/22 | 1752/4410 | 1431/3612 | 477/1203 | chr1 | 44829015 | |||
| chr1:44830004 | A | G | 1 | a0001c0008 | 3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
synonymous_variant | LOW | c.840T>C | p.Ser280Ser | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 7/22 | 1161/4410 | 840/3612 | 280/1203 | chr1 | 44830004 | |||
| chr1:44830923 | G | A | 1 | a0001c0012 | 2 | NA18956.hp2 NA19063.hp2 |
synonymous_variant | LOW | c.738C>T | p.Ala246Ala | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/22 | 1059/4410 | 738/3612 | 246/1203 | chr1 | 44830923 | |||
| chr1:44830974 | G | A | 2 | a0001c0010 a0001c0023 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
synonymous_variant | LOW | c.687C>T | p.Ala229Ala | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/22 | 1008/4410 | 687/3612 | 229/1203 | chr1 | 44830974 | |||
| chr1:44831037 | G | A | 1 | a0002c0024 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.624C>T | p.Arg208Arg | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/22 | 945/4410 | 624/3612 | 208/1203 | chr1 | 44831037 | |||
| chr1:44831717 | G | A | 1 | a0007c0026 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.606C>T | p.Ser202Ser | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 5/22 | 927/4410 | 606/3612 | 202/1203 | chr1 | 44831717 | |||
| chr1:44831720 | G | C | 1 | a0001c0007 | 4 | NA18951.hp2 NA18954.hp2 NA18980.hp2 others(1): Show |
synonymous_variant | LOW | c.603C>G | p.Gly201Gly | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 5/22 | 924/4410 | 603/3612 | 201/1203 | chr1 | 44831720 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44822087 | C | A | 1 | a0001c0001t0005 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 22/22 | 328 | chr1 | 44822087 | ||||||
| chr1:44822278 | C | T | 1 | a0003c0018t0004 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 22/22 | 137 | chr1 | 44822278 | ||||||
| chr1:44842945 | G | C | 3 | a0001c0010t0002 a0001c0010t0006 a0001c0023t0002 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-13C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/22 | 13 | chr1 | 44842945 | ||||||
| chr1:44842982 | G | A | 1 | a0001c0003t0007 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/22 | 50 | chr1 | 44842982 | ||||||
| chr1:44843154 | C | T | 2 | a0001c0010t0002 a0001c0023t0002 |
3 | HG03098.hp2 NA20129.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-222G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/22 | 222 | chr1 | 44843154 | ||||||
| chr1:44843239 | C | G | 1 | a0001c0001t0003 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-307G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/22 | 307 | chr1 | 44843239 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44822729 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3358-60C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 21/21 | chr1 | 44822729 | |||||||
| chr1:44822809 | G | A | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3358-140C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 21/21 | chr1 | 44822809 | |||||||
| chr1:44822820 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG00639.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3358-151C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 21/21 | chr1 | 44822820 | |||||||
| chr1:44822855 | C | G | 72 | a0001c0003t0001g0006 a0001c0003t0001g0014 a0001c0003t0001g0036 others(69): Show |
89 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.3358-186G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 21/21 | chr1 | 44822855 | |||||||
| chr1:44823547 | T | C | 1 | a0008c0027t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3115-162A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823547 | |||||||
| chr1:44823597 | C | T | 1 | a0001c0021t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3115-212G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823597 | |||||||
| chr1:44823660 | C | T | 1 | a0002c0004t0001g0154 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3115-275G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823660 | |||||||
| chr1:44823667 | G | A | 1 | a0001c0003t0001g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3115-282C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823667 | |||||||
| chr1:44823670 | G | A | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3115-285C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823670 | |||||||
| chr1:44823680 | T | C | 1 | a0001c0003t0001g0192 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3115-295A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823680 | |||||||
| chr1:44823704 | T | C | 139 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0029 others(136): Show |
191 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.3115-319A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823704 | |||||||
| chr1:44823726 | G | A | 3 | a0001c0017t0001g0203 a0002c0006t0001g0159 a0007c0026t0001g0233 |
3 | HG02258.hp2 HG03225.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3115-341C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823726 | |||||||
| chr1:44823737 | C | G | 138 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0029 others(135): Show |
190 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.3115-352G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823737 | |||||||
| chr1:44823914 | G | A | 69 | a0001c0003t0001g0006 a0001c0003t0001g0014 a0001c0003t0001g0036 others(66): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.3115-529C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823914 | |||||||
| chr1:44823936 | T | TCAAA | 24 | a0001c0002t0001g0151 a0001c0002t0001g0212 a0001c0002t0001g0216 others(21): Show |
32 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.3115-555_3115-552d others(6): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823936 | |||||||
| chr1:44823936 | T | TCAAACAA others(5): Show |
2 | a0001c0017t0001g0203 a0007c0026t0001g0233 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3115-563_3115-552d others(14): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823936 | |||||||
| chr1:44823936 | TCAAA | T | 71 | a0001c0001t0001g0122 a0001c0002t0001g0223 a0001c0003t0001g0006 others(68): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.3115-555_3115-552d others(6): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823936 | |||||||
| chr1:44823949 | C | A | 1 | a0002c0004t0001g0185 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3115-564G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44823949 | |||||||
| chr1:44824073 | G | T | 1 | a0007c0026t0001g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3115-688C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824073 | |||||||
| chr1:44824081 | GC | G | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3115-697delG | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824081 | |||||||
| chr1:44824420 | T | A | 63 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0029 others(60): Show |
98 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.3115-1035A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824420 | |||||||
| chr1:44824454 | G | A | 2 | a0002c0004t0001g0165 a0002c0004t0001g0167 |
2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.3115-1069C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824454 | |||||||
| chr1:44824500 | AT | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(161): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3115-1116delA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824500 | |||||||
| chr1:44824660 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3115-1275C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824660 | |||||||
| chr1:44824680 | T | G | 1 | a0001c0002t0001g0044 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3115-1295A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824680 | |||||||
| chr1:44824695 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3115-1310G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824695 | |||||||
| chr1:44824822 | G | C | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3114+1428C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44824822 | |||||||
| chr1:44825122 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0126 |
3 | HG02723.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3114+1128A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825122 | |||||||
| chr1:44825142 | T | A | 1 | a0002c0004t0001g0185 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3114+1108A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825142 | |||||||
| chr1:44825231 | G | A | 3 | a0001c0002t0001g0151 a0001c0002t0001g0212 a0001c0002t0001g0216 |
3 | HG01243.hp2 HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3114+1019C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825231 | |||||||
| chr1:44825431 | C | T | 1 | a0001c0003t0001g0195 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3114+819G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825431 | |||||||
| chr1:44825622 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3114+628C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825622 | |||||||
| chr1:44825683 | C | G | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3114+567G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825683 | |||||||
| chr1:44825743 | T | C | 2 | a0001c0017t0001g0203 a0007c0026t0001g0233 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3114+507A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825743 | |||||||
| chr1:44825769 | C | T | 6 | a0002c0004t0001g0156 a0002c0004t0001g0172 a0002c0004t0001g0185 others(3): Show |
6 | NA18951.hp1 NA18953.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.3114+481G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825769 | |||||||
| chr1:44825844 | C | CT | 78 | a0001c0001t0001g0031 a0001c0001t0001g0104 a0001c0001t0001g0105 others(75): Show |
96 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3114+405dupA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825844 | |||||||
| chr1:44825844 | C | CTT | 23 | a0001c0003t0001g0162 a0001c0003t0001g0169 a0001c0003t0001g0176 others(20): Show |
30 | HG00323.hp2 HG00621.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3114+404_3114+405d others(4): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825844 | |||||||
| chr1:44825844 | CT | C | 7 | a0001c0001t0001g0053 a0001c0001t0001g0085 a0001c0001t0001g0086 others(4): Show |
7 | HG01516.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3114+405delA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825844 | |||||||
| chr1:44825908 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3114+342G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44825908 | |||||||
| chr1:44826004 | C | A | 18 | a0001c0005t0001g0008 a0001c0005t0001g0012 a0001c0005t0001g0032 others(15): Show |
25 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.3114+246G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44826004 | |||||||
| chr1:44826036 | G | T | 24 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0042 others(21): Show |
47 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.3114+214C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44826036 | |||||||
| chr1:44826236 | G | A | 69 | a0001c0003t0001g0006 a0001c0003t0001g0014 a0001c0003t0001g0036 others(66): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.3114+14C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 19/21 | chr1 | 44826236 | |||||||
| chr1:44826811 | C | T | 18 | a0001c0005t0001g0008 a0001c0005t0001g0012 a0001c0005t0001g0032 others(15): Show |
25 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2696-43G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 17/21 | chr1 | 44826811 | |||||||
| chr1:44826894 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02257.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.2695+8T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 17/21 | chr1 | 44826894 | |||||||
| chr1:44827385 | G | A | 18 | a0001c0005t0001g0008 a0001c0005t0001g0012 a0001c0005t0001g0032 others(15): Show |
25 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2371+17C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 15/21 | chr1 | 44827385 | |||||||
| chr1:44828266 | G | A | 1 | a0001c0002t0001g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1709+30C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 13/21 | chr1 | 44828266 | |||||||
| chr1:44828472 | C | T | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1590+34G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 12/21 | chr1 | 44828472 | |||||||
| chr1:44828484 | T | C | 140 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0002t0001g0002 others(137): Show |
192 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1590+22A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 12/21 | chr1 | 44828484 | |||||||
| chr1:44828869 | G | C | 1 | a0001c0021t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1464+113C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 11/21 | chr1 | 44828869 | |||||||
| chr1:44829149 | T | C | 1 | a0001c0017t0001g0203 | 1 | HG02258.hp2 | splice_region_variant&intron_variant | LOW | c.1371+8A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 10/21 | chr1 | 44829149 | |||||||
| chr1:44830239 | G | GTA | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(204): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.814-210_814-209ins others(2): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830239 | |||||||
| chr1:44830296 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.814-266T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830296 | |||||||
| chr1:44830319 | A | G | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.814-289T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830319 | |||||||
| chr1:44830399 | G | A | 1 | a0007c0026t0001g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.814-369C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830399 | |||||||
| chr1:44830584 | A | C | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+264T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830584 | |||||||
| chr1:44830587 | C | CA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0054 others(9): Show |
17 | HG01069.hp1 HG01258.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.813+260dupT | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(3): Show |
10 | a0001c0002t0001g0002 a0001c0002t0001g0042 a0001c0002t0001g0045 others(7): Show |
26 | HG00735.hp2 HG01081.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.813+251_813+260dup others(10): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(4): Show |
10 | a0001c0002t0001g0004 a0001c0002t0001g0213 a0001c0002t0001g0214 others(7): Show |
16 | HG00544.hp1 HG00558.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.813+250_813+260dup others(11): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(5): Show |
1 | a0001c0002t0001g0225 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.813+249_813+260dup others(12): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0001g0232 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.813+248_813+260dup others(13): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(9): Show |
10 | a0002c0004t0001g0034 a0002c0004t0001g0131 a0002c0004t0001g0152 others(7): Show |
11 | HG00621.hp2 HG01123.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.813+245_813+260dup others(16): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(10): Show |
24 | a0001c0003t0001g0038 a0001c0003t0001g0039 a0001c0003t0001g0162 others(21): Show |
30 | HG00323.hp2 HG01099.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.813+244_813+260dup others(17): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(11): Show |
22 | a0001c0003t0001g0006 a0001c0003t0001g0014 a0001c0003t0001g0036 others(19): Show |
30 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.813+260_813+261ins others(18): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(12): Show |
9 | a0001c0003t0001g0040 a0001c0003t0001g0163 a0001c0003t0001g0187 others(6): Show |
10 | HG00280.hp1 HG00408.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.813+260_813+261ins others(19): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(13): Show |
3 | a0001c0003t0001g0161 a0001c0003t0001g0198 a0001c0021t0001g0217 |
3 | HG00423.hp2 HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.813+260_813+261ins others(20): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(14): Show |
3 | a0001c0003t0001g0164 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | HG02486.hp1 NA18944.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.813+260_813+261ins others(21): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(15): Show |
2 | a0001c0002t0001g0151 a0001c0002t0001g0216 |
2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.813+260_813+261ins others(22): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(16): Show |
2 | a0001c0002t0001g0212 a0001c0008t0001g0132 |
2 | HG02145.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.813+260_813+261ins others(23): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(17): Show |
4 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0107 others(1): Show |
6 | HG01167.hp1 HG01943.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+260_813+261ins others(24): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(18): Show |
8 | a0001c0002t0001g0029 a0001c0002t0001g0094 a0001c0002t0001g0125 others(5): Show |
11 | HG01884.hp1 HG02630.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+260_813+261ins others(25): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(19): Show |
9 | a0001c0002t0001g0108 a0001c0002t0001g0115 a0001c0005t0001g0008 others(6): Show |
12 | HG01123.hp2 HG02055.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.813+260_813+261ins others(26): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(20): Show |
4 | a0001c0002t0001g0063 a0001c0002t0001g0109 a0001c0005t0001g0032 others(1): Show |
6 | HG02257.hp1 HG03486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+260_813+261ins others(27): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(21): Show |
2 | a0001c0005t0001g0145 a0006c0015t0001g0144 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+260_813+261ins others(28): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(23): Show |
1 | a0001c0005t0001g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.813+260_813+261ins others(30): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(24): Show |
1 | a0001c0005t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.813+260_813+261ins others(31): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(25): Show |
2 | a0001c0002t0001g0110 a0001c0005t0001g0148 |
2 | HG02886.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.813+260_813+261ins others(32): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | C | CAAAAAAA others(35): Show |
1 | a0001c0005t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.813+260_813+261ins others(42): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830587 | CA | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0067 others(2): Show |
6 | HG01099.hp1 HG03139.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+260delT | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830587 | |||||||
| chr1:44830605 | G | A | 71 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0003t0001g0006 others(68): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.813+243C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830605 | |||||||
| chr1:44830650 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.813+198T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830650 | |||||||
| chr1:44830743 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.813+105C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 6/21 | chr1 | 44830743 | |||||||
| chr1:44831080 | C | T | 72 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0003t0001g0006 others(69): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.618-37G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 5/21 | chr1 | 44831080 | |||||||
| chr1:44831108 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.618-65C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 5/21 | chr1 | 44831108 | |||||||
| chr1:44831445 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.617+261C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 5/21 | chr1 | 44831445 | |||||||
| chr1:44831835 | A | C | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.526-38T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 4/21 | chr1 | 44831835 | |||||||
| chr1:44831911 | C | T | 2 | a0001c0017t0001g0203 a0007c0026t0001g0233 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.525+64G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 4/21 | chr1 | 44831911 | |||||||
| chr1:44832081 | A | C | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-37T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 3/21 | chr1 | 44832081 | |||||||
| chr1:44832081 | A | G | 94 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0157 others(91): Show |
118 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.456-37T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 3/21 | chr1 | 44832081 | |||||||
| chr1:44832112 | C | T | 1 | a0001c0002t0001g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.455+40G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 3/21 | chr1 | 44832112 | |||||||
| chr1:44832386 | G | A | 1 | a0001c0021t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.266-45C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44832386 | |||||||
| chr1:44832554 | G | A | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.266-213C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44832554 | |||||||
| chr1:44832580 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0030 |
4 | HG03490.hp2 HG03492.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-239A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44832580 | |||||||
| chr1:44832682 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.266-341C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44832682 | |||||||
| chr1:44832866 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0112 |
5 | HG00408.hp1 HG02040.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-525C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44832866 | |||||||
| chr1:44833018 | C | T | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.266-677G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833018 | |||||||
| chr1:44833079 | C | T | 3 | a0001c0003t0001g0037 a0001c0003t0001g0039 a0001c0003t0001g0239 |
5 | HG02451.hp1 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-738G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833079 | |||||||
| chr1:44833362 | C | G | 1 | a0001c0010t0006g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.266-1021G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833362 | |||||||
| chr1:44833378 | G | C | 82 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(79): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.266-1037C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833378 | |||||||
| chr1:44833438 | C | CT | 5 | a0001c0001t0001g0026 a0001c0002t0001g0229 a0001c0008t0001g0132 others(2): Show |
6 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-1098dupA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833438 | |||||||
| chr1:44833438 | C | CTT | 74 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(71): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.266-1099_266-1098d others(4): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833438 | |||||||
| chr1:44833602 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.266-1261T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833602 | |||||||
| chr1:44833625 | C | T | 1 | a0003c0018t0004g0081 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.266-1284G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833625 | |||||||
| chr1:44833684 | T | C | 82 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(79): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.266-1343A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833684 | |||||||
| chr1:44833689 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0102 |
2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.266-1348G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833689 | |||||||
| chr1:44833690 | A | G | 82 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(79): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.266-1349T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833690 | |||||||
| chr1:44833707 | G | A | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.266-1366C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833707 | |||||||
| chr1:44833840 | C | T | 79 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(76): Show |
97 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.266-1499G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833840 | |||||||
| chr1:44833972 | C | T | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0029 others(57): Show |
95 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.266-1631G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44833972 | |||||||
| chr1:44834122 | C | CT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
7 | HG00323.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-1782dupA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834122 | |||||||
| chr1:44834122 | C | CTT | 79 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(76): Show |
97 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.266-1783_266-1782d others(4): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834122 | |||||||
| chr1:44834176 | A | G | 73 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(70): Show |
90 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.266-1835T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834176 | |||||||
| chr1:44834276 | C | T | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.266-1935G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834276 | |||||||
| chr1:44834374 | C | T | 82 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0166 others(79): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.266-2033G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834374 | |||||||
| chr1:44834502 | G | A | 2 | a0001c0002t0001g0212 a0001c0002t0001g0216 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.266-2161C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834502 | |||||||
| chr1:44834512 | G | A | 1 | a0001c0021t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.266-2171C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834512 | |||||||
| chr1:44834901 | G | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0029 others(57): Show |
95 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.266-2560C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834901 | |||||||
| chr1:44834902 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.266-2561C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44834902 | |||||||
| chr1:44835185 | T | C | 77 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0181 others(74): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.266-2844A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835185 | |||||||
| chr1:44835243 | G | T | 1 | a0001c0005t0001g0033 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.266-2902C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835243 | |||||||
| chr1:44835277 | G | A | 1 | a0002c0004t0001g0165 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.266-2936C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835277 | |||||||
| chr1:44835434 | A | G | 1 | a0002c0004t0001g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.266-3093T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835434 | |||||||
| chr1:44835441 | T | C | 1 | a0001c0003t0001g0202 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.266-3100A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835441 | |||||||
| chr1:44835504 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.266-3163T>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835504 | |||||||
| chr1:44835568 | C | T | 1 | a0001c0016t0001g0099 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.266-3227G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835568 | |||||||
| chr1:44835619 | G | T | 1 | a0001c0002t0001g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.266-3278C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835619 | |||||||
| chr1:44835667 | C | G | 1 | a0001c0021t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.266-3326G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835667 | |||||||
| chr1:44835783 | G | A | 1 | a0001c0001t0005g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.266-3442C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835783 | |||||||
| chr1:44835884 | G | A | 1 | a0001c0002t0001g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266-3543C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44835884 | |||||||
| chr1:44836063 | G | A | 78 | a0001c0001t0001g0160 a0001c0003t0001g0006 a0001c0003t0001g0014 others(75): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.266-3722C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836063 | |||||||
| chr1:44836117 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.266-3776C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836117 | |||||||
| chr1:44836152 | C | T | 2 | a0001c0002t0001g0045 a0001c0002t0001g0220 |
3 | HG01081.hp2 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.266-3811G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836152 | |||||||
| chr1:44836175 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.266-3834A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836175 | |||||||
| chr1:44836232 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.266-3891C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836232 | |||||||
| chr1:44836358 | C | T | 78 | a0001c0001t0001g0160 a0001c0003t0001g0006 a0001c0003t0001g0014 others(75): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.266-4017G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836358 | |||||||
| chr1:44836382 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.266-4041G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836382 | |||||||
| chr1:44836428 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0130 |
3 | NA18950.hp1 NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.266-4087C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836428 | |||||||
| chr1:44836476 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.266-4135C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836476 | |||||||
| chr1:44836524 | G | A | 4 | a0002c0004t0001g0177 a0002c0004t0001g0178 a0002c0004t0001g0183 others(1): Show |
4 | HG02083.hp1 HG02132.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-4183C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836524 | |||||||
| chr1:44836718 | G | A | 1 | a0001c0008t0001g0132 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.266-4377C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836718 | |||||||
| chr1:44836719 | A | G | 1 | a0001c0008t0001g0132 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.266-4378T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836719 | |||||||
| chr1:44836732 | G | A | 1 | a0001c0008t0001g0132 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.266-4391C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836732 | |||||||
| chr1:44836743 | A | G | 1 | a0007c0026t0001g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.266-4402T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836743 | |||||||
| chr1:44836799 | A | G | 1 | a0001c0005t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.266-4458T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836799 | |||||||
| chr1:44836919 | T | G | 78 | a0001c0001t0001g0160 a0001c0003t0001g0006 a0001c0003t0001g0014 others(75): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.266-4578A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44836919 | |||||||
| chr1:44837121 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0126 |
3 | HG02723.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265+4726G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44837121 | |||||||
| chr1:44837122 | G | A | 69 | a0001c0001t0001g0160 a0001c0003t0001g0006 a0001c0003t0001g0014 others(66): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.265+4725C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44837122 | |||||||
| chr1:44837166 | A | G | 1 | a0001c0003t0001g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.265+4681T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44837166 | |||||||
| chr1:44837340 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+4507G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44837340 | |||||||
| chr1:44837489 | G | A | 1 | a0001c0017t0001g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.265+4358C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44837489 | |||||||
| chr1:44837850 | G | A | 61 | a0001c0001t0001g0221 a0001c0002t0001g0002 a0001c0002t0001g0004 others(58): Show |
96 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.265+3997C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44837850 | |||||||
| chr1:44838015 | G | C | 1 | a0005c0025t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.265+3832C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838015 | |||||||
| chr1:44838034 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.265+3813T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838034 | |||||||
| chr1:44838081 | CA | C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0095 others(6): Show |
9 | NA18522.hp2 NA18942.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+3765delT | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838081 | |||||||
| chr1:44838184 | T | G | 1 | a0001c0002t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.265+3663A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838184 | |||||||
| chr1:44838274 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3573A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838274 | |||||||
| chr1:44838276 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3571A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838276 | |||||||
| chr1:44838278 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3569C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838278 | |||||||
| chr1:44838280 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3567A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838280 | |||||||
| chr1:44838283 | G | A | 1 | a0001c0021t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.265+3564C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838283 | |||||||
| chr1:44838283 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3564C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838283 | |||||||
| chr1:44838284 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3563G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838284 | |||||||
| chr1:44838286 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3561C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838286 | |||||||
| chr1:44838287 | G | A | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+3560C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838287 | |||||||
| chr1:44838287 | G | C | 3 | a0001c0008t0001g0132 a0001c0008t0001g0134 a0001c0008t0001g0135 |
3 | NA18944.hp2 NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.265+3560C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838287 | |||||||
| chr1:44838287 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3560C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838287 | |||||||
| chr1:44838288 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3559G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838288 | |||||||
| chr1:44838290 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3557C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838290 | |||||||
| chr1:44838291 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3556C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838291 | |||||||
| chr1:44838296 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3551G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838296 | |||||||
| chr1:44838298 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3549T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838298 | |||||||
| chr1:44838300 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3547C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838300 | |||||||
| chr1:44838303 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3544C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838303 | |||||||
| chr1:44838305 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3542C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838305 | |||||||
| chr1:44838308 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3539G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838308 | |||||||
| chr1:44838310 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3537G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838310 | |||||||
| chr1:44838318 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3529A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838318 | |||||||
| chr1:44838320 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3527G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838320 | |||||||
| chr1:44838321 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3526T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838321 | |||||||
| chr1:44838323 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3524T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838323 | |||||||
| chr1:44838324 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3523G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838324 | |||||||
| chr1:44838328 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3519C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838328 | |||||||
| chr1:44838329 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3518G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838329 | |||||||
| chr1:44838334 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3513G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838334 | |||||||
| chr1:44838336 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3511C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838336 | |||||||
| chr1:44838337 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3510C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838337 | |||||||
| chr1:44838338 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3509A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838338 | |||||||
| chr1:44838343 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3504C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838343 | |||||||
| chr1:44838344 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3503G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838344 | |||||||
| chr1:44838347 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3500A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838347 | |||||||
| chr1:44838348 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3499A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838348 | |||||||
| chr1:44838350 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3497A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838350 | |||||||
| chr1:44838353 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3494A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838353 | |||||||
| chr1:44838354 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3493C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838354 | |||||||
| chr1:44838357 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3490T>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838357 | |||||||
| chr1:44838363 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3484A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838363 | |||||||
| chr1:44838367 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3480G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838367 | |||||||
| chr1:44838369 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3478C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838369 | |||||||
| chr1:44838370 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3477A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838370 | |||||||
| chr1:44838371 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3476T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838371 | |||||||
| chr1:44838387 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3460T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838387 | |||||||
| chr1:44838390 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3457G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838390 | |||||||
| chr1:44838391 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3456T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838391 | |||||||
| chr1:44838394 | ACCACGCC others(8): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.265+3438_265+3452d others(17): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838394 | |||||||
| chr1:44838493 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.265+3354C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838493 | |||||||
| chr1:44838593 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0095 others(3): Show |
7 | HG00438.hp1 HG00609.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+3254C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838593 | |||||||
| chr1:44838694 | G | A | 2 | a0001c0017t0001g0203 a0007c0026t0001g0233 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.265+3153C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838694 | |||||||
| chr1:44838729 | C | CT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0001g0133 others(4): Show |
7 | HG01361.hp1 NA18944.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+3117dupA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838729 | |||||||
| chr1:44838732 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.265+3115A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838732 | |||||||
| chr1:44838734 | T | C | 76 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0181 others(73): Show |
93 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.265+3113A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838734 | |||||||
| chr1:44838988 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.265+2859G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838988 | |||||||
| chr1:44838989 | G | T | 1 | a0001c0002t0001g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.265+2858C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44838989 | |||||||
| chr1:44839102 | G | A | 69 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0113 others(66): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.265+2745C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839102 | |||||||
| chr1:44839170 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG00438.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.265+2677G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839170 | |||||||
| chr1:44839182 | G | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0114 a0001c0005t0001g0140 others(2): Show |
5 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+2665C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839182 | |||||||
| chr1:44839185 | C | T | 1 | a0001c0016t0001g0099 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.265+2662G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839185 | |||||||
| chr1:44839193 | T | A | 2 | a0001c0001t0001g0077 a0004c0014t0001g0076 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.265+2654A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839193 | |||||||
| chr1:44839287 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
7 | HG00639.hp1 HG01255.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+2560C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839287 | |||||||
| chr1:44839361 | C | CA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(54): Show |
111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.265+2485dupT | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | C | CAAAAA | 11 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0043 others(8): Show |
15 | HG01243.hp2 HG01891.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.265+2481_265+2485d others(7): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | C | CAAAAAA | 17 | a0001c0001t0001g0089 a0001c0001t0001g0219 a0001c0001t0001g0221 others(14): Show |
39 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.265+2480_265+2485d others(8): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | C | CAAAAAAA | 7 | a0001c0002t0001g0047 a0001c0002t0001g0229 a0001c0002t0001g0231 others(4): Show |
8 | HG01516.hp1 HG01517.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.265+2479_265+2485d others(9): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | C | CAAAAAAA others(3): Show |
1 | a0001c0008t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265+2476_265+2485d others(12): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | C | CAAAAAAA others(4): Show |
1 | a0001c0008t0001g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.265+2475_265+2485d others(13): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | CAAAAAAA others(1): Show |
C | 73 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(70): Show |
91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.265+2478_265+2485d others(10): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839361 | CAAAAAAA others(4): Show |
C | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+2475_265+2485d others(13): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839361 | |||||||
| chr1:44839384 | C | A | 1 | a0007c0026t0001g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.265+2463G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839384 | |||||||
| chr1:44839386 | G | A | 1 | a0007c0026t0001g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.265+2461C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839386 | |||||||
| chr1:44839411 | C | T | 1 | a0001c0003t0001g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.265+2436G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839411 | |||||||
| chr1:44839412 | A | C | 1 | a0001c0003t0001g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.265+2435T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839412 | |||||||
| chr1:44839413 | C | A | 1 | a0001c0003t0001g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.265+2434G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839413 | |||||||
| chr1:44839428 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.265+2419C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839428 | |||||||
| chr1:44839438 | G | A | 116 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0157 others(113): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.265+2409C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839438 | |||||||
| chr1:44839645 | T | G | 1 | a0001c0003t0007g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265+2202A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839645 | |||||||
| chr1:44839722 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.265+2125G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839722 | |||||||
| chr1:44839768 | C | T | 4 | a0001c0001t0001g0133 a0001c0008t0001g0132 a0001c0008t0001g0134 others(1): Show |
4 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+2079G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839768 | |||||||
| chr1:44839820 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(65): Show |
124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.265+2027C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839820 | |||||||
| chr1:44839834 | G | A | 73 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(70): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.265+2013C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839834 | |||||||
| chr1:44839835 | G | A | 1 | a0001c0003t0001g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.265+2012C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839835 | |||||||
| chr1:44839900 | C | T | 3 | a0001c0001t0001g0080 a0001c0005t0001g0033 a0001c0005t0001g0136 |
4 | HG01515.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+1947G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44839900 | |||||||
| chr1:44840069 | CAGCCCTC others(12): Show |
C | 3 | a0001c0010t0002g0015 a0001c0010t0006g0241 a0001c0023t0002g0049 |
4 | HG03098.hp2 HG03130.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+1759_265+1777d others(21): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840069 | |||||||
| chr1:44840101 | A | AT | 43 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(40): Show |
57 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.265+1745dupA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840101 | |||||||
| chr1:44840101 | AT | A | 29 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(26): Show |
34 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.265+1745delA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840101 | |||||||
| chr1:44840165 | C | T | 1 | a0001c0017t0001g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.265+1682G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840165 | |||||||
| chr1:44840351 | C | T | 115 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(112): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.265+1496G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840351 | |||||||
| chr1:44840431 | C | G | 1 | a0001c0002t0001g0211 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.265+1416G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840431 | |||||||
| chr1:44840446 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265+1401G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840446 | |||||||
| chr1:44840459 | C | T | 1 | a0002c0006t0001g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.265+1388G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840459 | |||||||
| chr1:44840562 | T | A | 1 | a0001c0002t0001g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.265+1285A>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840562 | |||||||
| chr1:44840580 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.265+1267C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840580 | |||||||
| chr1:44840622 | A | T | 4 | a0001c0001t0001g0133 a0001c0008t0001g0132 a0001c0008t0001g0134 others(1): Show |
4 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1225T>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840622 | |||||||
| chr1:44840659 | C | T | 4 | a0001c0001t0001g0133 a0001c0008t0001g0132 a0001c0008t0001g0134 others(1): Show |
4 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1188G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840659 | |||||||
| chr1:44840723 | CAAAA | C | 4 | a0001c0001t0001g0133 a0001c0008t0001g0132 a0001c0008t0001g0134 others(1): Show |
4 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1120_265+1123d others(6): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840723 | |||||||
| chr1:44840771 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.265+1076C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840771 | |||||||
| chr1:44840923 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0065 others(4): Show |
12 | HG00642.hp1 HG00738.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.265+924C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44840923 | |||||||
| chr1:44841028 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.265+819C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841028 | |||||||
| chr1:44841031 | T | G | 1 | a0001c0002t0001g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.265+816A>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841031 | |||||||
| chr1:44841194 | A | AC | 47 | a0001c0001t0001g0071 a0001c0001t0001g0133 a0001c0001t0001g0219 others(44): Show |
75 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.265+652dupG | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841194 | |||||||
| chr1:44841194 | A | ACC | 25 | a0001c0003t0001g0006 a0001c0003t0001g0039 a0001c0003t0001g0040 others(22): Show |
31 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.265+651_265+652dup others(2): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841194 | |||||||
| chr1:44841194 | A | ACCC | 35 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0179 others(32): Show |
43 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+650_265+652dup others(3): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841194 | |||||||
| chr1:44841194 | A | ACCCC | 12 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(9): Show |
16 | HG00621.hp2 HG01099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.265+649_265+652dup others(4): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841194 | |||||||
| chr1:44841203 | A | C | 70 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(67): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.265+644T>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841203 | |||||||
| chr1:44841212 | C | A | 1 | a0001c0003t0001g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.265+635G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841212 | |||||||
| chr1:44841249 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.265+598T>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841249 | |||||||
| chr1:44841275 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.265+572G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841275 | |||||||
| chr1:44841356 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.265+491G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841356 | |||||||
| chr1:44841709 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+138G>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841709 | |||||||
| chr1:44841788 | C | G | 1 | a0001c0002t0001g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.265+59G>C | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841788 | |||||||
| chr1:44841834 | G | A | 115 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(112): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.265+13C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 2/21 | chr1 | 44841834 | |||||||
| chr1:44842134 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.73-95A>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842134 | |||||||
| chr1:44842226 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.73-187C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842226 | |||||||
| chr1:44842274 | C | CT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0051 others(16): Show |
21 | HG00621.hp1 HG01109.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.73-236dupA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842274 | |||||||
| chr1:44842274 | CT | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(5): Show |
8 | HG02965.hp1 HG03041.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-236delA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842274 | |||||||
| chr1:44842274 | CTT | C | 18 | a0001c0001t0001g0129 a0001c0005t0001g0008 a0001c0005t0001g0012 others(15): Show |
25 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.73-237_73-236delAA | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842274 | |||||||
| chr1:44842274 | CTTTTTTT others(4): Show |
C | 1 | a0002c0006t0001g0150 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.73-246_73-236delAA others(9): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842274 | |||||||
| chr1:44842274 | CTTTTTTT others(5): Show |
C | 112 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0158 others(109): Show |
158 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.73-247_73-236delAA others(10): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842274 | |||||||
| chr1:44842274 | CTTTTTTT others(6): Show |
C | 2 | a0001c0003t0001g0237 a0002c0004t0001g0236 |
2 | NA18968.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.73-248_73-236delAA others(11): Show |
PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842274 | |||||||
| chr1:44842437 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.73-398C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842437 | |||||||
| chr1:44842569 | G | T | 1 | a0002c0004t0001g0131 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.72+292C>A | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842569 | |||||||
| chr1:44842574 | G | C | 1 | a0002c0004t0001g0238 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.72+287C>G | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842574 | |||||||
| chr1:44842737 | G | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0157 others(134): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.72+124C>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842737 | |||||||
| chr1:44842757 | C | A | 1 | a0001c0003t0001g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.72+104G>T | PTCH2 | ENSG00000117425.14 | transcript | ENST00000372192.4 | protein_coding | 1/21 | chr1 | 44842757 |