Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56134 |
| ensemblid | ENSG00000243232.6 |
| hgncid | 8677 |
| symbol | PCDHAC2 |
| name | protocadherin alpha subfamily C, 2 |
| refseq_nuc | NM_018899.6 |
| refseq_prot | NP_061722.1 |
| ensembl_nuc | ENST00000289269.7 |
| ensembl_prot | ENSP00000289269.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 140966476 |
| end | 141012347 |
| strand | + |
| ver | v1.2 |
| region | chr5:140966476-141012347 |
| region5000 | chr5:140961476-141017347 |
| regionname0 | PCDHAC2_chr5_140966476_141012347 |
| regionname5000 | PCDHAC2_chr5_140961476_141017347 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1007 | 311 | 77 | 57 | 128 | 14 | 33 | 90 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | MEQAG others(1002): Show |
chr5 | 140961476 | 141017347 |
| a0002 | 0/0 | 1005 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | MEQAG others(1000): Show |
chr5 | 140961476 | 141017347 |
| a0003 | 0/0 | 1007 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | MEQAG others(1002): Show |
chr5 | 140961476 | 141017347 |
| a0004 | 0/0 | 1007 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | MEQAG others(1002): Show |
chr5 | 140961476 | 141017347 |
| a0005 | 0/0 | 1007 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | MEQAG others(1002): Show |
chr5 | 140961476 | 141017347 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3021 | 126 | 22 | 19 | 57 | 10 | 17 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0002 | 0/1 | 3021 | 119 | 28 | 19 | 57 | 2 | 12 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0003 | 0/0 | 3021 | 33 | 15 | 6 | 9 | 2 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0004 | 0/0 | 3021 | 19 | 4 | 10 | 3 | 0 | 2 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0005 | 0/0 | 3021 | 5 | 5 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0009 | 0/0 | 3021 | 2 | 0 | 2 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0013 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0014 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0015 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0016 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0017 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0019 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0001c0020 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0002c0006 | 0/0 | 3015 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3010): Show |
chr5 | 140961476 | 141017347 | ||
| a0002c0007 | 0/0 | 3015 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3010): Show |
chr5 | 140961476 | 141017347 | ||
| a0002c0008 | 0/0 | 3015 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3010): Show |
chr5 | 140961476 | 141017347 | ||
| a0002c0010 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3010): Show |
chr5 | 140961476 | 141017347 | ||
| a0003c0018 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0004c0012 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 | ||
| a0005c0011 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | ATGGA others(3016): Show |
chr5 | 140961476 | 141017347 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5725 | 100 | 20 | 16 | 38 | 10 | 15 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0001t0002 | 0/0 | 5725 | 13 | 0 | 1 | 11 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0001t0004 | 0/0 | 5725 | 8 | 0 | 0 | 8 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0001t0006 | 0/0 | 5725 | 2 | 2 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0001t0009 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0001t0020 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0001t0021 | 0/0 | 5725 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0001 | 0/1 | 5725 | 87 | 9 | 16 | 49 | 0 | 12 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0002 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0003 | 0/0 | 5721 | 9 | 9 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5716): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0004 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0005 | 0/0 | 5725 | 6 | 3 | 3 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0008 | 0/0 | 5725 | 3 | 0 | 0 | 3 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0010 | 0/0 | 5725 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0011 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0012 | 0/0 | 5725 | 2 | 2 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0013 | 0/0 | 5725 | 2 | 0 | 0 | 0 | 2 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0015 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0016 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0017 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0002t0018 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0003t0001 | 0/0 | 5725 | 27 | 12 | 4 | 8 | 2 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0003t0002 | 0/0 | 5725 | 2 | 1 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0003t0003 | 0/0 | 5721 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5716): Show |
chr5 | 140961476 | 141017347 |
| a0001c0003t0009 | 0/0 | 5725 | 2 | 0 | 2 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0003t0019 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0004t0001 | 0/0 | 5725 | 18 | 3 | 10 | 3 | 0 | 2 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0004t0002 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0005t0007 | 0/0 | 5725 | 4 | 4 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0005t0014 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0009t0001 | 0/0 | 5725 | 2 | 0 | 2 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0013t0001 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0014t0002 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0015t0001 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0016t0001 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0017t0001 | 0/0 | 5725 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0019t0011 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0001c0020t0001 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0002c0006t0006 | 0/0 | 5719 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5714): Show |
chr5 | 140961476 | 141017347 |
| a0002c0007t0001 | 0/0 | 5719 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5714): Show |
chr5 | 140961476 | 141017347 |
| a0002c0008t0001 | 0/0 | 5719 | 3 | 3 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5714): Show |
chr5 | 140961476 | 141017347 |
| a0002c0010t0001 | 0/0 | 5719 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5714): Show |
chr5 | 140961476 | 141017347 |
| a0003c0018t0001 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| a0004c0012t0003 | 0/0 | 5721 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5716): Show |
chr5 | 140961476 | 141017347 |
| a0005c0011t0001 | 0/0 | 5725 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | CTTTT others(5720): Show |
chr5 | 140961476 | 141017347 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0020g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0001t0021g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0005 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0013g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0013g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0017g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0002t0018g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0009g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0009g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0003t0019g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0004t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0005t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0005t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0005t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0005t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0005t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0009t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0009t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0013t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0014t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0015t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0016t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0017t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0019t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0001c0020t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0006t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0006t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0006t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0007t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0008t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0008t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0002c0010t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0003c0018t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0004c0012t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| a0005c0011t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0274 | EUR | FIN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | FIN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0164 | EUR | FIN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0035 | EAS | CHS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0287 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0192 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0191 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01081 | hp2 | a0001 | c0020 | t0001 | g0077 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0027 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0172 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0028 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01168 | hp2 | a0001 | c0009 | t0001 | g0200 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01169 | hp2 | a0001 | c0009 | t0001 | g0199 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01175 | hp2 | a0001 | c0001 | t0020 | g0065 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0288 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01256 | hp2 | a0001 | c0003 | t0009 | g0271 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01258 | hp2 | a0001 | c0003 | t0009 | g0272 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0030 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01346 | hp1 | a0003 | c0018 | t0001 | g0031 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0008 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0029 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01516 | hp1 | a0001 | c0002 | t0013 | g0183 | EUR | IBS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01517 | hp2 | a0001 | c0002 | t0013 | g0014 | EUR | IBS | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01884 | hp1 | a0001 | c0014 | t0002 | g0170 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01884 | hp2 | a0002 | c0007 | t0001 | g0006 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0058 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01934 | hp1 | a0001 | c0002 | t0005 | g0182 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01934 | hp2 | a0001 | c0001 | t0009 | g0008 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01978 | hp2 | a0001 | c0004 | t0001 | g0297 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0202 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02027 | hp1 | a0001 | c0004 | t0001 | g0291 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02055 | hp1 | a0001 | c0003 | t0019 | g0282 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0057 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | CDX | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | CDX | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | CDX | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0248 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0277 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0294 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02630 | hp2 | a0004 | c0012 | t0003 | g0122 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02683 | hp2 | a0001 | c0017 | t0001 | g0101 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0081 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02738 | hp2 | a0001 | c0001 | t0021 | g0132 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0019 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0059 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02818 | hp1 | a0001 | c0002 | t0016 | g0264 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02818 | hp2 | a0001 | c0002 | t0005 | g0194 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02896 | hp2 | a0001 | c0005 | t0007 | g0044 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02897 | hp2 | a0001 | c0005 | t0007 | g0043 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02922 | hp2 | a0002 | c0010 | t0001 | g0121 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0275 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02965 | hp2 | a0002 | c0006 | t0006 | g0022 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02970 | hp1 | a0001 | c0005 | t0007 | g0042 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0055 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0032 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03130 | hp1 | a0002 | c0006 | t0006 | g0020 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03130 | hp2 | a0001 | c0002 | t0011 | g0269 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0048 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03195 | hp2 | a0001 | c0005 | t0014 | g0025 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03209 | hp1 | a0001 | c0002 | t0012 | g0054 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03209 | hp2 | a0001 | c0002 | t0010 | g0250 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0190 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03453 | hp1 | a0001 | c0002 | t0010 | g0249 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0189 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0068 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03516 | hp2 | a0001 | c0004 | t0002 | g0286 | AFR | ESN | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0253 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03540 | hp2 | a0002 | c0007 | t0001 | g0023 | AFR | GWD | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0270 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03710 | hp2 | a0005 | c0011 | t0001 | g0209 | SAS | PJL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0296 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0171 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0221 | SAS | STU | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | STU | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | YRI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0069 | AFR | YRI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | CHB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | CHB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18906 | hp1 | a0002 | c0008 | t0001 | g0168 | AFR | YRI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | YRI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18941 | hp2 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18957 | hp2 | a0001 | c0002 | t0008 | g0126 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18991 | hp2 | a0001 | c0002 | t0017 | g0232 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18995 | hp1 | a0001 | c0016 | t0001 | g0142 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18995 | hp2 | a0001 | c0002 | t0008 | g0098 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19001 | hp1 | a0001 | c0002 | t0008 | g0049 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19005 | hp1 | a0001 | c0004 | t0001 | g0290 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19011 | hp1 | a0001 | c0015 | t0001 | g0105 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | LWK | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19030 | hp2 | a0002 | c0008 | t0001 | g0273 | AFR | LWK | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19043 | hp1 | a0001 | c0005 | t0007 | g0268 | AFR | LWK | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19057 | hp1 | a0001 | c0002 | t0015 | g0197 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0292 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19068 | hp1 | a0001 | c0002 | t0018 | g0241 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0193 | AFR | YRI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA19240 | hp2 | a0002 | c0008 | t0001 | g0260 | AFR | YRI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA20129 | hp2 | a0001 | c0013 | t0001 | g0112 | AFR | ASW | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0293 | SAS | GIH | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02109 | hp2 | a0002 | c0006 | t0006 | g0021 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02486 | hp1 | a0002 | c0007 | t0001 | g0006 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0060 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG02559 | hp2 | a0001 | c0019 | t0011 | g0067 | AFR | ACB | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0276 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0056 | AFR | MSL | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | USA | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | USA | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0153 | REF | REF | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0143 | REF | REF | PCDHAC2_chr5_140961476_141017347 | PCDHAC2 | chr5 | 140961476 | 141017347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:140966860 | TTGCTGC | T | 1 | a0002 | 10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
disruptive_inframe_deletion | MODERATE | c.102_107delGCTGCT | p.Leu35_Leu36del | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 393/5725 | 102/3024 | 34/1007 | INFO_REALIGN_3_PRIME | chr5 | 140966860 | ||
| chr5:140967997 | C | G | 1 | a0004 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1231C>G | p.Arg411Gly | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 1522/5725 | 1231/3024 | 411/1007 | chr5 | 140967997 | |||
| chr5:140982540 | C | G | 1 | a0005 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2690C>G | p.Pro897Arg | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/4 | 2981/5725 | 2690/3024 | 897/1007 | chr5 | 140982540 | |||
| chr5:140982557 | A | G | 1 | a0003 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2707A>G | p.Thr903Ala | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/4 | 2998/5725 | 2707/3024 | 903/1007 | chr5 | 140982557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:140966883 | T | A | 13 | a0001c0002 a0001c0003 a0001c0004 others(10): Show |
191 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(188): Show |
synonymous_variant | LOW | c.117T>A | p.Pro39Pro | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 408/5725 | 117/3024 | 39/1007 | chr5 | 140966883 | |||
| chr5:140967085 | C | A | 1 | a0002c0006 | 3 | HG02109.hp2 HG02965.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.319C>A | p.Arg107Arg | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 610/5725 | 319/3024 | 107/1007 | chr5 | 140967085 | |||
| chr5:140967127 | T | C | 4 | a0001c0002 a0001c0009 a0004c0012 others(1): Show |
122 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
synonymous_variant | LOW | c.361T>C | p.Leu121Leu | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 652/5725 | 361/3024 | 121/1007 | chr5 | 140967127 | |||
| chr5:140967255 | T | C | 1 | a0001c0015 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.489T>C | p.Pro163Pro | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 780/5725 | 489/3024 | 163/1007 | chr5 | 140967255 | |||
| chr5:140967411 | A | T | 1 | a0001c0014 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.645A>T | p.Leu215Leu | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 936/5725 | 645/3024 | 215/1007 | chr5 | 140967411 | |||
| chr5:140967468 | C | T | 4 | a0001c0002 a0001c0009 a0004c0012 others(1): Show |
122 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
synonymous_variant | LOW | c.702C>T | p.Ile234Ile | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 993/5725 | 702/3024 | 234/1007 | chr5 | 140967468 | |||
| chr5:140967813 | C | T | 1 | a0001c0004 | 19 | HG00738.hp2 HG01099.hp2 HG01106.hp2 others(16): Show |
synonymous_variant | LOW | c.1047C>T | p.Cys349Cys | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 1338/5725 | 1047/3024 | 349/1007 | chr5 | 140967813 | |||
| chr5:140967846 | C | T | 1 | a0001c0009 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1080C>T | p.Asp360Asp | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 1371/5725 | 1080/3024 | 360/1007 | chr5 | 140967846 | |||
| chr5:140968287 | C | T | 1 | a0001c0005 | 5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.1521C>T | p.Ser507Ser | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 1812/5725 | 1521/3024 | 507/1007 | chr5 | 140968287 | |||
| chr5:140968317 | A | T | 1 | a0001c0020 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.1551A>T | p.Pro517Pro | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 1842/5725 | 1551/3024 | 517/1007 | chr5 | 140968317 | |||
| chr5:140968329 | T | C | 1 | a0001c0016 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.1563T>C | p.Tyr521Tyr | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 1854/5725 | 1563/3024 | 521/1007 | chr5 | 140968329 | |||
| chr5:140968743 | C | T | 1 | a0001c0019 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1977C>T | p.Thr659Thr | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 2268/5725 | 1977/3024 | 659/1007 | chr5 | 140968743 | |||
| chr5:140968974 | G | A | 4 | a0001c0005 a0001c0013 a0002c0007 others(1): Show |
10 | HG01884.hp2 HG02486.hp1 HG02896.hp2 others(7): Show |
synonymous_variant | LOW | c.2208G>A | p.Ala736Ala | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 2499/5725 | 2208/3024 | 736/1007 | chr5 | 140968974 | |||
| chr5:140969226 | G | A | 1 | a0002c0007 | 3 | HG01884.hp2 HG02486.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.2460G>A | p.Ser820Ser | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 2751/5725 | 2460/3024 | 820/1007 | chr5 | 140969226 | |||
| chr5:141009664 | G | C | 1 | a0001c0017 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.2751G>C | p.Ala917Ala | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 3042/5725 | 2751/3024 | 917/1007 | chr5 | 141009664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:140966505 | A | C | 1 | a0001c0002t0013 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-262A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 262 | chr5 | 140966505 | ||||||
| chr5:140966543 | A | G | 2 | a0001c0002t0010 a0001c0002t0012 |
5 | HG02258.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-224A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | 224 | chr5 | 140966543 | ||||||
| chr5:140966638 | T | G | 2 | a0001c0005t0007 a0001c0005t0014 |
5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-129T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/4 | chr5 | 140966638 | |||||||
| chr5:141009948 | T | A | 1 | a0001c0002t0015 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 11 | chr5 | 141009948 | ||||||
| chr5:141009951 | A | G | 2 | a0001c0001t0004 a0001c0002t0004 |
9 | HG00423.hp1 HG02135.hp1 NA18941.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*14A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 14 | chr5 | 141009951 | ||||||
| chr5:141010220 | C | T | 2 | a0001c0001t0006 a0002c0006t0006 |
5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*283C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 283 | chr5 | 141010220 | ||||||
| chr5:141010368 | C | G | 1 | a0001c0001t0021 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*431C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 431 | chr5 | 141010368 | ||||||
| chr5:141010530 | A | T | 1 | a0001c0001t0020 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 593 | chr5 | 141010530 | ||||||
| chr5:141010893 | A | G | 2 | a0001c0001t0009 a0001c0003t0009 |
3 | HG01256.hp2 HG01258.hp2 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*956A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 956 | chr5 | 141010893 | ||||||
| chr5:141011016 | A | G | 1 | a0001c0002t0008 | 3 | NA18957.hp2 NA18995.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1079A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1079 | chr5 | 141011016 | ||||||
| chr5:141011336 | T | C | 1 | a0001c0002t0005 | 6 | HG01069.hp1 HG01071.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1399T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1399 | chr5 | 141011336 | ||||||
| chr5:141011337 | G | T | 6 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0011 others(3): Show |
16 | HG01891.hp1 HG02055.hp2 HG02258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1400G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1400 | chr5 | 141011337 | ||||||
| chr5:141011606 | A | G | 2 | a0001c0003t0019 a0001c0005t0014 |
2 | HG02055.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1669A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1669 | chr5 | 141011606 | ||||||
| chr5:141011890 | A | G | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0008 others(3): Show |
21 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1953A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1953 | chr5 | 141011890 | ||||||
| chr5:141011896 | T | A | 1 | a0001c0002t0016 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1959 | chr5 | 141011896 | ||||||
| chr5:141011897 | CTATT | C | 3 | a0001c0002t0003 a0001c0003t0003 a0004c0012t0003 |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1963_*1966delTTTA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 1963 | INFO_REALIGN_3_PRIME | chr5 | 141011897 | |||||
| chr5:141012224 | C | T | 1 | a0001c0002t0018 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2287C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 2287 | chr5 | 141012224 | ||||||
| chr5:141012340 | G | A | 1 | a0001c0002t0017 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 4/4 | 2403 | chr5 | 141012340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:140969579 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2565+248G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140969579 | |||||||
| chr5:140969974 | A | G | 3 | a0001c0001t0001g0295 a0001c0004t0001g0296 a0001c0004t0001g0297 |
3 | HG01978.hp2 HG03834.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.2565+643A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140969974 | |||||||
| chr5:140970255 | A | G | 12 | a0001c0001t0001g0285 a0001c0001t0001g0289 a0001c0002t0001g0293 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2565+924A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970255 | |||||||
| chr5:140970314 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2565+983A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970314 | |||||||
| chr5:140970316 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2565+985A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970316 | |||||||
| chr5:140970370 | C | T | 2 | a0001c0001t0006g0279 a0001c0001t0006g0280 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2565+1039C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970370 | |||||||
| chr5:140970537 | GT | G | 9 | a0001c0003t0001g0007 a0001c0003t0001g0019 a0001c0003t0001g0024 others(6): Show |
11 | HG01496.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2565+1209delT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140970537 | ||||||
| chr5:140970554 | G | A | 7 | a0001c0001t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.2565+1223G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970554 | |||||||
| chr5:140970854 | T | TC | 24 | a0001c0001t0001g0026 a0001c0001t0006g0279 a0001c0001t0006g0280 others(21): Show |
26 | HG00280.hp1 HG01099.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2565+1525dupC | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140970854 | ||||||
| chr5:140970956 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
7 | HG00609.hp1 HG00673.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.2565+1625G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970956 | |||||||
| chr5:140970960 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0205 a0001c0001t0001g0220 others(101): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2565+1629G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140970960 | |||||||
| chr5:140971075 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2565+1744T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140971075 | |||||||
| chr5:140971294 | T | C | 1 | a0001c0002t0001g0010 | 2 | NA19084.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2565+1963T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140971294 | |||||||
| chr5:140971359 | G | T | 2 | a0001c0003t0009g0271 a0001c0003t0009g0272 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2565+2028G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140971359 | |||||||
| chr5:140971488 | A | C | 15 | a0001c0001t0001g0026 a0001c0001t0006g0279 a0001c0001t0006g0280 others(12): Show |
15 | HG00280.hp1 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2565+2157A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140971488 | |||||||
| chr5:140971527 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(2): Show |
6 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2565+2196A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140971527 | |||||||
| chr5:140971689 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2565+2358T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140971689 | |||||||
| chr5:140971749 | CAT | C | 7 | a0001c0001t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.2565+2421_2565+242 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140971749 | ||||||
| chr5:140972101 | A | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0177 a0001c0001t0001g0181 others(15): Show |
19 | HG00323.hp1 HG00621.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2565+2770A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972101 | |||||||
| chr5:140972218 | C | A | 1 | a0001c0014t0002g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2565+2887C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972218 | |||||||
| chr5:140972260 | C | T | 2 | a0001c0002t0001g0293 a0001c0004t0001g0294 |
2 | HG02293.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2565+2929C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972260 | |||||||
| chr5:140972262 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2565+2931C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972262 | |||||||
| chr5:140972406 | A | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(5): Show |
9 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2565+3075A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972406 | |||||||
| chr5:140972660 | AT | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0039 others(116): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.2565+3351delT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140972660 | ||||||
| chr5:140972660 | ATT | A | 17 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0001g0011 others(14): Show |
18 | HG01069.hp2 HG01167.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.2565+3350_2565+335 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140972660 | ||||||
| chr5:140972728 | A | G | 3 | a0001c0002t0010g0248 a0001c0002t0010g0249 a0001c0002t0010g0250 |
3 | HG02258.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2565+3397A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972728 | |||||||
| chr5:140972729 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2565+3398T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972729 | |||||||
| chr5:140972749 | C | T | 6 | a0001c0003t0001g0007 a0001c0003t0001g0024 a0001c0005t0007g0268 others(3): Show |
8 | HG01496.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2565+3418C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972749 | |||||||
| chr5:140972813 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2565+3482G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972813 | |||||||
| chr5:140972838 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | NA18962.hp1 NA19005.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.2565+3507A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140972838 | |||||||
| chr5:140973042 | T | C | 2 | a0001c0014t0002g0170 a0002c0008t0001g0273 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2565+3711T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973042 | |||||||
| chr5:140973052 | G | C | 4 | a0001c0002t0011g0269 a0001c0003t0002g0270 a0001c0003t0019g0282 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+3721G>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973052 | |||||||
| chr5:140973078 | C | T | 18 | a0001c0001t0001g0177 a0001c0002t0010g0248 a0001c0002t0010g0249 others(15): Show |
18 | HG00621.hp2 HG01106.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2565+3747C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973078 | |||||||
| chr5:140973199 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2565+3868G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973199 | |||||||
| chr5:140973210 | C | T | 10 | a0001c0003t0001g0007 a0001c0003t0001g0024 a0001c0003t0001g0275 others(7): Show |
12 | HG01496.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2565+3879C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973210 | |||||||
| chr5:140973293 | A | G | 5 | a0001c0001t0001g0247 a0001c0001t0001g0295 a0001c0002t0001g0188 others(2): Show |
5 | HG02015.hp1 NA18947.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+3962A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973293 | |||||||
| chr5:140973582 | T | C | 1 | a0001c0002t0012g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2565+4251T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140973582 | |||||||
| chr5:140974189 | G | T | 1 | a0001c0003t0001g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2566-4760G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974189 | |||||||
| chr5:140974221 | T | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG01515.hp2 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2566-4728T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974221 | |||||||
| chr5:140974322 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0004t0001g0027 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.2566-4627G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974322 | |||||||
| chr5:140974355 | C | T | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2566-4594C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974355 | |||||||
| chr5:140974459 | C | G | 4 | a0001c0002t0011g0269 a0001c0003t0002g0270 a0001c0003t0019g0282 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-4490C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974459 | |||||||
| chr5:140974586 | A | G | 1 | a0002c0008t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2566-4363A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974586 | |||||||
| chr5:140974672 | T | G | 1 | a0001c0002t0012g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2566-4277T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140974672 | |||||||
| chr5:140975044 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0001t0001g0078 others(4): Show |
7 | HG01081.hp2 HG01515.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2566-3905G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140975044 | |||||||
| chr5:140975154 | G | C | 6 | a0001c0002t0005g0182 a0001c0002t0005g0190 a0001c0002t0005g0191 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2566-3795G>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140975154 | |||||||
| chr5:140975505 | A | G | 1 | a0001c0002t0001g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2566-3444A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140975505 | |||||||
| chr5:140975809 | TA | T | 16 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0150 others(13): Show |
16 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.2566-3138delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140975809 | ||||||
| chr5:140975868 | C | T | 1 | a0001c0002t0001g0242 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2566-3081C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140975868 | |||||||
| chr5:140976267 | T | C | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2566-2682T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140976267 | |||||||
| chr5:140976476 | G | A | 1 | a0002c0006t0006g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2566-2473G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140976476 | |||||||
| chr5:140976832 | A | G | 12 | a0001c0001t0001g0289 a0001c0002t0001g0267 a0001c0002t0001g0293 others(9): Show |
12 | HG00280.hp1 HG00738.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2566-2117A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140976832 | |||||||
| chr5:140976924 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2566-2025T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140976924 | |||||||
| chr5:140976952 | C | T | 3 | a0001c0002t0003g0068 a0001c0002t0003g0069 a0001c0002t0003g0070 |
3 | HG02622.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2566-1997C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140976952 | |||||||
| chr5:140977093 | T | C | 1 | a0001c0001t0002g0033 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2566-1856T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977093 | |||||||
| chr5:140977158 | A | G | 1 | a0001c0002t0005g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2566-1791A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977158 | |||||||
| chr5:140977177 | T | G | 3 | a0001c0003t0001g0012 a0001c0003t0001g0019 a0001c0003t0001g0195 |
4 | HG01099.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-1772T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977177 | |||||||
| chr5:140977345 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0083 |
2 | NA18951.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2566-1604T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977345 | |||||||
| chr5:140977429 | C | T | 1 | a0001c0002t0001g0188 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2566-1520C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977429 | |||||||
| chr5:140977482 | A | G | 2 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2566-1467A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977482 | |||||||
| chr5:140977958 | C | T | 18 | a0001c0001t0001g0177 a0001c0002t0010g0248 a0001c0002t0010g0249 others(15): Show |
18 | HG00621.hp2 HG01106.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2566-991C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977958 | |||||||
| chr5:140977966 | G | A | 1 | a0001c0003t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2566-983G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140977966 | |||||||
| chr5:140978370 | A | G | 4 | a0001c0002t0001g0238 a0001c0002t0001g0239 a0001c0002t0001g0240 others(1): Show |
4 | HG02135.hp2 NA18949.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-579A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978370 | |||||||
| chr5:140978652 | C | T | 1 | a0001c0019t0011g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2566-297C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978652 | |||||||
| chr5:140978668 | C | T | 1 | a0001c0001t0004g0066 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2566-281C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978668 | |||||||
| chr5:140978698 | A | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG03710.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2566-251A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978698 | |||||||
| chr5:140978703 | G | C | 1 | a0001c0001t0004g0084 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2566-246G>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978703 | |||||||
| chr5:140978781 | A | C | 12 | a0001c0001t0001g0177 a0001c0002t0010g0248 a0001c0002t0010g0249 others(9): Show |
12 | HG00621.hp2 HG01106.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.2566-168A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978781 | |||||||
| chr5:140978838 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2566-111A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | chr5 | 140978838 | |||||||
| chr5:140978839 | C | CT | 20 | a0001c0001t0001g0177 a0001c0001t0020g0065 a0001c0002t0010g0248 others(17): Show |
20 | HG00621.hp2 HG01106.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.2566-104dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | 140978839 | ||||||
| chr5:140979220 | C | T | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2624+213C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140979220 | |||||||
| chr5:140979350 | A | T | 14 | a0001c0001t0001g0177 a0001c0001t0020g0065 a0001c0003t0001g0173 others(11): Show |
14 | HG00621.hp2 HG01106.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.2624+343A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140979350 | |||||||
| chr5:140979502 | C | T | 5 | a0001c0001t0001g0236 a0001c0002t0001g0016 a0001c0002t0001g0187 others(2): Show |
6 | HG02071.hp2 HG02074.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624+495C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140979502 | |||||||
| chr5:140979514 | C | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
6 | NA18947.hp1 NA18952.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624+507C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140979514 | |||||||
| chr5:140979537 | A | G | 1 | a0001c0003t0001g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2624+530A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140979537 | |||||||
| chr5:140979705 | G | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624+698G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140979705 | |||||||
| chr5:140980164 | G | A | 2 | a0001c0001t0020g0065 a0001c0019t0011g0067 |
2 | HG01175.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2624+1157G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980164 | |||||||
| chr5:140980357 | C | T | 2 | a0001c0001t0020g0065 a0001c0019t0011g0067 |
2 | HG01175.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2624+1350C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980357 | |||||||
| chr5:140980458 | T | C | 1 | a0001c0003t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2624+1451T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980458 | |||||||
| chr5:140980488 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2624+1481G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980488 | |||||||
| chr5:140980560 | G | T | 1 | a0001c0003t0001g0179 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2624+1553G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980560 | |||||||
| chr5:140980684 | G | GA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
7 | HG00323.hp1 HG01175.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2624+1687dupA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 140980684 | ||||||
| chr5:140980712 | T | G | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2624+1705T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980712 | |||||||
| chr5:140980862 | G | A | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2625-1613G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140980862 | |||||||
| chr5:140981034 | A | G | 2 | a0001c0003t0002g0270 a0001c0014t0002g0170 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2625-1441A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981034 | |||||||
| chr5:140981041 | A | C | 6 | a0001c0001t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(3): Show |
6 | HG01099.hp2 HG01168.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.2625-1434A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981041 | |||||||
| chr5:140981487 | T | C | 3 | a0001c0003t0002g0270 a0001c0014t0002g0170 a0002c0008t0001g0273 |
3 | HG01884.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2625-988T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981487 | |||||||
| chr5:140981520 | G | C | 1 | a0001c0002t0001g0251 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2625-955G>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981520 | |||||||
| chr5:140981687 | A | ATCAT | 5 | a0001c0001t0020g0065 a0001c0005t0007g0268 a0001c0019t0011g0067 others(2): Show |
6 | HG01175.hp2 HG01884.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2625-763_2625-760d others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 140981687 | ||||||
| chr5:140981687 | A | ATCATTCA others(1): Show |
2 | a0001c0003t0001g0007 a0001c0003t0001g0024 |
3 | HG01496.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2625-767_2625-760d others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 140981687 | ||||||
| chr5:140981687 | ATCATTCA others(5): Show |
A | 9 | a0001c0001t0001g0177 a0001c0003t0001g0173 a0001c0003t0001g0174 others(6): Show |
9 | HG00621.hp2 HG01106.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2625-771_2625-760d others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | 140981687 | ||||||
| chr5:140981745 | T | C | 4 | a0001c0001t0001g0090 a0001c0002t0001g0196 a0001c0002t0001g0251 others(1): Show |
4 | NA18952.hp1 NA19057.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2625-730T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981745 | |||||||
| chr5:140981860 | A | C | 2 | a0001c0003t0002g0270 a0001c0014t0002g0170 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2625-615A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981860 | |||||||
| chr5:140981881 | C | T | 1 | a0002c0008t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2625-594C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981881 | |||||||
| chr5:140981959 | A | C | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2625-516A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140981959 | |||||||
| chr5:140982339 | T | G | 11 | a0001c0001t0001g0177 a0001c0001t0020g0065 a0001c0003t0001g0173 others(8): Show |
11 | HG00621.hp2 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2625-136T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140982339 | |||||||
| chr5:140982448 | G | A | 5 | a0001c0003t0001g0007 a0001c0003t0001g0024 a0001c0005t0007g0268 others(2): Show |
7 | HG01496.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2625-27G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 2/3 | chr5 | 140982448 | |||||||
| chr5:140982795 | A | ATG | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0005g0182 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.2713+246_2713+247d others(4): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140982795 | ||||||
| chr5:140983206 | C | G | 1 | a0001c0003t0001g0274 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2713+643C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140983206 | |||||||
| chr5:140983247 | G | A | 12 | a0001c0001t0001g0177 a0001c0003t0001g0173 a0001c0003t0001g0174 others(9): Show |
12 | HG00621.hp2 HG01106.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2713+684G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140983247 | |||||||
| chr5:140983885 | T | C | 14 | a0001c0001t0001g0177 a0001c0002t0001g0198 a0001c0003t0001g0173 others(11): Show |
14 | HG00621.hp2 HG01106.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2713+1322T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140983885 | |||||||
| chr5:140983897 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(294): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.2713+1334G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140983897 | |||||||
| chr5:140984045 | T | C | 9 | a0001c0001t0001g0177 a0001c0003t0001g0173 a0001c0003t0001g0174 others(6): Show |
9 | HG00621.hp2 HG01106.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2713+1482T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984045 | |||||||
| chr5:140984174 | G | A | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2713+1611G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984174 | |||||||
| chr5:140984281 | C | G | 1 | a0001c0002t0001g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2713+1718C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984281 | |||||||
| chr5:140984395 | G | A | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2713+1832G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984395 | |||||||
| chr5:140984413 | C | A | 1 | a0001c0003t0001g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2713+1850C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984413 | |||||||
| chr5:140984687 | T | C | 1 | a0001c0002t0001g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2713+2124T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984687 | |||||||
| chr5:140984726 | A | C | 1 | a0001c0002t0001g0186 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2713+2163A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984726 | |||||||
| chr5:140984794 | A | C | 1 | a0001c0016t0001g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2713+2231A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984794 | |||||||
| chr5:140984945 | CT | C | 13 | a0001c0001t0001g0177 a0001c0003t0001g0173 a0001c0003t0001g0174 others(10): Show |
13 | HG00621.hp2 HG01106.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2713+2392delT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140984945 | ||||||
| chr5:140984982 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2713+2419G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140984982 | |||||||
| chr5:140985039 | G | A | 3 | a0001c0003t0002g0270 a0001c0014t0002g0170 a0002c0008t0001g0273 |
3 | HG01884.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2713+2476G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985039 | |||||||
| chr5:140985065 | G | A | 2 | a0001c0009t0001g0199 a0001c0009t0001g0200 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2713+2502G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985065 | |||||||
| chr5:140985509 | T | C | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2713+2946T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985509 | |||||||
| chr5:140985540 | T | C | 1 | a0001c0020t0001g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2713+2977T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985540 | |||||||
| chr5:140985608 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2713+3045G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985608 | |||||||
| chr5:140985739 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0037 others(113): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2713+3196dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140985739 | ||||||
| chr5:140985739 | C | CTT | 15 | a0001c0001t0001g0064 a0001c0001t0001g0089 a0001c0001t0001g0137 others(12): Show |
15 | HG00438.hp1 HG00609.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2713+3195_2713+319 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140985739 | ||||||
| chr5:140985739 | CT | C | 8 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0002t0001g0050 others(5): Show |
8 | HG01884.hp1 HG02040.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2713+3196delT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140985739 | ||||||
| chr5:140985803 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0123 |
2 | NA18972.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2713+3240G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985803 | |||||||
| chr5:140985930 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2713+3367G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140985930 | |||||||
| chr5:140986019 | G | A | 1 | a0001c0005t0007g0268 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2713+3456G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140986019 | |||||||
| chr5:140986130 | G | T | 1 | a0001c0004t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2713+3567G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140986130 | |||||||
| chr5:140986372 | G | A | 1 | a0001c0001t0004g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2713+3809G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140986372 | |||||||
| chr5:140986653 | A | T | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2713+4090A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140986653 | |||||||
| chr5:140987011 | C | T | 2 | a0001c0005t0007g0043 a0001c0005t0007g0044 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2713+4448C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987011 | |||||||
| chr5:140987075 | G | A | 3 | a0001c0001t0001g0090 a0001c0002t0001g0196 a0001c0002t0015g0197 |
3 | NA18952.hp1 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2713+4512G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987075 | |||||||
| chr5:140987106 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0005g0182 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.2713+4543C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987106 | |||||||
| chr5:140987139 | G | A | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02040.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2713+4576G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987139 | |||||||
| chr5:140987213 | C | CA | 14 | a0001c0001t0001g0017 a0001c0001t0001g0177 a0001c0001t0001g0181 others(11): Show |
15 | HG00323.hp1 HG00621.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2713+4664dupA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140987213 | ||||||
| chr5:140987224 | A | AT | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0005g0190 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.2713+4661_2713+466 others(5): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987224 | |||||||
| chr5:140987225 | A | T | 4 | a0001c0002t0001g0160 a0001c0002t0010g0248 a0001c0002t0010g0249 others(1): Show |
4 | HG02074.hp2 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2713+4662A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987225 | |||||||
| chr5:140987228 | T | A | 2 | a0001c0001t0006g0279 a0001c0001t0006g0280 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2713+4665T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987228 | |||||||
| chr5:140987235 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2713+4672T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987235 | |||||||
| chr5:140987268 | C | T | 1 | a0001c0003t0019g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2713+4705C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987268 | |||||||
| chr5:140987316 | G | A | 28 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0033 others(25): Show |
30 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2713+4753G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987316 | |||||||
| chr5:140987318 | A | C | 1 | a0001c0004t0001g0294 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2713+4755A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987318 | |||||||
| chr5:140987474 | G | A | 1 | a0002c0008t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2713+4911G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987474 | |||||||
| chr5:140987536 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2713+4973A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987536 | |||||||
| chr5:140987690 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0061 others(71): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2713+5127T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987690 | |||||||
| chr5:140987850 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2713+5287A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140987850 | |||||||
| chr5:140988043 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2713+5480A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140988043 | |||||||
| chr5:140988093 | G | A | 17 | a0001c0001t0001g0061 a0001c0001t0001g0247 a0001c0001t0001g0295 others(14): Show |
20 | HG00423.hp2 HG01993.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.2713+5530G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140988093 | |||||||
| chr5:140988182 | G | A | 1 | a0001c0002t0003g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2713+5619G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140988182 | |||||||
| chr5:140988308 | G | T | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2713+5745G>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140988308 | |||||||
| chr5:140988623 | T | C | 1 | a0001c0005t0007g0268 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2713+6060T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140988623 | |||||||
| chr5:140988764 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2713+6201G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140988764 | |||||||
| chr5:140989274 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0061 others(83): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.2713+6711G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140989274 | |||||||
| chr5:140989533 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2713+6970T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140989533 | |||||||
| chr5:140989601 | A | C | 1 | a0001c0002t0010g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2713+7038A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140989601 | |||||||
| chr5:140989733 | C | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0026 others(263): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2713+7170C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140989733 | |||||||
| chr5:140989805 | A | G | 29 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0033 others(26): Show |
31 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2713+7242A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140989805 | |||||||
| chr5:140989949 | G | A | 1 | a0001c0004t0001g0294 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2713+7386G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140989949 | |||||||
| chr5:140990084 | C | T | 16 | a0001c0001t0020g0065 a0001c0002t0003g0051 a0001c0002t0003g0055 others(13): Show |
16 | HG01175.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2713+7521C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990084 | |||||||
| chr5:140990199 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2713+7636G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990199 | |||||||
| chr5:140990426 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0061 others(88): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2713+7863G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990426 | |||||||
| chr5:140990443 | A | G | 4 | a0001c0002t0002g0099 a0001c0002t0008g0049 a0001c0002t0008g0098 others(1): Show |
4 | NA18957.hp2 NA18995.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2713+7880A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990443 | |||||||
| chr5:140990586 | A | G | 1 | a0001c0002t0003g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2713+8023A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990586 | |||||||
| chr5:140990621 | G | A | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2713+8058G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990621 | |||||||
| chr5:140990754 | G | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(13): Show |
18 | HG00609.hp1 HG00673.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.2713+8191G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990754 | |||||||
| chr5:140990983 | A | G | 16 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(13): Show |
18 | HG00609.hp1 HG00673.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.2713+8420A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140990983 | |||||||
| chr5:140991183 | A | G | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2713+8620A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991183 | |||||||
| chr5:140991523 | T | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0005g0182 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.2713+8960T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991523 | |||||||
| chr5:140991746 | T | C | 1 | a0001c0003t0001g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2713+9183T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991746 | |||||||
| chr5:140991799 | G | A | 1 | a0002c0008t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2713+9236G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991799 | |||||||
| chr5:140991900 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2713+9337A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991900 | |||||||
| chr5:140991968 | C | A | 6 | a0001c0001t0006g0279 a0001c0001t0006g0280 a0001c0002t0001g0198 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2713+9405C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991968 | |||||||
| chr5:140991985 | A | G | 1 | a0001c0002t0001g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2713+9422A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140991985 | |||||||
| chr5:140992017 | C | CTG | 59 | a0001c0001t0001g0053 a0001c0001t0001g0072 a0001c0001t0001g0073 others(56): Show |
60 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2713+9490_2713+949 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140992017 | ||||||
| chr5:140992017 | C | CTGTG | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0071 others(6): Show |
9 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2713+9488_2713+949 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140992017 | ||||||
| chr5:140992017 | C | CTGTGTG | 3 | a0001c0002t0003g0059 a0001c0002t0012g0054 a0001c0003t0001g0024 |
3 | HG01496.hp2 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2713+9486_2713+949 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140992017 | ||||||
| chr5:140992017 | C | CTGTGTGT others(3): Show |
1 | a0001c0003t0001g0007 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2713+9482_2713+949 others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140992017 | ||||||
| chr5:140992017 | CTG | C | 48 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0161 others(45): Show |
52 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2713+9490_2713+949 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140992017 | ||||||
| chr5:140992017 | CTGTG | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0090 others(76): Show |
93 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2713+9488_2713+949 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140992017 | ||||||
| chr5:140992060 | A | T | 2 | a0001c0002t0001g0221 a0001c0002t0001g0263 |
2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2713+9497A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992060 | |||||||
| chr5:140992270 | G | A | 1 | a0001c0003t0001g0266 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2713+9707G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992270 | |||||||
| chr5:140992285 | A | G | 1 | a0001c0002t0003g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2713+9722A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992285 | |||||||
| chr5:140992416 | C | T | 28 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0033 others(25): Show |
30 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2713+9853C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992416 | |||||||
| chr5:140992637 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0026 others(205): Show |
228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2713+10074G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992637 | |||||||
| chr5:140992691 | G | A | 1 | a0001c0014t0002g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2713+10128G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992691 | |||||||
| chr5:140992812 | G | A | 2 | a0001c0002t0001g0221 a0001c0002t0001g0263 |
2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2713+10249G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992812 | |||||||
| chr5:140992925 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2713+10362C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140992925 | |||||||
| chr5:140993185 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2713+10622G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993185 | |||||||
| chr5:140993203 | A | AT | 5 | a0001c0002t0012g0054 a0001c0003t0001g0007 a0001c0003t0001g0024 others(2): Show |
7 | HG01496.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2713+10647dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993203 | ||||||
| chr5:140993262 | C | T | 2 | a0001c0003t0019g0282 a0001c0005t0014g0025 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2713+10699C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993262 | |||||||
| chr5:140993270 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2713+10707G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993270 | |||||||
| chr5:140993282 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2713+10719C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993282 | |||||||
| chr5:140993289 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2713+10726C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993289 | |||||||
| chr5:140993345 | C | T | 1 | a0001c0005t0014g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2713+10782C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993345 | |||||||
| chr5:140993460 | T | TCC | 3 | a0001c0001t0006g0279 a0002c0006t0006g0020 a0002c0006t0006g0021 |
3 | HG02109.hp2 HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2713+10898_2713+10 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993460 | ||||||
| chr5:140993460 | TCTCACAC others(13): Show |
T | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2713+10899_2713+10 others(26): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993460 | ||||||
| chr5:140993462 | T | A | 6 | a0001c0001t0001g0137 a0001c0001t0006g0279 a0001c0003t0009g0271 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2713+10899T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993462 | |||||||
| chr5:140993462 | T | C | 2 | a0001c0001t0006g0280 a0002c0006t0006g0022 |
2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2713+10899T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993462 | |||||||
| chr5:140993462 | T | TCA | 33 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(30): Show |
35 | HG00280.hp1 HG00609.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2713+10945_2713+10 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | T | TCACA | 20 | a0001c0001t0001g0052 a0001c0001t0001g0072 a0001c0001t0001g0089 others(17): Show |
20 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.2713+10943_2713+10 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | T | TCACACA | 10 | a0001c0001t0001g0076 a0001c0001t0001g0100 a0001c0001t0001g0106 others(7): Show |
11 | HG00323.hp1 HG00738.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2713+10941_2713+10 others(12): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | T | TCACACAC others(5): Show |
1 | a0001c0020t0001g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2713+10935_2713+10 others(18): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCA | T | 35 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0075 others(32): Show |
35 | HG00621.hp2 HG01099.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.2713+10945_2713+10 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACA | T | 47 | a0001c0001t0001g0026 a0001c0001t0001g0086 a0001c0001t0001g0087 others(44): Show |
48 | HG00140.hp2 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.2713+10943_2713+10 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACACA | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0090 others(61): Show |
78 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.2713+10941_2713+10 others(12): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACACAC others(1): Show |
T | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.2713+10939_2713+10 others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0001g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2713+10937_2713+10 others(16): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACACAC others(5): Show |
T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2713+10935_2713+10 others(18): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACACAC others(7): Show |
T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0005t0007g0042 others(2): Show |
5 | HG01167.hp2 HG02257.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2713+10933_2713+10 others(20): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993462 | TCACACAC others(13): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2713+10927_2713+10 others(26): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993462 | ||||||
| chr5:140993482 | A | C | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2713+10919A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993482 | |||||||
| chr5:140993501 | C | CAT | 3 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0158 |
3 | HG02083.hp1 NA18983.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.2713+10939_2713+10 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993501 | ||||||
| chr5:140993523 | CAG | C | 6 | a0001c0001t0006g0279 a0001c0001t0006g0280 a0001c0002t0001g0198 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2713+10974_2713+10 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140993523 | ||||||
| chr5:140993668 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2713+11105A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993668 | |||||||
| chr5:140993767 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02630.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2713+11204G>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993767 | |||||||
| chr5:140993861 | T | G | 2 | a0001c0001t0001g0161 a0001c0002t0001g0222 |
2 | NA18989.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2713+11298T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140993861 | |||||||
| chr5:140994248 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2713+11685G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994248 | |||||||
| chr5:140994249 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0061 others(83): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.2713+11686G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994249 | |||||||
| chr5:140994303 | C | T | 28 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0033 others(25): Show |
30 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2713+11740C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994303 | |||||||
| chr5:140994539 | CA | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0039 others(162): Show |
185 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.2713+11984delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140994539 | ||||||
| chr5:140994560 | C | T | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2713+11997C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994560 | |||||||
| chr5:140994788 | C | T | 4 | a0001c0002t0002g0099 a0001c0002t0008g0049 a0001c0002t0008g0098 others(1): Show |
4 | NA18957.hp2 NA18995.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2713+12225C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994788 | |||||||
| chr5:140994812 | A | G | 1 | a0001c0002t0011g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2713+12249A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994812 | |||||||
| chr5:140994850 | CAT | C | 6 | a0001c0001t0006g0279 a0001c0001t0006g0280 a0001c0002t0001g0198 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2713+12288_2713+12 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140994850 | |||||||
| chr5:140995000 | T | C | 1 | a0001c0001t0006g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2713+12437T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995000 | |||||||
| chr5:140995109 | C | G | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2713+12546C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995109 | |||||||
| chr5:140995338 | C | T | 1 | a0001c0003t0002g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2713+12775C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995338 | |||||||
| chr5:140995361 | G | C | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2713+12798G>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995361 | |||||||
| chr5:140995570 | A | T | 1 | a0001c0003t0002g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2713+13007A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995570 | |||||||
| chr5:140995742 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2713+13179A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995742 | |||||||
| chr5:140995948 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2713+13385C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140995948 | |||||||
| chr5:140996386 | C | G | 1 | a0001c0002t0001g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2714-13241C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140996386 | |||||||
| chr5:140996691 | C | A | 2 | a0001c0002t0005g0191 a0001c0002t0005g0192 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2714-12936C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140996691 | |||||||
| chr5:140996918 | A | T | 2 | a0001c0002t0010g0248 a0001c0002t0010g0250 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2714-12709A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140996918 | |||||||
| chr5:140997091 | G | A | 2 | a0001c0003t0001g0261 a0002c0008t0001g0260 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2714-12536G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997091 | |||||||
| chr5:140997121 | A | G | 2 | a0001c0002t0001g0011 a0001c0002t0001g0184 |
3 | NA18942.hp2 NA18987.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2714-12506A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997121 | |||||||
| chr5:140997129 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2714-12498C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997129 | |||||||
| chr5:140997131 | C | T | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-12496C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997131 | |||||||
| chr5:140997261 | C | T | 1 | a0001c0001t0006g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2714-12366C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997261 | |||||||
| chr5:140997328 | G | A | 3 | a0001c0002t0011g0269 a0001c0003t0019g0282 a0001c0005t0014g0025 |
3 | HG02055.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2714-12299G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997328 | |||||||
| chr5:140997438 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2714-12189A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997438 | |||||||
| chr5:140997506 | T | A | 3 | a0001c0005t0007g0042 a0001c0005t0007g0043 a0001c0005t0007g0044 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2714-12121T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997506 | |||||||
| chr5:140997511 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0127 |
3 | HG02735.hp2 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2714-12116G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997511 | |||||||
| chr5:140997668 | T | TTG | 26 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0053 others(23): Show |
27 | HG00438.hp2 HG00741.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2714-11931_2714-11 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140997668 | ||||||
| chr5:140997668 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0177 a0001c0003t0001g0173 a0001c0003t0001g0174 others(6): Show |
9 | HG00621.hp2 HG02155.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2714-11937_2714-11 others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140997668 | ||||||
| chr5:140997668 | TTG | T | 56 | a0001c0001t0001g0026 a0001c0001t0001g0095 a0001c0001t0001g0106 others(53): Show |
59 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2714-11931_2714-11 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140997668 | ||||||
| chr5:140997668 | TTGTG | T | 4 | a0001c0002t0001g0267 a0001c0003t0002g0270 a0001c0014t0002g0170 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714-11933_2714-11 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140997668 | ||||||
| chr5:140997740 | C | T | 1 | a0001c0002t0010g0249 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2714-11887C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997740 | |||||||
| chr5:140997897 | A | C | 29 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0033 others(26): Show |
31 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2714-11730A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140997897 | |||||||
| chr5:140998188 | AG | A | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2714-11438delG | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140998188 | |||||||
| chr5:140998438 | A | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2714-11189A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140998438 | |||||||
| chr5:140998569 | G | GT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0040 others(111): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.2714-11046dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140998569 | ||||||
| chr5:140998569 | G | GTT | 31 | a0001c0001t0001g0017 a0001c0001t0001g0177 a0001c0001t0001g0181 others(28): Show |
34 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2714-11047_2714-11 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140998569 | ||||||
| chr5:140998569 | GT | G | 44 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0071 others(41): Show |
44 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.2714-11046delT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140998569 | ||||||
| chr5:140998611 | C | A | 2 | a0001c0003t0001g0173 a0001c0003t0001g0174 |
2 | HG00621.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.2714-11016C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140998611 | |||||||
| chr5:140998715 | C | T | 1 | a0001c0003t0002g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2714-10912C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140998715 | |||||||
| chr5:140998756 | G | A | 4 | a0001c0001t0001g0247 a0001c0001t0001g0295 a0001c0002t0001g0188 others(1): Show |
4 | NA18947.hp2 NA18964.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714-10871G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140998756 | |||||||
| chr5:140998902 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714-10725C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140998902 | |||||||
| chr5:140999024 | T | C | 9 | a0001c0001t0006g0279 a0001c0001t0006g0280 a0001c0002t0001g0198 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2714-10603T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999024 | |||||||
| chr5:140999070 | T | A | 1 | a0001c0002t0010g0248 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2714-10557T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999070 | |||||||
| chr5:140999076 | C | G | 1 | a0001c0002t0001g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2714-10551C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999076 | |||||||
| chr5:140999139 | C | T | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2714-10488C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999139 | |||||||
| chr5:140999346 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2714-10281T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999346 | |||||||
| chr5:140999398 | A | G | 37 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0033 others(34): Show |
39 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2714-10229A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999398 | |||||||
| chr5:140999523 | C | A | 1 | a0001c0003t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2714-10104C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999523 | |||||||
| chr5:140999654 | C | T | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-9973C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999654 | |||||||
| chr5:140999666 | G | A | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-9961G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999666 | |||||||
| chr5:140999690 | G | A | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2714-9937G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 140999690 | |||||||
| chr5:140999693 | A | AT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(2): Show |
6 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-9925dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 140999693 | ||||||
| chr5:141000102 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2714-9525C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000102 | |||||||
| chr5:141000188 | A | G | 1 | a0001c0003t0001g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2714-9439A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000188 | |||||||
| chr5:141000192 | T | C | 5 | a0001c0003t0001g0275 a0001c0003t0001g0276 a0001c0003t0001g0277 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2714-9435T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000192 | |||||||
| chr5:141000279 | G | A | 1 | a0001c0005t0007g0268 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2714-9348G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000279 | |||||||
| chr5:141000351 | GTCTCTCT others(7): Show |
G | 1 | a0001c0003t0002g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2714-9266_2714-925 others(18): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000351 | ||||||
| chr5:141000361 | G | GTC | 11 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0151 others(8): Show |
12 | HG00642.hp2 HG00738.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.2714-9232_2714-923 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000361 | ||||||
| chr5:141000361 | GTC | G | 8 | a0001c0001t0001g0076 a0001c0001t0001g0140 a0001c0001t0002g0034 others(5): Show |
9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2714-9232_2714-923 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000361 | ||||||
| chr5:141000361 | GTCTC | G | 54 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0110 others(51): Show |
56 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2714-9234_2714-923 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000361 | ||||||
| chr5:141000361 | GTCTCTC | G | 65 | a0001c0001t0001g0039 a0001c0001t0001g0090 a0001c0001t0001g0177 others(62): Show |
70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.2714-9236_2714-923 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000361 | ||||||
| chr5:141000361 | GTCTCTCT others(1): Show |
G | 9 | a0001c0002t0001g0188 a0001c0002t0001g0207 a0001c0002t0001g0245 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.2714-9238_2714-923 others(12): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000361 | ||||||
| chr5:141000361 | GTCTCTCT others(3): Show |
G | 2 | a0001c0002t0001g0198 a0001c0005t0007g0043 |
2 | HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2714-9240_2714-923 others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000361 | ||||||
| chr5:141000383 | CTCTCTCT others(7): Show |
C | 1 | a0001c0002t0001g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2714-9242_2714-922 others(18): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000383 | ||||||
| chr5:141000385 | CTCTCTCT others(5): Show |
C | 1 | a0001c0002t0001g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2714-9240_2714-922 others(16): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000385 | ||||||
| chr5:141000385 | CTCTCTCT others(7): Show |
C | 3 | a0001c0002t0005g0191 a0001c0002t0005g0192 a0001c0019t0011g0067 |
3 | HG01069.hp1 HG01071.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2714-9240_2714-922 others(18): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000385 | ||||||
| chr5:141000387 | C | A | 1 | a0001c0003t0001g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2714-9240C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000387 | |||||||
| chr5:141000387 | CTCTCTCT others(3): Show |
C | 1 | a0001c0002t0005g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2714-9238_2714-922 others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000387 | ||||||
| chr5:141000387 | CTCTCTCT others(7): Show |
C | 1 | a0001c0002t0012g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2714-9238_2714-922 others(18): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000387 | ||||||
| chr5:141000389 | C | A | 8 | a0001c0001t0002g0034 a0001c0001t0002g0097 a0001c0001t0002g0169 others(5): Show |
8 | HG00323.hp2 HG00609.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.2714-9238C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000389 | |||||||
| chr5:141000389 | CTCTCTCT others(1): Show |
C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0002t0001g0011 others(5): Show |
8 | HG01099.hp1 HG01106.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2714-9236_2714-922 others(12): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000389 | ||||||
| chr5:141000389 | CTCTCTCT others(3): Show |
C | 1 | a0001c0002t0005g0193 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2714-9236_2714-922 others(14): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000389 | ||||||
| chr5:141000391 | C | A | 19 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0001g0140 others(16): Show |
20 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.2714-9236C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000391 | |||||||
| chr5:141000391 | CTCTCTA | C | 20 | a0001c0001t0001g0205 a0001c0001t0001g0227 a0001c0001t0001g0236 others(17): Show |
20 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-9234_2714-922 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000391 | ||||||
| chr5:141000391 | CTCTCTAT others(1): Show |
C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0001g0010 others(3): Show |
6 | HG00741.hp1 HG01167.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-9234_2714-922 others(12): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000391 | ||||||
| chr5:141000393 | C | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0111 others(45): Show |
49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.2714-9234C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000393 | |||||||
| chr5:141000393 | C | CTA | 3 | a0001c0001t0004g0129 a0001c0001t0004g0148 a0001c0004t0001g0008 |
3 | HG01346.hp2 NA18966.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.2714-9233_2714-923 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000393 | ||||||
| chr5:141000393 | CTCTA | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0220 others(1): Show |
4 | HG00741.hp2 HG03139.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714-9232_2714-922 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000393 | ||||||
| chr5:141000393 | CTCTATA | C | 4 | a0001c0001t0001g0001 a0001c0002t0001g0222 a0001c0004t0001g0291 others(1): Show |
4 | HG00280.hp2 HG02027.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714-9232_2714-922 others(10): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000393 | ||||||
| chr5:141000395 | C | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0052 others(113): Show |
121 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2714-9232C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000395 | |||||||
| chr5:141000395 | C | CTA | 5 | a0001c0001t0001g0087 a0001c0001t0001g0162 a0001c0001t0004g0066 others(2): Show |
5 | HG00423.hp1 HG02572.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2714-9206_2714-920 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000395 | ||||||
| chr5:141000397 | A | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(43): Show |
48 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2714-9230A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000397 | |||||||
| chr5:141000399 | A | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0037 others(23): Show |
28 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.2714-9228A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000399 | |||||||
| chr5:141000401 | A | C | 12 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0080 others(9): Show |
13 | HG00642.hp2 HG01175.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.2714-9226A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000401 | |||||||
| chr5:141000403 | A | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0152 others(1): Show |
4 | HG00642.hp2 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2714-9224A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000403 | |||||||
| chr5:141000405 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2714-9222A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000405 | |||||||
| chr5:141000415 | A | T | 1 | a0001c0014t0002g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2714-9212A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000415 | |||||||
| chr5:141000416 | TA | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0096 others(2): Show |
6 | HG00609.hp1 HG02738.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2714-9210delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000416 | |||||||
| chr5:141000417 | A | T | 4 | a0001c0001t0002g0169 a0001c0003t0002g0035 a0001c0003t0002g0270 others(1): Show |
4 | HG00673.hp2 HG01884.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.2714-9210A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000417 | |||||||
| chr5:141000418 | TA | T | 21 | a0001c0001t0001g0113 a0001c0001t0001g0131 a0001c0001t0001g0177 others(18): Show |
22 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.2714-9208delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000418 | |||||||
| chr5:141000419 | A | T | 28 | a0001c0001t0001g0041 a0001c0001t0001g0100 a0001c0001t0001g0111 others(25): Show |
29 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2714-9208A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000419 | |||||||
| chr5:141000420 | TA | T | 24 | a0001c0001t0001g0061 a0001c0001t0001g0227 a0001c0001t0001g0247 others(21): Show |
26 | HG00673.hp1 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2714-9206delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000420 | |||||||
| chr5:141000421 | A | AT | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0154 others(3): Show |
6 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-9183dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000421 | ||||||
| chr5:141000421 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0039 others(122): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2714-9206A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000421 | |||||||
| chr5:141000421 | AT | A | 18 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0052 others(15): Show |
18 | HG01099.hp1 HG01515.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.2714-9183delT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000421 | ||||||
| chr5:141000421 | ATTT | A | 8 | a0001c0001t0001g0053 a0001c0001t0001g0085 a0001c0001t0001g0115 others(5): Show |
8 | HG00408.hp2 HG00438.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.2714-9185_2714-918 others(7): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000421 | ||||||
| chr5:141000421 | ATTTT | A | 9 | a0001c0001t0001g0082 a0001c0001t0001g0092 a0001c0001t0001g0289 others(6): Show |
9 | HG01071.hp1 HG01261.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.2714-9186_2714-918 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000421 | ||||||
| chr5:141000422 | T | TA | 5 | a0001c0001t0001g0086 a0001c0001t0001g0138 a0001c0001t0001g0145 others(2): Show |
5 | HG02145.hp2 NA18952.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.2714-9205_2714-920 others(5): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000422 | |||||||
| chr5:141000423 | T | A | 38 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0071 others(35): Show |
39 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.2714-9204T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000423 | |||||||
| chr5:141000424 | T | A | 10 | a0001c0001t0001g0045 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.2714-9203T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000424 | |||||||
| chr5:141000425 | T | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0071 others(12): Show |
16 | HG00642.hp1 HG01175.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2714-9202T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000425 | |||||||
| chr5:141000426 | T | A | 1 | a0001c0001t0001g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2714-9201T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000426 | |||||||
| chr5:141000427 | T | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0289 others(3): Show |
6 | HG01071.hp1 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-9200T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000427 | |||||||
| chr5:141000538 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0039 others(160): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2714-9089A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000538 | |||||||
| chr5:141000578 | C | T | 1 | a0001c0003t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2714-9049C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000578 | |||||||
| chr5:141000587 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2714-9040C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000587 | |||||||
| chr5:141000611 | A | T | 3 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0001c0002t0001g0244 |
3 | HG00741.hp2 HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2714-9016A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000611 | |||||||
| chr5:141000648 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2714-8979G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141000648 | |||||||
| chr5:141000743 | T | TA | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0001g0198 others(7): Show |
10 | HG01071.hp2 HG01167.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2714-8872dupA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141000743 | ||||||
| chr5:141001278 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0284 |
3 | HG01175.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2714-8349C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141001278 | |||||||
| chr5:141001288 | C | T | 9 | a0001c0001t0001g0177 a0001c0003t0001g0173 a0001c0003t0001g0174 others(6): Show |
9 | HG00621.hp2 HG01106.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2714-8339C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141001288 | |||||||
| chr5:141001314 | T | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-8313T>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141001314 | |||||||
| chr5:141001822 | TGACAGAG others(5): Show |
T | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-7795_2714-778 others(16): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141001822 | ||||||
| chr5:141002363 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0131 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2714-7264A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141002363 | |||||||
| chr5:141002532 | C | T | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-7095C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141002532 | |||||||
| chr5:141002656 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0131 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2714-6971C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141002656 | |||||||
| chr5:141002682 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2714-6945G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141002682 | |||||||
| chr5:141003093 | C | T | 2 | a0001c0002t0001g0011 a0001c0002t0001g0184 |
3 | NA18942.hp2 NA18987.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2714-6534C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141003093 | |||||||
| chr5:141003197 | C | T | 3 | a0002c0006t0006g0020 a0002c0006t0006g0021 a0002c0006t0006g0022 |
3 | HG02109.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2714-6430C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141003197 | |||||||
| chr5:141003207 | T | C | 2 | a0001c0002t0001g0185 a0001c0002t0016g0264 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2714-6420T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141003207 | |||||||
| chr5:141003476 | C | G | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-6151C>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141003476 | |||||||
| chr5:141003608 | C | T | 1 | a0001c0003t0001g0036 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2714-6019C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141003608 | |||||||
| chr5:141003751 | T | G | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-5876T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141003751 | |||||||
| chr5:141004046 | C | A | 1 | a0001c0002t0001g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2714-5581C>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141004046 | |||||||
| chr5:141004391 | G | A | 1 | a0001c0001t0004g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2714-5236G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141004391 | |||||||
| chr5:141004637 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0283 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2714-4990A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141004637 | |||||||
| chr5:141004952 | C | T | 1 | a0001c0003t0002g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2714-4675C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141004952 | |||||||
| chr5:141005371 | T | G | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-4256T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005371 | |||||||
| chr5:141005488 | G | A | 6 | a0001c0002t0001g0234 a0001c0002t0012g0054 a0001c0003t0001g0007 others(3): Show |
8 | HG01496.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2714-4139G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005488 | |||||||
| chr5:141005520 | G | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(14): Show |
19 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2714-4107G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005520 | |||||||
| chr5:141005696 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2714-3931C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005696 | |||||||
| chr5:141005701 | C | CA | 63 | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0076 others(60): Show |
63 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.2714-3896dupA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141005701 | ||||||
| chr5:141005701 | C | CAA | 14 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
15 | HG01167.hp2 HG01175.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.2714-3897_2714-389 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141005701 | ||||||
| chr5:141005701 | C | CAAAA | 9 | a0001c0001t0001g0177 a0001c0002t0005g0191 a0001c0002t0005g0192 others(6): Show |
9 | HG00621.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2714-3899_2714-389 others(8): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141005701 | ||||||
| chr5:141005701 | CA | C | 9 | a0001c0001t0001g0106 a0001c0001t0002g0034 a0001c0001t0004g0134 others(6): Show |
9 | HG01168.hp2 HG01256.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2714-3896delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141005701 | ||||||
| chr5:141005701 | CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-3907_2714-389 others(16): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141005701 | ||||||
| chr5:141005783 | C | T | 32 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(29): Show |
36 | HG00609.hp1 HG00673.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.2714-3844C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005783 | |||||||
| chr5:141005917 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2714-3710A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005917 | |||||||
| chr5:141005932 | G | A | 1 | a0001c0001t0002g0097 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2714-3695G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141005932 | |||||||
| chr5:141006011 | G | A | 1 | a0001c0002t0003g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2714-3616G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006011 | |||||||
| chr5:141006105 | G | GT | 15 | a0001c0001t0006g0280 a0001c0002t0005g0182 a0001c0002t0005g0190 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2714-3508dupT | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141006105 | ||||||
| chr5:141006125 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2714-3502G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006125 | |||||||
| chr5:141006216 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0061 others(82): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.2714-3411A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006216 | |||||||
| chr5:141006221 | T | C | 1 | a0001c0003t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2714-3406T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006221 | |||||||
| chr5:141006390 | T | G | 1 | a0001c0002t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2714-3237T>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006390 | |||||||
| chr5:141006474 | A | G | 2 | a0001c0003t0002g0270 a0001c0014t0002g0170 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2714-3153A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006474 | |||||||
| chr5:141006491 | G | A | 8 | a0001c0002t0001g0234 a0001c0002t0012g0054 a0001c0003t0001g0007 others(5): Show |
10 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2714-3136G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006491 | |||||||
| chr5:141006916 | A | G | 5 | a0001c0001t0006g0279 a0001c0001t0006g0280 a0002c0006t0006g0020 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2714-2711A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141006916 | |||||||
| chr5:141007324 | A | G | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-2303A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141007324 | |||||||
| chr5:141007377 | A | C | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-2250A>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141007377 | |||||||
| chr5:141007395 | C | CA | 6 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0001g0135 others(3): Show |
6 | HG00621.hp1 HG02027.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-2209dupA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141007395 | ||||||
| chr5:141007395 | CA | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0026 others(186): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2714-2209delA | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141007395 | ||||||
| chr5:141007395 | CAA | C | 9 | a0001c0001t0001g0092 a0001c0001t0002g0047 a0001c0001t0002g0083 others(6): Show |
9 | HG01257.hp2 HG02896.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2714-2210_2714-220 others(6): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141007395 | ||||||
| chr5:141007395 | CAAA | C | 13 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(10): Show |
15 | HG00609.hp1 HG00673.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.2714-2211_2714-220 others(7): Show |
PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr5 | 141007395 | ||||||
| chr5:141007689 | A | G | 1 | a0001c0003t0002g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2714-1938A>G | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141007689 | |||||||
| chr5:141007748 | T | C | 1 | a0001c0004t0002g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2714-1879T>C | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141007748 | |||||||
| chr5:141008375 | C | T | 1 | a0001c0004t0001g0297 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2714-1252C>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141008375 | |||||||
| chr5:141008440 | A | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0159 |
2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2714-1187A>T | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141008440 | |||||||
| chr5:141008698 | G | A | 11 | a0001c0002t0003g0051 a0001c0002t0003g0055 a0001c0002t0003g0057 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2714-929G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141008698 | |||||||
| chr5:141008922 | G | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
20 | HG00609.hp1 HG00673.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2714-705G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141008922 | |||||||
| chr5:141008970 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2714-657G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141008970 | |||||||
| chr5:141009439 | G | A | 1 | a0001c0001t0004g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2714-188G>A | PCDHAC2 | ENSG00000243232.6 | transcript | ENST00000289269.7 | protein_coding | 3/3 | chr5 | 141009439 |