Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1911 |
| ensemblid | ENSG00000111752.11 |
| hgncid | 3182 |
| symbol | PHC1 |
| name | polyhomeotic homolog 1 |
| refseq_nuc | NM_004426.3 |
| refseq_prot | NP_004417.2 |
| ensembl_nuc | ENST00000544916.6 |
| ensembl_prot | ENSP00000437659.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 8914509 |
| end | 8941467 |
| strand | + |
| ver | v1.2 |
| region | chr12:8914509-8941467 |
| region5000 | chr12:8909509-8946467 |
| regionname0 | PHC1_chr12_8914509_8941467 |
| regionname5000 | PHC1_chr12_8909509_8946467 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1004 | 206 | 61 | 34 | 90 | 5 | 16 | 65 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0002 | 0/0 | 1004 | 129 | 13 | 27 | 75 | 6 | 8 | 64 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0003 | 0/0 | 1004 | 14 | 3 | 5 | 0 | 0 | 6 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0004 | 0/0 | 1002 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(997): Show |
chr12 | 8909509 | 8946467 |
| a0005 | 0/0 | 1004 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0006 | 0/0 | 1004 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0007 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0008 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0009 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(999): Show |
chr12 | 8909509 | 8946467 |
| a0010 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(587): Show |
chr12 | 8909509 | 8946467 |
| a0011 | 0/0 | 209 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(204): Show |
chr12 | 8909509 | 8946467 |
| a0012 | 0/0 | 632 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(627): Show |
chr12 | 8909509 | 8946467 |
| a0013 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(756): Show |
chr12 | 8909509 | 8946467 |
| a0014 | 0/0 | 160 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(155): Show |
chr12 | 8909509 | 8946467 |
| a0015 | 0/0 | 119 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(114): Show |
chr12 | 8909509 | 8946467 |
| a0016 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | METES others(481): Show |
chr12 | 8909509 | 8946467 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3012 | 87 | 34 | 11 | 41 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0003 | 0/0 | 3012 | 50 | 1 | 4 | 39 | 2 | 4 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0004 | 0/0 | 3012 | 32 | 5 | 14 | 2 | 2 | 9 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0005 | 0/0 | 3012 | 21 | 12 | 4 | 2 | 0 | 3 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0007 | 0/0 | 3012 | 11 | 4 | 1 | 6 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0010 | 0/0 | 3012 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0013 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0016 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0001c0026 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0002c0001 | 0/0 | 3012 | 124 | 9 | 26 | 75 | 6 | 8 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0002c0009 | 0/0 | 3012 | 3 | 3 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0002c0019 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0002c0023 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0003c0006 | 0/0 | 3012 | 14 | 3 | 5 | 0 | 0 | 6 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0004c0008 | 0/0 | 3006 | 6 | 6 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3001): Show |
chr12 | 8909509 | 8946467 | ||
| a0005c0011 | 0/0 | 3012 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0006c0014 | 0/0 | 3012 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0007c0020 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0008c0017 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0009c0024 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3007): Show |
chr12 | 8909509 | 8946467 | ||
| a0010c0015 | 0/0 | 3011 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3006): Show |
chr12 | 8909509 | 8946467 | ||
| a0011c0022 | 0/0 | 3011 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3006): Show |
chr12 | 8909509 | 8946467 | ||
| a0012c0018 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3008): Show |
chr12 | 8909509 | 8946467 | ||
| a0013c0025 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3008): Show |
chr12 | 8909509 | 8946467 | ||
| a0014c0027 | 0/0 | 3011 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3006): Show |
chr12 | 8909509 | 8946467 | ||
| a0015c0012 | 0/0 | 3011 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3006): Show |
chr12 | 8909509 | 8946467 | ||
| a0016c0021 | 0/0 | 3016 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | ATGGA others(3011): Show |
chr12 | 8909509 | 8946467 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 5390 | 63 | 13 | 8 | 41 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0002t0003 | 0/0 | 5390 | 19 | 16 | 3 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0002t0004 | 0/0 | 5388 | 4 | 4 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5383): Show |
chr12 | 8909509 | 8946467 |
| a0001c0002t0011 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0003t0001 | 0/0 | 5390 | 46 | 0 | 4 | 36 | 2 | 4 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0003t0002 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0001c0003t0003 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0003t0013 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0003t0018 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0004t0001 | 0/0 | 5390 | 30 | 5 | 12 | 2 | 2 | 9 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0004t0009 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0004t0017 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0005t0001 | 0/0 | 5390 | 19 | 11 | 4 | 1 | 0 | 3 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0005t0010 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0005t0012 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0007t0001 | 0/0 | 5390 | 6 | 0 | 0 | 6 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0007t0005 | 0/0 | 5390 | 3 | 2 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0007t0022 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0001c0007t0023 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0010t0001 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0013t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0016t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0001c0026t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0001 | 0/0 | 5390 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0002 | 0/0 | 5391 | 111 | 9 | 24 | 65 | 6 | 7 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0006 | 0/0 | 5391 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0007 | 0/0 | 5391 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0008 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0014 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0015 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0016 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0019 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0020 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0001t0021 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0009t0002 | 0/0 | 5391 | 3 | 3 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0019t0002 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0002c0023t0002 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0003c0006t0001 | 0/0 | 5390 | 14 | 3 | 5 | 0 | 0 | 6 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0004c0008t0002 | 0/0 | 5385 | 6 | 6 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5380): Show |
chr12 | 8909509 | 8946467 |
| a0005c0011t0002 | 0/0 | 5391 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0006c0014t0002 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0007c0020t0001 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0008c0017t0001 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0009c0024t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5385): Show |
chr12 | 8909509 | 8946467 |
| a0010c0015t0001 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5384): Show |
chr12 | 8909509 | 8946467 |
| a0011c0022t0001 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5384): Show |
chr12 | 8909509 | 8946467 |
| a0012c0018t0002 | 0/0 | 5392 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5387): Show |
chr12 | 8909509 | 8946467 |
| a0013c0025t0001 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5386): Show |
chr12 | 8909509 | 8946467 |
| a0014c0027t0001 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5384): Show |
chr12 | 8909509 | 8946467 |
| a0015c0012t0001 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5384): Show |
chr12 | 8909509 | 8946467 |
| a0016c0021t0001 | 0/0 | 5394 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | AGCCC others(5389): Show |
chr12 | 8909509 | 8946467 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0006 | 0/0 | 7 | 1 | 0 | 5 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0010 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0013 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0002t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0004 | 0/0 | 9 | 0 | 1 | 6 | 1 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0013g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0003t0018g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0004t0017g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0005t0012g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0022g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0007t0023g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0010t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0010t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0013t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0016t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0001c0026t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0001 | 0/0 | 15 | 0 | 2 | 11 | 1 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0014 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0008g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0014g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0015g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0001t0021g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0009t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0009t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0009t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0019t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0002c0023t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0003c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0004c0008t0002g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0004c0008t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0005c0011t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0005c0011t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0006c0014t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0007c0020t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0008c0017t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0009c0024t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0010c0015t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0011c0022t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0012c0018t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0013c0025t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0014c0027t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0015c0012t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| a0016c0021t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0002 | g0014 | EUR | GBR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00099 | hp2 | a0006 | c0014 | t0002 | g0151 | EUR | GBR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0001 | EUR | GBR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00140 | hp2 | a0002 | c0001 | t0002 | g0127 | EUR | GBR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00408 | hp1 | a0002 | c0001 | t0006 | g0003 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00544 | hp1 | a0002 | c0001 | t0002 | g0147 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00609 | hp1 | a0002 | c0001 | t0002 | g0155 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0027 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0168 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00639 | hp2 | a0002 | c0001 | t0002 | g0141 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0210 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00673 | hp2 | a0001 | c0003 | t0013 | g0005 | EAS | CHS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00733 | hp1 | a0001 | c0004 | t0009 | g0027 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00733 | hp2 | a0002 | c0001 | t0002 | g0044 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00735 | hp1 | a0001 | c0005 | t0001 | g0007 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0017 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00738 | hp1 | a0003 | c0006 | t0001 | g0161 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0056 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00741 | hp1 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG00741 | hp2 | a0002 | c0001 | t0002 | g0046 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0053 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01069 | hp2 | a0002 | c0001 | t0002 | g0028 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01070 | hp1 | a0002 | c0001 | t0002 | g0014 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01070 | hp2 | a0003 | c0006 | t0001 | g0166 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01071 | hp1 | a0003 | c0006 | t0001 | g0165 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01071 | hp2 | a0002 | c0001 | t0002 | g0028 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01074 | hp2 | a0002 | c0001 | t0002 | g0044 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01081 | hp2 | a0001 | c0005 | t0001 | g0037 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01099 | hp1 | a0007 | c0020 | t0001 | g0007 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01099 | hp2 | a0002 | c0001 | t0002 | g0046 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01106 | hp1 | a0002 | c0001 | t0002 | g0109 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0201 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01109 | hp1 | a0002 | c0001 | t0002 | g0108 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01109 | hp2 | a0001 | c0007 | t0005 | g0196 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0223 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01168 | hp1 | a0005 | c0011 | t0002 | g0150 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0222 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01175 | hp2 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01192 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0173 | AMR | PUR | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01256 | hp1 | a0002 | c0001 | t0021 | g0021 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01256 | hp2 | a0008 | c0017 | t0001 | g0015 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01261 | hp1 | a0002 | c0001 | t0002 | g0144 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0187 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01358 | hp1 | a0001 | c0004 | t0017 | g0215 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01358 | hp2 | a0002 | c0001 | t0002 | g0045 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01361 | hp2 | a0002 | c0001 | t0008 | g0021 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0053 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01516 | hp1 | a0002 | c0001 | t0002 | g0039 | EUR | IBS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0202 | EUR | IBS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0039 | EUR | IBS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0004 | EUR | IBS | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01884 | hp1 | a0001 | c0010 | t0001 | g0090 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01928 | hp2 | a0002 | c0001 | t0002 | g0126 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01934 | hp1 | a0002 | c0001 | t0002 | g0001 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0213 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01943 | hp1 | a0002 | c0001 | t0002 | g0116 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01943 | hp2 | a0002 | c0001 | t0002 | g0098 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01952 | hp1 | a0003 | c0006 | t0001 | g0049 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01952 | hp2 | a0002 | c0001 | t0002 | g0117 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01975 | hp1 | a0002 | c0001 | t0002 | g0149 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0008 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0125 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01978 | hp2 | a0001 | c0004 | t0001 | g0203 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01993 | hp1 | a0002 | c0019 | t0002 | g0152 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01993 | hp2 | a0003 | c0006 | t0001 | g0051 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02040 | hp1 | a0002 | c0001 | t0002 | g0134 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02055 | hp1 | a0001 | c0002 | t0011 | g0225 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02071 | hp1 | a0002 | c0001 | t0002 | g0040 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02071 | hp2 | a0001 | c0005 | t0012 | g0024 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02074 | hp1 | a0002 | c0001 | t0002 | g0043 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02129 | hp1 | a0002 | c0001 | t0002 | g0191 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02129 | hp2 | a0002 | c0001 | t0002 | g0041 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02135 | hp2 | a0001 | c0007 | t0001 | g0034 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02145 | hp1 | a0002 | c0001 | t0002 | g0099 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02257 | hp1 | a0003 | c0006 | t0001 | g0015 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0221 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02258 | hp1 | a0002 | c0009 | t0002 | g0095 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0045 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0008 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0220 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0169 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02300 | hp2 | a0005 | c0011 | t0002 | g0122 | AMR | PEL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0023 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02523 | hp1 | a0002 | c0001 | t0002 | g0105 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0027 | EAS | KHV | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02572 | hp1 | a0002 | c0001 | t0002 | g0103 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0054 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02602 | hp1 | a0002 | c0001 | t0002 | g0137 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02602 | hp2 | a0001 | c0005 | t0001 | g0015 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02622 | hp1 | a0002 | c0001 | t0002 | g0038 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0036 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02630 | hp2 | a0002 | c0009 | t0002 | g0156 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0219 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02647 | hp2 | a0001 | c0010 | t0001 | g0089 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0036 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02723 | hp2 | a0002 | c0001 | t0002 | g0038 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02735 | hp1 | a0002 | c0001 | t0002 | g0130 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0211 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02738 | hp1 | a0003 | c0006 | t0001 | g0177 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02809 | hp1 | a0001 | c0007 | t0005 | g0193 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0228 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02895 | hp1 | a0002 | c0001 | t0002 | g0136 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02895 | hp2 | a0002 | c0001 | t0002 | g0100 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0094 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02970 | hp2 | a0001 | c0007 | t0022 | g0195 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0199 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0055 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03041 | hp2 | a0009 | c0024 | t0001 | g0011 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03098 | hp2 | a0002 | c0023 | t0002 | g0057 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03130 | hp1 | a0001 | c0007 | t0023 | g0192 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0227 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03139 | hp2 | a0001 | c0013 | t0001 | g0217 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03209 | hp1 | a0004 | c0008 | t0002 | g0009 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03209 | hp2 | a0003 | c0006 | t0001 | g0049 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0062 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03239 | hp2 | a0001 | c0005 | t0001 | g0037 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03453 | hp2 | a0004 | c0008 | t0002 | g0009 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03486 | hp1 | a0001 | c0005 | t0010 | g0160 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03490 | hp1 | a0003 | c0006 | t0001 | g0178 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03490 | hp2 | a0002 | c0001 | t0002 | g0102 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0174 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03492 | hp2 | a0003 | c0006 | t0001 | g0179 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03516 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0226 | AFR | ESN | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03540 | hp1 | a0002 | c0001 | t0002 | g0101 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0206 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03704 | hp2 | a0002 | c0001 | t0020 | g0021 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0207 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0197 | SAS | PJL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03834 | hp1 | a0002 | c0001 | t0002 | g0097 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0198 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03927 | hp1 | a0003 | c0006 | t0001 | g0171 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03927 | hp2 | a0002 | c0001 | t0002 | g0114 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03942 | hp1 | a0002 | c0001 | t0002 | g0001 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03942 | hp2 | a0003 | c0006 | t0001 | g0051 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG04115 | hp1 | a0002 | c0001 | t0002 | g0153 | SAS | STU | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0163 | SAS | STU | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0205 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG04184 | hp2 | a0003 | c0006 | t0001 | g0024 | SAS | BEB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0159 | AFR | YRI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18522 | hp2 | a0004 | c0008 | t0002 | g0009 | AFR | YRI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18747 | hp1 | a0002 | c0001 | t0002 | g0014 | EAS | CHB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18747 | hp2 | a0002 | c0001 | t0002 | g0091 | EAS | CHB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0017 | AFR | YRI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18906 | hp2 | a0001 | c0007 | t0005 | g0194 | AFR | YRI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18939 | hp1 | a0002 | c0001 | t0015 | g0022 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18939 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18940 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18941 | hp1 | a0002 | c0001 | t0002 | g0120 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18943 | hp2 | a0002 | c0001 | t0002 | g0123 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18944 | hp1 | a0001 | c0007 | t0001 | g0034 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18945 | hp1 | a0002 | c0001 | t0002 | g0040 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18946 | hp1 | a0002 | c0001 | t0002 | g0148 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18949 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18951 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18957 | hp1 | a0002 | c0001 | t0002 | g0107 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18959 | hp2 | a0002 | c0001 | t0002 | g0131 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18960 | hp2 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18961 | hp1 | a0001 | c0007 | t0001 | g0060 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18961 | hp2 | a0002 | c0001 | t0002 | g0142 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18962 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0189 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18965 | hp2 | a0002 | c0001 | t0002 | g0115 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18966 | hp2 | a0002 | c0001 | t0007 | g0157 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18967 | hp1 | a0001 | c0003 | t0018 | g0052 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0190 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18968 | hp2 | a0002 | c0001 | t0002 | g0143 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18970 | hp1 | a0002 | c0001 | t0019 | g0003 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18971 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18972 | hp1 | a0010 | c0015 | t0001 | g0016 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18972 | hp2 | a0002 | c0001 | t0002 | g0145 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18973 | hp1 | a0002 | c0001 | t0014 | g0118 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18974 | hp2 | a0002 | c0001 | t0002 | g0048 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18975 | hp1 | a0002 | c0001 | t0002 | g0106 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18977 | hp1 | a0002 | c0001 | t0002 | g0129 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18978 | hp1 | a0002 | c0001 | t0002 | g0140 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18979 | hp2 | a0002 | c0001 | t0002 | g0047 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18981 | hp1 | a0011 | c0022 | t0001 | g0182 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18981 | hp2 | a0002 | c0001 | t0002 | g0022 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18983 | hp1 | a0002 | c0001 | t0016 | g0119 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18984 | hp1 | a0002 | c0001 | t0002 | g0043 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18985 | hp1 | a0002 | c0001 | t0002 | g0128 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18985 | hp2 | a0002 | c0001 | t0002 | g0146 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18986 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18986 | hp2 | a0001 | c0003 | t0002 | g0093 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18993 | hp1 | a0012 | c0018 | t0002 | g0003 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18994 | hp2 | a0001 | c0007 | t0001 | g0035 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18995 | hp2 | a0002 | c0001 | t0002 | g0132 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18997 | hp1 | a0002 | c0001 | t0002 | g0048 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18997 | hp2 | a0013 | c0025 | t0001 | g0231 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18998 | hp2 | a0002 | c0001 | t0002 | g0111 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19001 | hp1 | a0002 | c0001 | t0002 | g0047 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19001 | hp2 | a0014 | c0027 | t0001 | g0230 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19003 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19005 | hp1 | a0002 | c0001 | t0002 | g0113 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19007 | hp2 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19009 | hp1 | a0002 | c0001 | t0002 | g0042 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19009 | hp2 | a0002 | c0001 | t0007 | g0158 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19011 | hp1 | a0002 | c0001 | t0002 | g0229 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0058 | AFR | LWK | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0175 | AFR | LWK | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0059 | AFR | LWK | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0055 | AFR | LWK | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19054 | hp2 | a0002 | c0001 | t0006 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19056 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19056 | hp2 | a0015 | c0012 | t0001 | g0016 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19057 | hp2 | a0002 | c0001 | t0002 | g0110 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19058 | hp2 | a0002 | c0001 | t0002 | g0124 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19063 | hp2 | a0002 | c0001 | t0002 | g0112 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19064 | hp2 | a0001 | c0007 | t0001 | g0035 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19066 | hp1 | a0002 | c0001 | t0002 | g0138 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19066 | hp2 | a0001 | c0005 | t0001 | g0167 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19068 | hp2 | a0002 | c0001 | t0002 | g0214 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19074 | hp2 | a0001 | c0007 | t0001 | g0092 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19076 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19076 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19078 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19081 | hp2 | a0002 | c0001 | t0002 | g0042 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19082 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19084 | hp1 | a0002 | c0001 | t0002 | g0188 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19086 | hp1 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19086 | hp2 | a0016 | c0021 | t0001 | g0025 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19087 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19088 | hp1 | a0002 | c0001 | t0002 | g0139 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19090 | hp1 | a0002 | c0001 | t0002 | g0104 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19091 | hp1 | a0002 | c0001 | t0002 | g0022 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0081 | AFR | YRI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA19240 | hp2 | a0001 | c0026 | t0001 | g0080 | AFR | YRI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ASW | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20129 | hp2 | a0002 | c0009 | t0002 | g0096 | AFR | ASW | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0204 | EUR | TSI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0183 | EUR | TSI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20805 | hp2 | a0002 | c0001 | t0002 | g0135 | EUR | TSI | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0212 | SAS | GIH | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0209 | SAS | GIH | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01123 | hp1 | a0002 | c0001 | t0002 | g0014 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0170 | AMR | CLM | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0218 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02486 | hp2 | a0003 | c0006 | t0001 | g0007 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02559 | hp1 | a0002 | c0001 | t0002 | g0154 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG02559 | hp2 | a0004 | c0008 | t0002 | g0009 | AFR | ACB | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0224 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0063 | AFR | MSL | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG06807 | hp1 | a0002 | c0001 | t0002 | g0133 | AFR | USA | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| HG06807 | hp2 | a0004 | c0008 | t0002 | g0216 | AFR | USA | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA18955 | hp2 | a0002 | c0001 | t0002 | g0041 | EAS | JPT | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20300 | hp1 | a0001 | c0016 | t0001 | g0186 | AFR | USA | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0200 | AFR | USA | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0208 | AFR | LWK | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| NA21309 | hp2 | a0004 | c0008 | t0002 | g0009 | AFR | LWK | PHC1_chr12_8909509_8946467 | PHC1 | chr12 | 8909509 | 8946467 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8921009 | GC | G | 1 | a0015 | 1 | NA19056.hp2 | frameshift_variant | HIGH | c.252delC | p.Ser85fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 4/15 | 619/5390 | 252/3015 | 84/1004 | INFO_REALIGN_3_PRIME | chr12 | 8921009 | ||
| chr12:8922655 | AG | A | 1 | a0014 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.481delG | p.Val161fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/15 | 848/5390 | 481/3015 | 161/1004 | INFO_REALIGN_3_PRIME | chr12 | 8922655 | ||
| chr12:8922742 | AG | A | 1 | a0011 | 1 | NA18981.hp1 | frameshift_variant | HIGH | c.568delG | p.Val190fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/15 | 935/5390 | 568/3015 | 190/1004 | INFO_REALIGN_3_PRIME | chr12 | 8922742 | ||
| chr12:8930568 | C | T | 1 | a0005 | 2 | HG01168.hp1 HG02300.hp2 |
missense_variant | MODERATE | c.746C>T | p.Ala249Val | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/15 | 1113/5390 | 746/3015 | 249/1004 | chr12 | 8930568 | |||
| chr12:8932691 | T | TC | 1 | a0016 | 1 | NA19086.hp2 | frameshift_variant | HIGH | c.1237dupC | p.Gln413fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 1605/5390 | 1238/3015 | 413/1004 | INFO_REALIGN_3_PRIME | chr12 | 8932691 | ||
| chr12:8932728 | CGCAGCA | C | 1 | a0004 | 6 | HG02559.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.1284_1289delGCAGCA | p.Gln429_Gln430del | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 1651/5390 | 1284/3015 | 428/1004 | INFO_REALIGN_3_PRIME | chr12 | 8932728 | ||
| chr12:8932832 | G | T | 1 | a0007 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1375G>T | p.Val459Phe | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 1742/5390 | 1375/3015 | 459/1004 | chr12 | 8932832 | |||
| chr12:8932856 | C | A | 1 | a0006 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.1399C>A | p.Gln467Lys | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 1766/5390 | 1399/3015 | 467/1004 | chr12 | 8932856 | |||
| chr12:8933006 | G | GT | 1 | a0016 | 1 | NA19086.hp2 | frameshift_variant | HIGH | c.1549_1550insT | p.Ala517fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 1917/5390 | 1550/3015 | 517/1004 | chr12 | 8933006 | |||
| chr12:8933183 | TC | T | 1 | a0010 | 1 | NA18972.hp1 | frameshift_variant | HIGH | c.1729delC | p.Gln577fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 2096/5390 | 1729/3015 | 577/1004 | INFO_REALIGN_3_PRIME | chr12 | 8933183 | ||
| chr12:8933253 | A | AG | 2 | a0012 a0016 |
2 | NA18993.hp1 NA19086.hp2 |
frameshift_variant | HIGH | c.1800dupG | p.Thr601fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 2168/5390 | 1801/3015 | 601/1004 | INFO_REALIGN_3_PRIME | chr12 | 8933253 | ||
| chr12:8933278 | T | TG | 1 | a0016 | 1 | NA19086.hp2 | frameshift_variant | HIGH | c.1825dupG | p.Ala609fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 2193/5390 | 1826/3015 | 609/1004 | INFO_REALIGN_3_PRIME | chr12 | 8933278 | ||
| chr12:8933943 | A | G | 1 | a0009 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1972A>G | p.Met658Val | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 9/15 | 2339/5390 | 1972/3015 | 658/1004 | chr12 | 8933943 | |||
| chr12:8934302 | A | G | 4 | a0002 a0005 a0006 others(1): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
missense_variant | MODERATE | c.2077A>G | p.Thr693Ala | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 10/15 | 2444/5390 | 2077/3015 | 693/1004 | chr12 | 8934302 | |||
| chr12:8934335 | G | A | 2 | a0007 a0008 |
2 | HG01099.hp1 HG01256.hp2 |
missense_variant | MODERATE | c.2110G>A | p.Ala704Thr | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 10/15 | 2477/5390 | 2110/3015 | 704/1004 | chr12 | 8934335 | |||
| chr12:8934471 | C | CT | 1 | a0013 | 1 | NA18997.hp2 | frameshift_variant | HIGH | c.2249dupT | p.Val752fs | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 10/15 | 2617/5390 | 2250/3015 | 750/1004 | INFO_REALIGN_3_PRIME | chr12 | 8934471 | ||
| chr12:8935211 | C | T | 1 | a0004 | 6 | HG02559.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
missense_variant | MODERATE | c.2341C>T | p.Pro781Ser | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/15 | 2708/5390 | 2341/3015 | 781/1004 | chr12 | 8935211 | |||
| chr12:8937932 | G | A | 3 | a0003 a0007 a0008 |
16 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
missense_variant | MODERATE | c.2732G>A | p.Arg911His | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/15 | 3099/5390 | 2732/3015 | 911/1004 | chr12 | 8937932 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8917770 | T | A | 20 | a0001c0003 a0001c0005 a0001c0007 others(17): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
synonymous_variant | LOW | c.93T>A | p.Leu31Leu | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/15 | 460/5390 | 93/3015 | 31/1004 | chr12 | 8917770 | |||
| chr12:8921663 | C | T | 16 | a0001c0003 a0001c0005 a0001c0010 others(13): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
synonymous_variant | LOW | c.369C>T | p.Pro123Pro | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/15 | 736/5390 | 369/3015 | 123/1004 | chr12 | 8921663 | |||
| chr12:8922668 | C | G | 1 | a0001c0026 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.492C>G | p.Thr164Thr | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/15 | 859/5390 | 492/3015 | 164/1004 | chr12 | 8922668 | |||
| chr12:8930740 | A | G | 22 | a0001c0003 a0001c0004 a0001c0005 others(19): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
synonymous_variant | LOW | c.918A>G | p.Arg306Arg | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/15 | 1285/5390 | 918/3015 | 306/1004 | chr12 | 8930740 | |||
| chr12:8932993 | C | T | 1 | a0002c0019 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1536C>T | p.Ala512Ala | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 1903/5390 | 1536/3015 | 512/1004 | chr12 | 8932993 | |||
| chr12:8933302 | T | G | 1 | a0001c0016 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1845T>G | p.Val615Val | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/15 | 2212/5390 | 1845/3015 | 615/1004 | chr12 | 8933302 | |||
| chr12:8933957 | G | A | 7 | a0001c0005 a0001c0013 a0001c0016 others(4): Show |
40 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(37): Show |
synonymous_variant | LOW | c.1986G>A | p.Lys662Lys | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 9/15 | 2353/5390 | 1986/3015 | 662/1004 | chr12 | 8933957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8914541 | C | A | 1 | a0002c0001t0008 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-335C>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/15 | 3137 | chr12 | 8914541 | ||||||
| chr12:8914579 | G | A | 1 | a0001c0004t0009 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-297G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/15 | 3099 | chr12 | 8914579 | ||||||
| chr12:8914609 | G | C | 1 | a0001c0005t0010 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-267G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/15 | 3069 | chr12 | 8914609 | ||||||
| chr12:8939542 | G | A | 1 | a0001c0002t0011 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 83 | chr12 | 8939542 | ||||||
| chr12:8939702 | C | T | 3 | a0001c0007t0005 a0001c0007t0022 a0001c0007t0023 |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 243 | chr12 | 8939702 | ||||||
| chr12:8940038 | G | T | 1 | a0002c0001t0007 | 2 | NA18966.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*579G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 579 | chr12 | 8940038 | ||||||
| chr12:8940039 | T | C | 1 | a0001c0005t0012 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 580 | chr12 | 8940039 | ||||||
| chr12:8940178 | A | G | 3 | a0002c0001t0008 a0002c0001t0020 a0002c0001t0021 |
3 | HG01256.hp1 HG01361.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 719 | chr12 | 8940178 | ||||||
| chr12:8940219 | G | A | 1 | a0001c0003t0013 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 760 | chr12 | 8940219 | ||||||
| chr12:8940342 | A | C | 1 | a0002c0001t0019 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883A>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 883 | chr12 | 8940342 | ||||||
| chr12:8940359 | AAT | A | 1 | a0001c0002t0004 | 4 | HG02486.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*903_*904delAT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 903 | INFO_REALIGN_3_PRIME | chr12 | 8940359 | |||||
| chr12:8940405 | G | A | 25 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0011 others(22): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*946G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 946 | chr12 | 8940405 | ||||||
| chr12:8940488 | C | T | 1 | a0001c0003t0018 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1029C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1029 | chr12 | 8940488 | ||||||
| chr12:8940489 | A | G | 1 | a0001c0004t0017 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1030A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1030 | chr12 | 8940489 | ||||||
| chr12:8940510 | G | GA | 19 | a0001c0003t0002 a0001c0007t0022 a0002c0001t0002 others(16): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1058dupA | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1059 | INFO_REALIGN_3_PRIME | chr12 | 8940510 | |||||
| chr12:8940598 | G | A | 4 | a0001c0007t0005 a0001c0007t0022 a0001c0007t0023 others(1): Show |
7 | HG00408.hp1 HG01109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1139G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1139 | chr12 | 8940598 | ||||||
| chr12:8940665 | T | G | 1 | a0002c0001t0014 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1206T>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1206 | chr12 | 8940665 | ||||||
| chr12:8940669 | A | G | 1 | a0001c0002t0011 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1210 | chr12 | 8940669 | ||||||
| chr12:8941096 | T | C | 1 | a0001c0007t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1637 | chr12 | 8941096 | ||||||
| chr12:8941191 | A | T | 1 | a0002c0001t0021 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1732A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1732 | chr12 | 8941191 | ||||||
| chr12:8941194 | G | A | 1 | a0002c0001t0015 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1735G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1735 | chr12 | 8941194 | ||||||
| chr12:8941290 | A | G | 1 | a0002c0001t0016 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1831A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 15/15 | 1831 | chr12 | 8941290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8914874 | T | C | 1 | a0002c0001t0002g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-49+47T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8914874 | |||||||
| chr12:8915198 | G | T | 2 | a0013c0025t0001g0231 a0014c0027t0001g0230 |
2 | NA18997.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-49+371G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915198 | |||||||
| chr12:8915206 | A | G | 1 | a0002c0001t0002g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-49+379A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915206 | |||||||
| chr12:8915393 | A | T | 13 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0218 others(10): Show |
15 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49+566A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915393 | |||||||
| chr12:8915412 | C | G | 3 | a0001c0013t0001g0217 a0004c0008t0002g0009 a0004c0008t0002g0216 |
7 | HG02559.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+585C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915412 | |||||||
| chr12:8915693 | A | AT | 197 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(194): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-49+872dupT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 8915693 | ||||||
| chr12:8915776 | G | T | 1 | a0001c0002t0001g0084 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-49+949G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915776 | |||||||
| chr12:8915842 | C | G | 1 | a0001c0004t0017g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-49+1015C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915842 | |||||||
| chr12:8915847 | T | A | 5 | a0001c0003t0001g0033 a0001c0003t0001g0085 a0001c0003t0001g0086 others(2): Show |
6 | HG00423.hp2 HG00544.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+1020T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915847 | |||||||
| chr12:8915876 | G | T | 195 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(192): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-49+1049G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8915876 | |||||||
| chr12:8916009 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-49+1182C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916009 | |||||||
| chr12:8916216 | AC | A | 2 | a0001c0003t0002g0093 a0001c0005t0001g0036 |
3 | HG02622.hp2 HG02717.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-49+1390delC | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916216 | |||||||
| chr12:8916217 | C | T | 189 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(186): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-49+1390C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916217 | |||||||
| chr12:8916218 | T | TG | 26 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(23): Show |
35 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-49+1399dupG | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 8916218 | ||||||
| chr12:8916219 | G | T | 1 | a0001c0003t0002g0093 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-49+1392G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916219 | |||||||
| chr12:8916608 | G | A | 211 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(208): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-48-1022G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916608 | |||||||
| chr12:8916646 | T | C | 10 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0218 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-984T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916646 | |||||||
| chr12:8916740 | T | C | 195 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(192): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-48-890T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916740 | |||||||
| chr12:8916787 | C | T | 195 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(192): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-48-843C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8916787 | |||||||
| chr12:8917147 | A | G | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-483A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8917147 | |||||||
| chr12:8917150 | A | G | 1 | a0002c0001t0002g0191 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48-480A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8917150 | |||||||
| chr12:8917386 | C | T | 2 | a0001c0003t0001g0189 a0002c0001t0002g0190 |
2 | NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-48-244C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 1/14 | chr12 | 8917386 | |||||||
| chr12:8917982 | T | C | 198 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(195): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.114+191T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8917982 | |||||||
| chr12:8918048 | C | T | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+257C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918048 | |||||||
| chr12:8918098 | C | T | 3 | a0001c0002t0003g0058 a0001c0002t0003g0059 a0002c0023t0002g0057 |
3 | HG03098.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+307C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918098 | |||||||
| chr12:8918210 | G | T | 2 | a0001c0002t0003g0226 a0001c0002t0003g0227 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.114+419G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918210 | |||||||
| chr12:8918231 | T | G | 1 | a0001c0003t0003g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114+440T>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918231 | |||||||
| chr12:8918484 | T | C | 198 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(195): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.114+693T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918484 | |||||||
| chr12:8918681 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.114+890C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918681 | |||||||
| chr12:8918685 | C | G | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+894C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918685 | |||||||
| chr12:8918723 | G | A | 1 | a0001c0002t0003g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114+932G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918723 | |||||||
| chr12:8918819 | G | A | 2 | a0002c0009t0002g0095 a0002c0009t0002g0096 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.115-937G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918819 | |||||||
| chr12:8918850 | G | A | 1 | a0001c0003t0003g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.115-906G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918850 | |||||||
| chr12:8918916 | T | C | 1 | a0001c0002t0003g0218 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.115-840T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918916 | |||||||
| chr12:8918944 | C | T | 8 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(5): Show |
12 | HG01109.hp2 HG02559.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-812C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918944 | |||||||
| chr12:8918960 | G | A | 3 | a0001c0013t0001g0217 a0004c0008t0002g0009 a0004c0008t0002g0216 |
7 | HG02559.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-796G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918960 | |||||||
| chr12:8918973 | C | T | 1 | a0002c0001t0002g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.115-783C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8918973 | |||||||
| chr12:8919007 | G | A | 1 | a0001c0005t0001g0037 | 2 | HG01081.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.115-749G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919007 | |||||||
| chr12:8919161 | G | A | 1 | a0001c0004t0001g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-595G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919161 | |||||||
| chr12:8919205 | G | A | 1 | a0002c0001t0002g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.115-551G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919205 | |||||||
| chr12:8919245 | G | C | 8 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(5): Show |
12 | HG01109.hp2 HG02559.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-511G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919245 | |||||||
| chr12:8919351 | A | G | 198 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(195): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.115-405A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919351 | |||||||
| chr12:8919566 | C | T | 64 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(61): Show |
93 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.115-190C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919566 | |||||||
| chr12:8919613 | C | T | 1 | a0001c0003t0001g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.115-143C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919613 | |||||||
| chr12:8919734 | G | A | 3 | a0001c0005t0001g0023 a0001c0005t0001g0159 a0001c0005t0010g0160 |
5 | HG02451.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-22G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 2/14 | chr12 | 8919734 | |||||||
| chr12:8919984 | C | T | 1 | a0001c0016t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.225+118C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8919984 | |||||||
| chr12:8920045 | C | T | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+179C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920045 | |||||||
| chr12:8920055 | C | G | 2 | a0002c0001t0007g0157 a0002c0001t0007g0158 |
2 | NA18966.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.225+189C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920055 | |||||||
| chr12:8920094 | G | T | 6 | a0001c0013t0001g0217 a0002c0009t0002g0095 a0002c0009t0002g0096 others(3): Show |
10 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.225+228G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920094 | |||||||
| chr12:8920103 | C | G | 1 | a0002c0001t0007g0158 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.225+237C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920103 | |||||||
| chr12:8920128 | T | C | 1 | a0002c0001t0002g0098 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.225+262T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920128 | |||||||
| chr12:8920225 | A | T | 2 | a0001c0003t0001g0184 a0001c0003t0001g0185 |
2 | NA18952.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.225+359A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920225 | |||||||
| chr12:8920297 | C | T | 1 | a0002c0001t0002g0155 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.225+431C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920297 | |||||||
| chr12:8920397 | G | C | 3 | a0002c0001t0002g0099 a0002c0001t0002g0100 a0002c0001t0002g0101 |
3 | HG02145.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.225+531G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920397 | |||||||
| chr12:8920405 | C | T | 162 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(159): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.225+539C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920405 | |||||||
| chr12:8920450 | G | A | 1 | a0002c0001t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.226-535G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920450 | |||||||
| chr12:8920662 | C | G | 3 | a0002c0001t0002g0099 a0002c0001t0002g0100 a0002c0001t0002g0101 |
3 | HG02145.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.226-323C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920662 | |||||||
| chr12:8920663 | A | G | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-322A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920663 | |||||||
| chr12:8920721 | T | A | 1 | a0001c0003t0003g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.226-264T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920721 | |||||||
| chr12:8920728 | C | T | 1 | a0001c0002t0004g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.226-257C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920728 | |||||||
| chr12:8920741 | A | G | 3 | a0002c0001t0002g0099 a0002c0001t0002g0100 a0002c0001t0002g0101 |
3 | HG02145.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.226-244A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920741 | |||||||
| chr12:8920951 | T | C | 1 | a0002c0023t0002g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226-34T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 3/14 | chr12 | 8920951 | |||||||
| chr12:8921488 | C | T | 1 | a0002c0001t0002g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.307-113C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 4/14 | chr12 | 8921488 | |||||||
| chr12:8921845 | G | A | 3 | a0001c0010t0001g0089 a0001c0010t0001g0090 a0003c0006t0001g0049 |
4 | HG01884.hp1 HG01952.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+95G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8921845 | |||||||
| chr12:8921886 | T | C | 1 | a0002c0001t0002g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.456+136T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8921886 | |||||||
| chr12:8921894 | G | C | 2 | a0001c0002t0003g0226 a0001c0002t0003g0227 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.456+144G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8921894 | |||||||
| chr12:8921938 | C | G | 1 | a0001c0003t0003g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.456+188C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8921938 | |||||||
| chr12:8922065 | C | T | 1 | a0002c0001t0002g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.456+315C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922065 | |||||||
| chr12:8922098 | A | G | 34 | a0001c0002t0003g0226 a0001c0002t0003g0227 a0001c0004t0001g0008 others(31): Show |
43 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.456+348A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922098 | |||||||
| chr12:8922106 | G | A | 89 | a0002c0001t0001g0003 a0002c0001t0001g0121 a0002c0001t0002g0001 others(86): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.456+356G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922106 | |||||||
| chr12:8922110 | G | A | 48 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(45): Show |
63 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.456+360G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922110 | |||||||
| chr12:8922272 | A | C | 1 | a0002c0001t0002g0155 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.457-361A>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922272 | |||||||
| chr12:8922381 | A | T | 9 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0218 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.457-252A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922381 | |||||||
| chr12:8922418 | G | T | 160 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(157): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.457-215G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922418 | |||||||
| chr12:8922428 | CTG | C | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.457-203_457-202del others(2): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 8922428 | ||||||
| chr12:8922444 | A | T | 1 | a0001c0004t0001g0213 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.457-189A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922444 | |||||||
| chr12:8922559 | T | C | 1 | a0002c0001t0002g0038 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.457-74T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 5/14 | chr12 | 8922559 | |||||||
| chr12:8922799 | A | G | 1 | a0002c0023t0002g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.612+11A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8922799 | |||||||
| chr12:8923507 | T | C | 217 | a0001c0002t0003g0029 a0001c0002t0003g0054 a0001c0002t0003g0055 others(214): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.612+719T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923507 | |||||||
| chr12:8923515 | C | A | 1 | a0001c0010t0001g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.612+727C>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923515 | |||||||
| chr12:8923600 | G | A | 1 | a0001c0002t0003g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.612+812G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923600 | |||||||
| chr12:8923687 | A | G | 249 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0011 others(246): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.612+899A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923687 | |||||||
| chr12:8923722 | T | C | 208 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(205): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.612+934T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923722 | |||||||
| chr12:8923755 | G | A | 25 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(22): Show |
35 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.612+967G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923755 | |||||||
| chr12:8923778 | C | G | 1 | a0006c0014t0002g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.612+990C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923778 | |||||||
| chr12:8923822 | T | G | 160 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(157): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.612+1034T>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923822 | |||||||
| chr12:8923829 | C | CA | 179 | a0001c0002t0003g0056 a0001c0003t0001g0004 a0001c0003t0001g0005 others(176): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.612+1058dupA | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8923829 | ||||||
| chr12:8923829 | C | CAA | 9 | a0001c0003t0001g0162 a0001c0003t0001g0163 a0001c0003t0001g0184 others(6): Show |
9 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.612+1057_612+1058d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8923829 | ||||||
| chr12:8923911 | A | G | 32 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(29): Show |
41 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.612+1123A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923911 | |||||||
| chr12:8923919 | G | T | 24 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(21): Show |
33 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.612+1131G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923919 | |||||||
| chr12:8923980 | A | G | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.612+1192A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8923980 | |||||||
| chr12:8924023 | C | G | 2 | a0001c0007t0005g0196 a0001c0007t0022g0195 |
2 | HG01109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.612+1235C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924023 | |||||||
| chr12:8924100 | A | G | 4 | a0002c0001t0002g0022 a0002c0001t0002g0098 a0002c0001t0002g0147 others(1): Show |
5 | HG00544.hp1 HG01943.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+1312A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924100 | |||||||
| chr12:8924144 | T | G | 174 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(171): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.612+1356T>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924144 | |||||||
| chr12:8924200 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.612+1412G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924200 | |||||||
| chr12:8924395 | G | A | 1 | a0001c0002t0003g0056 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.612+1607G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924395 | |||||||
| chr12:8924471 | G | A | 1 | a0011c0022t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.612+1683G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924471 | |||||||
| chr12:8924604 | T | A | 1 | a0002c0001t0002g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.612+1816T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924604 | |||||||
| chr12:8924673 | A | G | 37 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(34): Show |
48 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.612+1885A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924673 | |||||||
| chr12:8924734 | A | G | 33 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(30): Show |
42 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.612+1946A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924734 | |||||||
| chr12:8924763 | G | A | 1 | a0001c0003t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.612+1975G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924763 | |||||||
| chr12:8924866 | G | A | 1 | a0001c0016t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.612+2078G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924866 | |||||||
| chr12:8924901 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.612+2113G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8924901 | |||||||
| chr12:8925192 | CTGTAAAA others(7): Show |
C | 1 | a0001c0003t0001g0181 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.612+2410_612+2423d others(16): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8925192 | ||||||
| chr12:8926107 | G | T | 1 | a0001c0003t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.612+3319G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926107 | |||||||
| chr12:8926276 | T | TG | 32 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(29): Show |
41 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.612+3489dupG | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8926276 | ||||||
| chr12:8926332 | A | G | 214 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(211): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.612+3544A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926332 | |||||||
| chr12:8926356 | C | G | 1 | a0001c0005t0001g0037 | 2 | HG01081.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.612+3568C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926356 | |||||||
| chr12:8926383 | G | A | 3 | a0001c0013t0001g0217 a0004c0008t0002g0009 a0004c0008t0002g0216 |
7 | HG02559.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+3595G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926383 | |||||||
| chr12:8926392 | G | A | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.612+3604G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926392 | |||||||
| chr12:8926462 | C | G | 160 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(157): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.612+3674C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926462 | |||||||
| chr12:8926471 | T | C | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.612+3683T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926471 | |||||||
| chr12:8926476 | C | T | 6 | a0001c0002t0003g0029 a0001c0002t0003g0061 a0001c0002t0004g0029 others(3): Show |
6 | HG02486.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.612+3688C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926476 | |||||||
| chr12:8926491 | A | G | 3 | a0001c0002t0003g0058 a0001c0002t0003g0059 a0002c0023t0002g0057 |
3 | HG03098.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.612+3703A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926491 | |||||||
| chr12:8926680 | C | T | 3 | a0001c0002t0003g0222 a0001c0002t0003g0223 a0001c0002t0003g0224 |
3 | HG01167.hp2 HG01169.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.613-3755C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926680 | |||||||
| chr12:8926693 | C | T | 3 | a0003c0006t0001g0177 a0003c0006t0001g0178 a0003c0006t0001g0179 |
3 | HG02738.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.613-3742C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926693 | |||||||
| chr12:8926870 | G | A | 1 | a0001c0004t0001g0198 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.613-3565G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926870 | |||||||
| chr12:8926887 | C | T | 1 | a0001c0004t0001g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.613-3548C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926887 | |||||||
| chr12:8926902 | C | T | 67 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(64): Show |
96 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.613-3533C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926902 | |||||||
| chr12:8926922 | A | AG | 67 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(64): Show |
96 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.613-3513_613-3512i others(3): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8926922 | |||||||
| chr12:8927029 | G | A | 160 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(157): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.613-3406G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927029 | |||||||
| chr12:8927117 | C | T | 1 | a0001c0003t0001g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.613-3318C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927117 | |||||||
| chr12:8927138 | C | T | 1 | a0002c0001t0002g0146 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.613-3297C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927138 | |||||||
| chr12:8927146 | C | T | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-3289C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927146 | |||||||
| chr12:8927269 | G | T | 1 | a0001c0002t0003g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.613-3166G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927269 | |||||||
| chr12:8927591 | T | C | 24 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(21): Show |
33 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.613-2844T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927591 | |||||||
| chr12:8927846 | G | A | 2 | a0002c0001t0002g0106 a0002c0001t0002g0107 |
2 | NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.613-2589G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927846 | |||||||
| chr12:8927853 | T | TTTTC | 20 | a0001c0002t0001g0011 a0001c0002t0001g0064 a0001c0002t0003g0061 others(17): Show |
27 | HG00408.hp1 HG00639.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.613-2522_613-2519d others(6): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | T | TTTTCTTT others(1): Show |
12 | a0001c0002t0001g0069 a0001c0002t0003g0228 a0002c0001t0002g0042 others(9): Show |
13 | HG01943.hp1 HG01952.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-2526_613-2519d others(10): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | T | TTTTCTTT others(5): Show |
4 | a0001c0002t0004g0062 a0002c0001t0002g0041 a0002c0001t0002g0113 others(1): Show |
5 | HG02129.hp1 HG02129.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-2530_613-2519d others(14): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | T | TTTTCTTT others(9): Show |
2 | a0002c0001t0002g0091 a0002c0001t0002g0110 |
2 | NA18747.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.613-2534_613-2519d others(18): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | TTTTC | T | 25 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0012 others(22): Show |
50 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.613-2522_613-2519d others(6): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | TTTTCTTT others(1): Show |
T | 16 | a0001c0002t0001g0013 a0001c0002t0001g0031 a0001c0002t0001g0078 others(13): Show |
22 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.613-2526_613-2519d others(10): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | TTTTCTTT others(5): Show |
T | 6 | a0001c0002t0001g0079 a0001c0002t0003g0224 a0001c0002t0003g0227 others(3): Show |
6 | HG01168.hp1 HG01261.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.613-2530_613-2519d others(14): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | TTTTCTTT others(9): Show |
T | 4 | a0001c0002t0003g0055 a0001c0003t0001g0181 a0001c0004t0001g0212 others(1): Show |
5 | HG03041.hp1 NA18972.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-2534_613-2519d others(18): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927853 | TTTTCTTT others(13): Show |
T | 1 | a0001c0013t0001g0217 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-2538_613-2519d others(22): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927853 | ||||||
| chr12:8927855 | TTC | T | 6 | a0001c0007t0005g0194 a0001c0007t0005g0196 a0001c0007t0022g0195 others(3): Show |
6 | HG01109.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-2578_613-2577d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927855 | ||||||
| chr12:8927891 | TTCTTTCT others(15): Show |
T | 1 | a0004c0008t0002g0009 | 5 | HG02559.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-2542_613-2521d others(24): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927891 | ||||||
| chr12:8927892 | TCTTTCTT others(14): Show |
T | 1 | a0004c0008t0002g0216 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.613-2542_613-2522d others(23): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927892 | |||||||
| chr12:8927898 | TTTCTTTC others(8): Show |
T | 4 | a0001c0005t0001g0175 a0001c0010t0001g0089 a0001c0010t0001g0090 others(1): Show |
5 | HG01884.hp1 HG01952.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-2534_613-2520d others(17): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927898 | ||||||
| chr12:8927902 | TTTCTTTC others(4): Show |
T | 5 | a0001c0003t0001g0016 a0001c0005t0001g0174 a0010c0015t0001g0016 others(2): Show |
6 | HG03492.hp1 NA18957.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.613-2530_613-2520d others(13): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927902 | ||||||
| chr12:8927903 | TTCTTTCT others(3): Show |
T | 2 | a0001c0003t0001g0052 a0001c0003t0018g0052 |
2 | NA18940.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.613-2530_613-2521d others(12): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927903 | ||||||
| chr12:8927905 | CTTTCTTT others(3): Show |
C | 2 | a0001c0002t0001g0066 a0001c0002t0001g0077 |
2 | HG02145.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.613-2526_613-2517d others(12): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927905 | ||||||
| chr12:8927905 | CTTTCTTT others(4): Show |
C | 2 | a0001c0002t0003g0059 a0001c0004t0001g0209 |
2 | NA19043.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.613-2526_613-2516d others(13): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927905 | ||||||
| chr12:8927906 | TTTCTTTC | T | 20 | a0001c0002t0001g0032 a0001c0002t0003g0056 a0001c0002t0003g0223 others(17): Show |
32 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.613-2526_613-2520d others(9): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927906 | ||||||
| chr12:8927910 | TTTC | T | 17 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0003t0001g0004 others(14): Show |
25 | HG00544.hp2 HG00609.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.613-2522_613-2520d others(5): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927910 | ||||||
| chr12:8927911 | TTC | T | 8 | a0001c0003t0001g0087 a0001c0003t0001g0172 a0001c0005t0001g0015 others(5): Show |
9 | HG01243.hp2 HG01256.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.613-2522_613-2521d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927911 | ||||||
| chr12:8927913 | C | CT | 11 | a0001c0003t0001g0026 a0001c0003t0001g0085 a0001c0003t0001g0162 others(8): Show |
15 | HG01978.hp2 HG02040.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.613-2507dupT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927913 | ||||||
| chr12:8927913 | C | T | 1 | a0001c0013t0001g0217 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-2522C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927913 | |||||||
| chr12:8927913 | CT | C | 9 | a0001c0002t0001g0019 a0001c0003t0001g0169 a0001c0005t0001g0024 others(6): Show |
11 | HG02071.hp2 HG02300.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.613-2507delT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927913 | ||||||
| chr12:8927913 | CTT | C | 6 | a0001c0002t0001g0018 a0001c0002t0003g0219 a0001c0003t0001g0050 others(3): Show |
9 | HG01106.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.613-2508_613-2507d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927913 | ||||||
| chr12:8927914 | T | C | 1 | a0001c0003t0001g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.613-2521T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927914 | |||||||
| chr12:8927914 | T | TTTCTTTC others(4): Show |
2 | a0002c0001t0002g0112 a0003c0006t0001g0166 |
2 | HG01070.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.613-2519_613-2518i others(13): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927914 | ||||||
| chr12:8927914 | T | TTTCTTTC others(8): Show |
1 | a0002c0001t0002g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.613-2519_613-2518i others(17): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927914 | ||||||
| chr12:8927915 | T | TTC | 10 | a0001c0002t0001g0070 a0001c0004t0001g0199 a0001c0005t0001g0167 others(7): Show |
10 | HG00544.hp1 HG02523.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.613-2519_613-2518i others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927915 | ||||||
| chr12:8927915 | T | TTCTTTCT others(3): Show |
3 | a0002c0001t0002g0106 a0002c0001t0002g0111 a0003c0006t0001g0165 |
3 | HG01071.hp1 NA18975.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.613-2519_613-2518i others(12): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927915 | ||||||
| chr12:8927915 | T | TTCTTTCT others(7): Show |
1 | a0002c0001t0002g0040 | 2 | HG02071.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.613-2519_613-2518i others(16): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8927915 | ||||||
| chr12:8927916 | T | TCTTTCTT others(6): Show |
1 | a0002c0001t0002g0108 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.613-2519_613-2518i others(15): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927916 | |||||||
| chr12:8927917 | T | C | 2 | a0001c0007t0022g0195 a0002c0001t0016g0119 |
2 | HG02970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.613-2518T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8927917 | |||||||
| chr12:8928006 | A | G | 1 | a0002c0001t0002g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.613-2429A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928006 | |||||||
| chr12:8928018 | T | C | 1 | a0001c0002t0003g0220 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.613-2417T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928018 | |||||||
| chr12:8928052 | C | T | 1 | a0001c0002t0003g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.613-2383C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928052 | |||||||
| chr12:8928396 | ACT | A | 3 | a0002c0009t0002g0095 a0002c0009t0002g0096 a0002c0009t0002g0156 |
3 | HG02258.hp1 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613-2033_613-2032d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8928396 | ||||||
| chr12:8928422 | AC | A | 91 | a0002c0001t0001g0003 a0002c0001t0001g0121 a0002c0001t0002g0001 others(88): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.613-2011delC | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8928422 | ||||||
| chr12:8928472 | G | A | 1 | a0001c0004t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.613-1963G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928472 | |||||||
| chr12:8928483 | T | C | 3 | a0002c0009t0002g0095 a0002c0009t0002g0096 a0002c0009t0002g0156 |
3 | HG02258.hp1 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613-1952T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928483 | |||||||
| chr12:8928515 | C | T | 3 | a0001c0005t0001g0168 a0001c0005t0001g0173 a0001c0005t0001g0175 |
3 | HG00639.hp1 HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.613-1920C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928515 | |||||||
| chr12:8928567 | T | C | 3 | a0001c0013t0001g0217 a0004c0008t0002g0009 a0004c0008t0002g0216 |
7 | HG02559.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-1868T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928567 | |||||||
| chr12:8928651 | G | A | 1 | a0001c0004t0001g0205 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.613-1784G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928651 | |||||||
| chr12:8928721 | G | C | 3 | a0001c0013t0001g0217 a0004c0008t0002g0009 a0004c0008t0002g0216 |
7 | HG02559.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-1714G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928721 | |||||||
| chr12:8928873 | A | T | 1 | a0001c0002t0003g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.613-1562A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928873 | |||||||
| chr12:8928898 | A | G | 1 | a0002c0001t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.613-1537A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8928898 | |||||||
| chr12:8929220 | C | T | 1 | a0001c0002t0003g0056 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.613-1215C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929220 | |||||||
| chr12:8929283 | C | G | 251 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0010 others(248): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.613-1152C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929283 | |||||||
| chr12:8929397 | C | T | 1 | a0001c0007t0005g0193 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.613-1038C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929397 | |||||||
| chr12:8929399 | G | A | 3 | a0001c0013t0001g0217 a0004c0008t0002g0009 a0004c0008t0002g0216 |
7 | HG02559.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-1036G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929399 | |||||||
| chr12:8929501 | AT | A | 8 | a0001c0002t0001g0078 a0001c0002t0003g0029 a0001c0002t0003g0061 others(5): Show |
8 | HG02056.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-926delT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 8929501 | ||||||
| chr12:8929509 | T | A | 2 | a0001c0003t0003g0094 a0005c0011t0002g0122 |
2 | HG02300.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.613-926T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929509 | |||||||
| chr12:8929516 | A | T | 13 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(10): Show |
15 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.613-919A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929516 | |||||||
| chr12:8929730 | G | A | 1 | a0001c0004t0001g0207 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.613-705G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929730 | |||||||
| chr12:8929951 | C | G | 1 | a0002c0001t0002g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.613-484C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929951 | |||||||
| chr12:8929967 | T | C | 1 | a0002c0019t0002g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.613-468T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929967 | |||||||
| chr12:8929985 | A | G | 35 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(32): Show |
55 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.613-450A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8929985 | |||||||
| chr12:8930018 | T | C | 3 | a0003c0006t0001g0177 a0003c0006t0001g0178 a0003c0006t0001g0179 |
3 | HG02738.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.613-417T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930018 | |||||||
| chr12:8930019 | G | A | 32 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(29): Show |
41 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.613-416G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930019 | |||||||
| chr12:8930047 | G | A | 1 | a0001c0002t0001g0010 | 4 | HG01168.hp2 HG01169.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-388G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930047 | |||||||
| chr12:8930161 | C | T | 10 | a0001c0004t0001g0017 a0001c0004t0001g0027 a0001c0004t0001g0197 others(7): Show |
14 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.613-274C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930161 | |||||||
| chr12:8930168 | A | G | 3 | a0001c0002t0003g0058 a0001c0002t0003g0059 a0002c0023t0002g0057 |
3 | HG03098.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.613-267A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930168 | |||||||
| chr12:8930259 | A | G | 198 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0016 others(195): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.613-176A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930259 | |||||||
| chr12:8930352 | A | G | 1 | a0001c0026t0001g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.613-83A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 6/14 | chr12 | 8930352 | |||||||
| chr12:8930932 | A | G | 2 | a0002c0001t0007g0157 a0002c0001t0007g0158 |
2 | NA18966.hp2 NA19009.hp2 |
splice_region_variant&intron_variant | LOW | c.1105+5A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8930932 | |||||||
| chr12:8931087 | T | C | 1 | a0002c0001t0002g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1105+160T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931087 | |||||||
| chr12:8931421 | C | T | 5 | a0001c0002t0001g0074 a0001c0005t0010g0160 a0002c0019t0002g0152 others(2): Show |
9 | HG01993.hp1 HG02559.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1105+494C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931421 | |||||||
| chr12:8931558 | G | A | 8 | a0001c0002t0001g0031 a0001c0002t0001g0068 a0001c0002t0003g0056 others(5): Show |
9 | HG00738.hp2 HG01261.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1105+631G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931558 | |||||||
| chr12:8931563 | A | G | 5 | a0001c0002t0001g0067 a0001c0002t0001g0070 a0001c0003t0002g0093 others(2): Show |
5 | HG00673.hp1 HG01516.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+636A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931563 | |||||||
| chr12:8931593 | G | A | 1 | a0002c0001t0002g0135 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1105+666G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931593 | |||||||
| chr12:8931779 | T | C | 24 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(21): Show |
33 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1106-784T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931779 | |||||||
| chr12:8931788 | A | T | 1 | a0001c0003t0003g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1106-775A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931788 | |||||||
| chr12:8931938 | T | C | 6 | a0002c0001t0002g0028 a0002c0001t0002g0044 a0002c0001t0002g0046 others(3): Show |
9 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1106-625T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8931938 | |||||||
| chr12:8932017 | C | G | 1 | a0001c0004t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1106-546C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932017 | |||||||
| chr12:8932074 | A | T | 89 | a0001c0002t0001g0071 a0001c0002t0001g0073 a0001c0007t0001g0034 others(86): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1106-489A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932074 | |||||||
| chr12:8932082 | A | G | 164 | a0001c0002t0001g0071 a0001c0002t0001g0073 a0001c0002t0003g0056 others(161): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1106-481A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932082 | |||||||
| chr12:8932088 | T | C | 1 | a0001c0002t0003g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1106-475T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932088 | |||||||
| chr12:8932191 | CAGCCTTT others(4): Show |
C | 60 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(57): Show |
78 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1106-370_1106-360d others(13): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 8932191 | ||||||
| chr12:8932335 | G | A | 103 | a0001c0002t0001g0071 a0001c0002t0001g0073 a0001c0007t0001g0034 others(100): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1106-228G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932335 | |||||||
| chr12:8932503 | G | A | 60 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(57): Show |
78 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1106-60G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932503 | |||||||
| chr12:8932508 | A | G | 1 | a0001c0002t0003g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1106-55A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 7/14 | chr12 | 8932508 | |||||||
| chr12:8933523 | C | T | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1893+173C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/14 | chr12 | 8933523 | |||||||
| chr12:8933644 | A | G | 12 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0218 others(9): Show |
14 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1894-221A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 8/14 | chr12 | 8933644 | |||||||
| chr12:8934087 | A | T | 175 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0056 others(172): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2041+75A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 9/14 | chr12 | 8934087 | |||||||
| chr12:8934230 | T | A | 1 | a0001c0002t0003g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2042-37T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 9/14 | chr12 | 8934230 | |||||||
| chr12:8934485 | G | A | 36 | a0001c0005t0001g0007 a0001c0005t0001g0015 a0001c0005t0001g0023 others(33): Show |
45 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(42): Show |
splice_region_variant&intron_variant | LOW | c.2253+7G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 10/14 | chr12 | 8934485 | |||||||
| chr12:8935037 | A | G | 4 | a0002c0001t0002g0043 a0002c0001t0002g0104 a0002c0001t0002g0131 others(1): Show |
5 | HG02074.hp1 NA18959.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.2254-87A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 10/14 | chr12 | 8935037 | |||||||
| chr12:8935270 | A | T | 36 | a0001c0005t0001g0007 a0001c0005t0001g0015 a0001c0005t0001g0023 others(33): Show |
45 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2368+32A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935270 | |||||||
| chr12:8935310 | ATAG | A | 97 | a0002c0001t0001g0003 a0002c0001t0001g0121 a0002c0001t0002g0001 others(94): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2368+77_2368+79del others(3): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 8935310 | ||||||
| chr12:8935499 | G | A | 7 | a0002c0001t0002g0041 a0002c0001t0002g0091 a0002c0001t0002g0112 others(4): Show |
8 | HG02129.hp2 NA18747.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.2368+261G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935499 | |||||||
| chr12:8935527 | G | A | 5 | a0001c0007t0005g0193 a0001c0007t0005g0194 a0001c0007t0005g0196 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2368+289G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935527 | |||||||
| chr12:8935539 | C | G | 1 | a0001c0002t0001g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2368+301C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935539 | |||||||
| chr12:8935584 | G | A | 1 | a0002c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2368+346G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935584 | |||||||
| chr12:8935587 | A | G | 1 | a0002c0001t0002g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2368+349A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935587 | |||||||
| chr12:8935630 | A | G | 1 | a0001c0003t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2368+392A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935630 | |||||||
| chr12:8935697 | T | A | 1 | a0002c0023t0002g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2368+459T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935697 | |||||||
| chr12:8935768 | A | T | 1 | a0002c0001t0014g0118 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2368+530A>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935768 | |||||||
| chr12:8935768 | AT | A | 2 | a0004c0008t0002g0009 a0004c0008t0002g0216 |
6 | HG02559.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2368+539delT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 8935768 | ||||||
| chr12:8935771 | T | A | 1 | a0001c0002t0003g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2368+533T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935771 | |||||||
| chr12:8935790 | C | T | 2 | a0001c0002t0003g0222 a0001c0002t0003g0223 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2368+552C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8935790 | |||||||
| chr12:8936007 | G | A | 5 | a0001c0002t0001g0012 a0001c0002t0001g0030 a0001c0002t0001g0072 others(2): Show |
9 | NA18941.hp2 NA18955.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.2368+769G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936007 | |||||||
| chr12:8936044 | G | T | 2 | a0001c0005t0001g0159 a0001c0005t0010g0160 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2368+806G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936044 | |||||||
| chr12:8936048 | G | A | 3 | a0002c0001t0002g0047 a0002c0001t0002g0129 a0002c0001t0002g0142 |
4 | NA18961.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2369-808G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936048 | |||||||
| chr12:8936257 | T | C | 156 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(153): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2369-599T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936257 | |||||||
| chr12:8936424 | A | G | 49 | a0001c0004t0001g0008 a0001c0004t0001g0027 a0001c0004t0001g0053 others(46): Show |
64 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.2369-432A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936424 | |||||||
| chr12:8936433 | A | G | 1 | a0001c0003t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2369-423A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936433 | |||||||
| chr12:8936624 | C | G | 1 | a0001c0002t0003g0056 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2369-232C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936624 | |||||||
| chr12:8936649 | G | C | 3 | a0003c0006t0001g0177 a0003c0006t0001g0178 a0003c0006t0001g0179 |
3 | HG02738.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2369-207G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936649 | |||||||
| chr12:8936660 | C | T | 2 | a0002c0001t0002g0114 a0002c0001t0002g0130 |
2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2369-196C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936660 | |||||||
| chr12:8936676 | A | C | 97 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(94): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2369-180A>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | chr12 | 8936676 | |||||||
| chr12:8936749 | T | TG | 97 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(94): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2369-102dupG | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 8936749 | ||||||
| chr12:8937053 | T | C | 2 | a0002c0001t0002g0127 a0002c0001t0002g0136 |
2 | HG00140.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2477+89T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 12/14 | chr12 | 8937053 | |||||||
| chr12:8937133 | T | C | 9 | a0002c0001t0002g0045 a0002c0001t0002g0108 a0002c0001t0002g0109 others(6): Show |
10 | HG01106.hp1 HG01109.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2478-43T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 12/14 | chr12 | 8937133 | |||||||
| chr12:8937142 | A | G | 11 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0218 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2478-34A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 12/14 | chr12 | 8937142 | |||||||
| chr12:8937490 | G | A | 92 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(89): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2628+164G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 13/14 | chr12 | 8937490 | |||||||
| chr12:8937562 | T | C | 1 | a0002c0019t0002g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2628+236T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 13/14 | chr12 | 8937562 | |||||||
| chr12:8937615 | A | G | 2 | a0001c0007t0005g0196 a0001c0007t0022g0195 |
2 | HG01109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2629-214A>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 13/14 | chr12 | 8937615 | |||||||
| chr12:8937624 | T | A | 1 | a0002c0001t0002g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2629-205T>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 13/14 | chr12 | 8937624 | |||||||
| chr12:8937702 | G | A | 2 | a0001c0002t0003g0226 a0001c0002t0003g0227 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2629-127G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 13/14 | chr12 | 8937702 | |||||||
| chr12:8938072 | C | T | 24 | a0001c0004t0001g0008 a0001c0004t0001g0017 a0001c0004t0001g0027 others(21): Show |
33 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.2860+12C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938072 | |||||||
| chr12:8938181 | G | C | 2 | a0004c0008t0002g0009 a0004c0008t0002g0216 |
6 | HG02559.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2860+121G>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938181 | |||||||
| chr12:8938263 | G | A | 92 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(89): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2860+203G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938263 | |||||||
| chr12:8938296 | C | T | 92 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(89): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2860+236C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938296 | |||||||
| chr12:8938445 | C | CT | 92 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(89): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2860+400dupT | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 8938445 | ||||||
| chr12:8938448 | T | C | 1 | a0001c0004t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2860+388T>C | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938448 | |||||||
| chr12:8938520 | G | T | 102 | a0001c0003t0002g0093 a0001c0007t0001g0034 a0001c0007t0001g0035 others(99): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2860+460G>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938520 | |||||||
| chr12:8938597 | CAA | C | 97 | a0001c0003t0002g0093 a0002c0001t0001g0003 a0002c0001t0002g0001 others(94): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2860+539_2860+540d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 8938597 | ||||||
| chr12:8938732 | C | T | 12 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0218 others(9): Show |
14 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2861-573C>T | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938732 | |||||||
| chr12:8938770 | T | G | 1 | a0003c0006t0001g0171 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2861-535T>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938770 | |||||||
| chr12:8938849 | G | A | 1 | a0001c0005t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2861-456G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938849 | |||||||
| chr12:8938859 | CTG | C | 3 | a0002c0009t0002g0095 a0002c0009t0002g0096 a0002c0009t0002g0156 |
3 | HG02258.hp1 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2861-444_2861-443d others(4): Show |
PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 8938859 | ||||||
| chr12:8938974 | C | G | 1 | a0002c0019t0002g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2861-331C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938974 | |||||||
| chr12:8938991 | G | A | 28 | a0001c0002t0003g0029 a0001c0002t0003g0054 a0001c0002t0003g0055 others(25): Show |
30 | HG00738.hp2 HG01109.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.2861-314G>A | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8938991 | |||||||
| chr12:8939230 | C | G | 1 | a0002c0001t0002g0098 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2861-75C>G | PHC1 | ENSG00000111752.11 | transcript | ENST00000544916.6 | protein_coding | 14/14 | chr12 | 8939230 |